Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9411 |
| ensemblid | ENSG00000137962.13 |
| hgncid | 30207 |
| symbol | ARHGAP29 |
| name | Rho GTPase activating protein 29 |
| refseq_nuc | NM_004815.4 |
| refseq_prot | NP_004806.3 |
| ensembl_nuc | ENST00000260526.11 |
| ensembl_prot | ENSP00000260526.6 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 94168905 |
| end | 94237584 |
| strand | - |
| ver | v1.2 |
| region | chr1:94168905-94237584 |
| region5000 | chr1:94163905-94242584 |
| regionname0 | ARHGAP29_chr1_94168905_94237584 |
| regionname5000 | ARHGAP29_chr1_94163905_94242584 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1261 | 333 | 66 | 64 | 157 | 16 | 29 | 121 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | MIAHK others(1256): Show |
chr1 | 94163905 | 94242584 |
| a0002 | 1/0 | 1261 | 16 | 15 | 0 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | MIAHK others(1256): Show |
chr1 | 94163905 | 94242584 |
| a0003 | 0/0 | 1261 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | MIAHK others(1256): Show |
chr1 | 94163905 | 94242584 |
| a0004 | 0/0 | 1261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | MIAHK others(1256): Show |
chr1 | 94163905 | 94242584 |
| a0005 | 0/0 | 1261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | MIAHK others(1256): Show |
chr1 | 94163905 | 94242584 |
| a0006 | 0/0 | 1261 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | MIAHK others(1256): Show |
chr1 | 94163905 | 94242584 |
| a0007 | 0/0 | 1261 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | MIAHK others(1256): Show |
chr1 | 94163905 | 94242584 |
| a0008 | 0/0 | 1261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | MIAHK others(1256): Show |
chr1 | 94163905 | 94242584 |
| a0009 | 0/0 | 1261 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | MIAHK others(1256): Show |
chr1 | 94163905 | 94242584 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3783 | 300 | 61 | 48 | 156 | 11 | 23 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | ATGAT others(3778): Show |
chr1 | 94163905 | 94242584 | ||
| a0001c0002 | 0/0 | 3783 | 28 | 2 | 16 | 0 | 5 | 5 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | ATGAT others(3778): Show |
chr1 | 94163905 | 94242584 | ||
| a0001c0005 | 0/0 | 3783 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | ATGAT others(3778): Show |
chr1 | 94163905 | 94242584 | ||
| a0001c0007 | 0/0 | 3783 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | ATGAT others(3778): Show |
chr1 | 94163905 | 94242584 | ||
| a0001c0009 | 0/0 | 3783 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | ATGAT others(3778): Show |
chr1 | 94163905 | 94242584 | ||
| a0001c0011 | 0/0 | 3783 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | ATGAT others(3778): Show |
chr1 | 94163905 | 94242584 | ||
| a0001c0012 | 0/0 | 3783 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | ATGAT others(3778): Show |
chr1 | 94163905 | 94242584 | ||
| a0002c0003 | 1/0 | 3783 | 15 | 14 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | ATGAT others(3778): Show |
chr1 | 94163905 | 94242584 | ||
| a0002c0015 | 0/0 | 3783 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | ATGAT others(3778): Show |
chr1 | 94163905 | 94242584 | ||
| a0003c0013 | 0/0 | 3783 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | ATGAT others(3778): Show |
chr1 | 94163905 | 94242584 | ||
| a0004c0008 | 0/0 | 3783 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | ATGAT others(3778): Show |
chr1 | 94163905 | 94242584 | ||
| a0005c0014 | 0/0 | 3783 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | ATGAT others(3778): Show |
chr1 | 94163905 | 94242584 | ||
| a0006c0016 | 0/0 | 3783 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | ATGAT others(3778): Show |
chr1 | 94163905 | 94242584 | ||
| a0007c0004 | 0/0 | 3783 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | ATGAT others(3778): Show |
chr1 | 94163905 | 94242584 | ||
| a0008c0010 | 0/0 | 3783 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | ATGAT others(3778): Show |
chr1 | 94163905 | 94242584 | ||
| a0009c0006 | 0/0 | 3783 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | ATGAT others(3778): Show |
chr1 | 94163905 | 94242584 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 8954 | 53 | 2 | 8 | 38 | 1 | 4 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0002 | 0/0 | 8958 | 54 | 7 | 12 | 29 | 2 | 4 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8953): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0003 | 0/1 | 8954 | 44 | 8 | 8 | 20 | 4 | 3 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0004 | 0/0 | 8956 | 36 | 11 | 2 | 23 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8951): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0005 | 0/0 | 8954 | 23 | 1 | 1 | 18 | 1 | 2 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0006 | 0/0 | 8960 | 15 | 2 | 4 | 7 | 2 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8955): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0007 | 0/0 | 8956 | 14 | 3 | 5 | 0 | 0 | 6 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8951): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0009 | 0/0 | 8956 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8951): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0010 | 0/0 | 8934 | 7 | 7 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8929): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0011 | 0/0 | 8958 | 5 | 3 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8953): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0012 | 0/0 | 8956 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8951): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0013 | 0/0 | 8954 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0014 | 0/0 | 8956 | 4 | 0 | 2 | 1 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8951): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0017 | 0/0 | 8954 | 3 | 0 | 1 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0018 | 0/0 | 8952 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8947): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0019 | 0/0 | 8956 | 3 | 1 | 2 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8951): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0020 | 0/0 | 8958 | 3 | 0 | 0 | 3 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8953): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0021 | 0/0 | 8962 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8957): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0022 | 0/0 | 8958 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8953): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0023 | 0/0 | 8956 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8951): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0025 | 0/0 | 8954 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0026 | 0/0 | 8954 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0028 | 0/0 | 8964 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8959): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0029 | 0/0 | 8958 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8953): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0030 | 0/0 | 8958 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8953): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0031 | 0/0 | 8954 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0032 | 0/0 | 8960 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8955): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0034 | 0/0 | 8954 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0035 | 0/0 | 8954 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0036 | 0/0 | 8954 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0037 | 0/0 | 8956 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8951): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0038 | 0/0 | 8954 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0039 | 0/0 | 8960 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8955): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0041 | 0/0 | 8952 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8947): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0042 | 0/0 | 8956 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8951): Show |
chr1 | 94163905 | 94242584 |
| a0001c0001t0043 | 0/0 | 8952 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8947): Show |
chr1 | 94163905 | 94242584 |
| a0001c0002t0001 | 0/0 | 8954 | 18 | 2 | 9 | 0 | 3 | 4 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0001c0002t0009 | 0/0 | 8956 | 5 | 0 | 4 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8951): Show |
chr1 | 94163905 | 94242584 |
| a0001c0002t0016 | 0/0 | 8954 | 3 | 0 | 1 | 0 | 2 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0001c0002t0027 | 0/0 | 8954 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0001c0002t0033 | 0/0 | 8958 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8953): Show |
chr1 | 94163905 | 94242584 |
| a0001c0005t0013 | 0/0 | 8954 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0001c0007t0001 | 0/0 | 8954 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0001c0009t0003 | 0/0 | 8954 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0001c0011t0040 | 0/0 | 8956 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8951): Show |
chr1 | 94163905 | 94242584 |
| a0001c0012t0007 | 0/0 | 8956 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8951): Show |
chr1 | 94163905 | 94242584 |
| a0002c0003t0008 | 1/0 | 8952 | 9 | 8 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8947): Show |
chr1 | 94163905 | 94242584 |
| a0002c0003t0015 | 0/0 | 8952 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8947): Show |
chr1 | 94163905 | 94242584 |
| a0002c0003t0024 | 0/0 | 8952 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8947): Show |
chr1 | 94163905 | 94242584 |
| a0002c0003t0044 | 0/0 | 8952 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8947): Show |
chr1 | 94163905 | 94242584 |
| a0002c0015t0024 | 0/0 | 8952 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8947): Show |
chr1 | 94163905 | 94242584 |
| a0003c0013t0006 | 0/0 | 8960 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8955): Show |
chr1 | 94163905 | 94242584 |
| a0004c0008t0003 | 0/0 | 8954 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0005c0014t0011 | 0/0 | 8958 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8953): Show |
chr1 | 94163905 | 94242584 |
| a0006c0016t0016 | 0/0 | 8954 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0007c0004t0001 | 0/0 | 8954 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| a0008c0010t0022 | 0/0 | 8958 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8953): Show |
chr1 | 94163905 | 94242584 |
| a0009c0006t0001 | 0/0 | 8954 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | AGTGG others(8949): Show |
chr1 | 94163905 | 94242584 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0023 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0005g0001 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0005g0005 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0005g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0005g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0006g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0006g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0006g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0006g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0006g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0007g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0007g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0007g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0007g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0007g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0007g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0007g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0007g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0007g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0007g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0007g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0007g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0009g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0009g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0009g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0010g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0010g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0010g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0010g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0010g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0011g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0011g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0011g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0011g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0011g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0012g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0012g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0012g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0012g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0012g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0013g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0013g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0013g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0014g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0014g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0014g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0017g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0017g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0017g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0018g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0018g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0018g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0019g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0019g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0020g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0020g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0021g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0021g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0022g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0023g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0023g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0025g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0025g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0026g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0028g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0029g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0030g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0031g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0032g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0034g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0035g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0036g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0037g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0038g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0039g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0041g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0042g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0001t0043g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0009g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0009g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0009g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0009g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0009g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0016g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0016g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0016g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0027g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0002t0033g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0005t0013g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0007t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0009t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0011t0040g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0001c0012t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0002c0003t0008g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0002c0003t0008g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0002c0003t0008g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0002c0003t0008g0295 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0002c0003t0008g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0002c0003t0008g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0002c0003t0008g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0002c0003t0008g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0002c0003t0015g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0002c0003t0015g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0002c0003t0015g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0002c0003t0015g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0002c0003t0024g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0002c0003t0044g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0002c0015t0024g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0003c0013t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0004c0008t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0005c0014t0011g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0006c0016t0016g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0007c0004t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0008c0010t0022g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| a0009c0006t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0016 | g0163 | EUR | GBR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | GBR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0026 | EUR | FIN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0057 | EUR | FIN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0157 | EUR | FIN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00323 | hp2 | a0001 | c0001 | t0014 | g0024 | EUR | FIN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00423 | hp1 | a0001 | c0001 | t0005 | g0130 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00423 | hp2 | a0003 | c0013 | t0006 | g0077 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0279 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00544 | hp1 | a0001 | c0001 | t0013 | g0280 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0225 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00597 | hp1 | a0001 | c0001 | t0011 | g0229 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00597 | hp2 | a0001 | c0001 | t0020 | g0030 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00621 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | CHS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0159 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00639 | hp2 | a0001 | c0001 | t0014 | g0306 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0063 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00733 | hp1 | a0001 | c0002 | t0027 | g0151 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00735 | hp1 | a0001 | c0002 | t0033 | g0158 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0112 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01069 | hp1 | a0001 | c0001 | t0006 | g0060 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0172 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0175 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0110 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01074 | hp1 | a0001 | c0001 | t0014 | g0024 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0310 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01106 | hp1 | a0001 | c0002 | t0009 | g0160 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01109 | hp1 | a0001 | c0001 | t0007 | g0104 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01109 | hp2 | a0001 | c0002 | t0009 | g0152 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01168 | hp1 | a0001 | c0002 | t0009 | g0150 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0161 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01243 | hp2 | a0001 | c0001 | t0025 | g0248 | AMR | PUR | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01256 | hp1 | a0001 | c0001 | t0006 | g0065 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01256 | hp2 | a0001 | c0001 | t0023 | g0179 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01257 | hp1 | a0001 | c0001 | t0019 | g0182 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01258 | hp1 | a0001 | c0001 | t0006 | g0058 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01258 | hp2 | a0001 | c0001 | t0019 | g0017 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01358 | hp1 | a0001 | c0001 | t0017 | g0252 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0166 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01433 | hp1 | a0001 | c0002 | t0009 | g0154 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0146 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0149 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0243 | EUR | IBS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01516 | hp1 | a0001 | c0001 | t0006 | g0059 | EUR | IBS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01516 | hp2 | a0001 | c0002 | t0016 | g0162 | EUR | IBS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01517 | hp1 | a0001 | c0001 | t0006 | g0062 | EUR | IBS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01884 | hp2 | a0001 | c0001 | t0012 | g0263 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0219 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0138 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01928 | hp1 | a0001 | c0001 | t0004 | g0208 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01943 | hp1 | a0001 | c0001 | t0005 | g0119 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01952 | hp1 | a0001 | c0001 | t0007 | g0037 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0271 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01981 | hp2 | a0001 | c0001 | t0028 | g0097 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01993 | hp1 | a0001 | c0001 | t0007 | g0038 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0167 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02015 | hp2 | a0001 | c0001 | t0014 | g0220 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02040 | hp2 | a0001 | c0001 | t0023 | g0255 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02056 | hp1 | a0001 | c0001 | t0009 | g0190 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02056 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02074 | hp1 | a0001 | c0001 | t0017 | g0265 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02135 | hp1 | a0001 | c0001 | t0006 | g0251 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02145 | hp1 | a0001 | c0001 | t0036 | g0031 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0311 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0134 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0227 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CDX | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02165 | hp2 | a0001 | c0001 | t0034 | g0191 | EAS | CDX | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0148 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0136 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02258 | hp1 | a0004 | c0008 | t0003 | g0262 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0103 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0105 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02280 | hp2 | a0005 | c0014 | t0011 | g0215 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | PEL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02451 | hp1 | a0001 | c0001 | t0012 | g0264 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02451 | hp2 | a0001 | c0001 | t0019 | g0017 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02523 | hp1 | a0001 | c0001 | t0031 | g0118 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | KHV | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02572 | hp2 | a0001 | c0001 | t0035 | g0140 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0308 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02630 | hp2 | a0001 | c0001 | t0022 | g0041 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0206 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0301 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02698 | hp1 | a0001 | c0001 | t0026 | g0128 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02698 | hp2 | a0001 | c0002 | t0009 | g0153 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02717 | hp2 | a0001 | c0001 | t0021 | g0309 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02723 | hp1 | a0002 | c0003 | t0015 | g0250 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02723 | hp2 | a0001 | c0001 | t0010 | g0238 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02735 | hp1 | a0001 | c0001 | t0007 | g0108 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0261 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0106 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0221 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02809 | hp2 | a0001 | c0012 | t0007 | g0184 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02886 | hp1 | a0001 | c0001 | t0032 | g0213 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02895 | hp2 | a0001 | c0001 | t0018 | g0234 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0214 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02896 | hp2 | a0002 | c0003 | t0008 | g0296 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02897 | hp1 | a0001 | c0001 | t0011 | g0216 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02897 | hp2 | a0001 | c0001 | t0018 | g0235 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0016 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02922 | hp2 | a0002 | c0003 | t0008 | g0298 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0223 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0274 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02970 | hp1 | a0002 | c0003 | t0015 | g0052 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0236 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0275 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02976 | hp2 | a0002 | c0003 | t0044 | g0297 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03041 | hp2 | a0001 | c0001 | t0012 | g0269 | AFR | GWD | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03098 | hp2 | a0002 | c0003 | t0015 | g0249 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0053 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0307 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03139 | hp1 | a0002 | c0003 | t0008 | g0293 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0303 | AFR | ESN | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0226 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03209 | hp2 | a0002 | c0003 | t0024 | g0244 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0107 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03225 | hp2 | a0001 | c0001 | t0038 | g0141 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03453 | hp1 | a0001 | c0001 | t0010 | g0137 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0278 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0142 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03486 | hp2 | a0002 | c0003 | t0008 | g0300 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03491 | hp1 | a0001 | c0001 | t0007 | g0109 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03491 | hp2 | a0001 | c0001 | t0025 | g0247 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03579 | hp1 | a0001 | c0001 | t0012 | g0272 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03579 | hp2 | a0002 | c0003 | t0008 | g0299 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0147 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0292 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03710 | hp2 | a0006 | c0016 | t0016 | g0155 | SAS | PJL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0156 | SAS | BEB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03831 | hp2 | a0001 | c0001 | t0043 | g0290 | SAS | BEB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0005 | SAS | BEB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0240 | SAS | BEB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG04115 | hp1 | a0001 | c0001 | t0007 | g0036 | SAS | STU | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG04115 | hp2 | a0001 | c0007 | t0001 | g0045 | SAS | STU | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0026 | SAS | BEB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0258 | SAS | STU | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG04204 | hp2 | a0001 | c0001 | t0007 | g0113 | SAS | STU | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG04228 | hp1 | a0001 | c0001 | t0007 | g0035 | SAS | STU | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0120 | SAS | STU | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0016 | AFR | YRI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | YRI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18612 | hp1 | a0007 | c0004 | t0001 | g0181 | EAS | CHB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0125 | EAS | CHB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18906 | hp1 | a0002 | c0003 | t0015 | g0051 | AFR | YRI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0207 | AFR | YRI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18941 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18943 | hp1 | a0001 | c0001 | t0013 | g0254 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18943 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18952 | hp2 | a0001 | c0001 | t0021 | g0089 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18965 | hp1 | a0001 | c0001 | t0006 | g0081 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18966 | hp1 | a0001 | c0001 | t0009 | g0203 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18967 | hp1 | a0001 | c0001 | t0004 | g0230 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18970 | hp2 | a0001 | c0001 | t0006 | g0093 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18973 | hp1 | a0001 | c0001 | t0030 | g0075 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18975 | hp1 | a0001 | c0005 | t0013 | g0253 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18983 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18984 | hp1 | a0001 | c0001 | t0006 | g0070 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0209 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18994 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18995 | hp2 | a0001 | c0001 | t0017 | g0266 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0218 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19000 | hp1 | a0001 | c0001 | t0006 | g0096 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19000 | hp2 | a0001 | c0001 | t0011 | g0183 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19005 | hp2 | a0001 | c0001 | t0005 | g0127 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0126 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19009 | hp2 | a0001 | c0001 | t0029 | g0056 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19011 | hp2 | a0001 | c0001 | t0006 | g0082 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19030 | hp1 | a0002 | c0003 | t0008 | g0294 | AFR | LWK | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19030 | hp2 | a0001 | c0011 | t0040 | g0180 | AFR | LWK | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | LWK | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19043 | hp2 | a0008 | c0010 | t0022 | g0040 | AFR | LWK | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19054 | hp1 | a0009 | c0006 | t0001 | g0187 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19056 | hp1 | a0001 | c0001 | t0020 | g0312 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19066 | hp1 | a0001 | c0001 | t0006 | g0091 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19067 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19067 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19076 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19081 | hp1 | a0001 | c0001 | t0009 | g0202 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19081 | hp2 | a0001 | c0001 | t0013 | g0256 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19082 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0010 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19087 | hp2 | a0001 | c0001 | t0005 | g0124 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19089 | hp2 | a0001 | c0001 | t0039 | g0083 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19090 | hp2 | a0001 | c0001 | t0020 | g0030 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0117 | AFR | YRI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0277 | AFR | YRI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0068 | EUR | TSI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0164 | EUR | TSI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0001 | EUR | TSI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0006 | EUR | TSI | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA20905 | hp1 | a0001 | c0001 | t0042 | g0291 | SAS | GIH | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | GIH | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG01123 | hp2 | a0001 | c0002 | t0016 | g0145 | AMR | CLM | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02109 | hp1 | a0001 | c0009 | t0003 | g0276 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02109 | hp2 | a0002 | c0003 | t0008 | g0028 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02486 | hp1 | a0001 | c0001 | t0018 | g0139 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02486 | hp2 | a0001 | c0001 | t0037 | g0305 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | ACB | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0288 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG03471 | hp2 | a0001 | c0001 | t0041 | g0116 | AFR | MSL | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0237 | AFR | USA | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| HG06807 | hp2 | a0002 | c0003 | t0008 | g0028 | AFR | USA | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0245 | AFR | USA | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0289 | AFR | USA | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | LWK | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| NA21309 | hp2 | a0002 | c0015 | t0024 | g0185 | AFR | LWK | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0144 | REF | REF | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0008 | g0295 | REF | REF | ARHGAP29_chr1_94163905_94242584 | ARHGAP29 | chr1 | 94163905 | 94242584 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:94173891 | C | T | 8 | a0001 a0003 a0004 others(5): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
missense_variant | MODERATE | c.3764G>A | p.Gly1255Asp | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3966/8952 | 3764/3786 | 1255/1261 | chr1 | 94173891 | |||
| chr1:94174051 | C | A | 1 | a0003 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.3604G>T | p.Val1202Leu | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3806/8952 | 3604/3786 | 1202/1261 | chr1 | 94174051 | |||
| chr1:94174698 | A | G | 1 | a0008 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.2957T>C | p.Ile986Thr | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3159/8952 | 2957/3786 | 986/1261 | chr1 | 94174698 | |||
| chr1:94179812 | C | T | 1 | a0004 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.2393G>A | p.Arg798Gln | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/23 | 2595/8952 | 2393/3786 | 798/1261 | chr1 | 94179812 | |||
| chr1:94185416 | G | A | 1 | a0005 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.1846C>T | p.Arg616Cys | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 17/23 | 2048/8952 | 1846/3786 | 616/1261 | chr1 | 94185416 | |||
| chr1:94201749 | C | T | 1 | a0009 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.1252G>A | p.Val418Ile | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/23 | 1454/8952 | 1252/3786 | 418/1261 | chr1 | 94201749 | |||
| chr1:94205174 | T | C | 1 | a0006 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.584A>G | p.Asp195Gly | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/23 | 786/8952 | 584/3786 | 195/1261 | chr1 | 94205174 | |||
| chr1:94220347 | C | T | 1 | a0007 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.251G>A | p.Arg84His | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/23 | 453/8952 | 251/3786 | 84/1261 | chr1 | 94220347 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:94174289 | A | T | 1 | a0002c0015 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.3366T>A | p.Thr1122Thr | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3568/8952 | 3366/3786 | 1122/1261 | chr1 | 94174289 | |||
| chr1:94174310 | C | T | 1 | a0001c0012 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.3345G>A | p.Gly1115Gly | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3547/8952 | 3345/3786 | 1115/1261 | chr1 | 94174310 | |||
| chr1:94174373 | A | G | 1 | a0001c0011 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.3282T>C | p.Thr1094Thr | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3484/8952 | 3282/3786 | 1094/1261 | chr1 | 94174373 | |||
| chr1:94177640 | C | T | 1 | a0001c0009 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.2877G>A | p.Ala959Ala | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/23 | 3079/8952 | 2877/3786 | 959/1261 | chr1 | 94177640 | |||
| chr1:94177975 | T | C | 2 | a0001c0002 a0006c0016 |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(26): Show |
synonymous_variant | LOW | c.2673A>G | p.Gln891Gln | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 21/23 | 2875/8952 | 2673/3786 | 891/1261 | chr1 | 94177975 | |||
| chr1:94186506 | T | C | 1 | a0002c0015 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1773A>G | p.Ser591Ser | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 16/23 | 1975/8952 | 1773/3786 | 591/1261 | chr1 | 94186506 | |||
| chr1:94190075 | A | C | 1 | a0001c0007 | 1 | HG04115.hp2 | synonymous_variant | LOW | c.1290T>G | p.Val430Val | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 13/23 | 1492/8952 | 1290/3786 | 430/1261 | chr1 | 94190075 | |||
| chr1:94205669 | A | G | 1 | a0001c0005 | 1 | NA18975.hp1 | synonymous_variant | LOW | c.525T>C | p.Val175Val | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 6/23 | 727/8952 | 525/3786 | 175/1261 | chr1 | 94205669 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:94168920 | G | A | 3 | a0001c0001t0010 a0001c0001t0041 a0001c0011t0040 |
9 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4949C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4949 | chr1 | 94168920 | ||||||
| chr1:94169054 | C | T | 1 | a0001c0001t0035 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4815G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4815 | chr1 | 94169054 | ||||||
| chr1:94169106 | A | C | 1 | a0001c0011t0040 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4763T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4763 | chr1 | 94169106 | ||||||
| chr1:94169108 | G | A | 1 | a0001c0001t0018 | 3 | HG02486.hp1 HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4761C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4761 | chr1 | 94169108 | ||||||
| chr1:94169144 | C | T | 1 | a0001c0001t0010 | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4725G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4725 | chr1 | 94169144 | ||||||
| chr1:94169407 | C | A | 17 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(14): Show |
124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*4462G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4462 | chr1 | 94169407 | ||||||
| chr1:94169472 | G | A | 17 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(14): Show |
124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*4397C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4397 | chr1 | 94169472 | ||||||
| chr1:94169609 | TGAC | T | 1 | a0001c0001t0010 | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4257_*4259delGTC | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4257 | chr1 | 94169609 | ||||||
| chr1:94169637 | C | T | 2 | a0001c0001t0017 a0002c0003t0044 |
4 | HG01358.hp1 HG02074.hp1 HG02976.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4232G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4232 | chr1 | 94169637 | ||||||
| chr1:94169638 | G | A | 1 | a0001c0001t0041 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4231C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4231 | chr1 | 94169638 | ||||||
| chr1:94169706 | T | C | 3 | a0001c0001t0010 a0001c0001t0041 a0001c0011t0040 |
9 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4163A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4163 | chr1 | 94169706 | ||||||
| chr1:94169793 | G | T | 1 | a0001c0001t0029 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4076C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4076 | chr1 | 94169793 | ||||||
| chr1:94170370 | C | G | 1 | a0001c0001t0010 | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3499G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3499 | chr1 | 94170370 | ||||||
| chr1:94170430 | T | C | 24 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0009 others(21): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*3439A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3439 | chr1 | 94170430 | ||||||
| chr1:94170498 | A | C | 1 | a0001c0011t0040 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3371T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3371 | chr1 | 94170498 | ||||||
| chr1:94170615 | T | C | 1 | a0001c0001t0014 | 4 | HG00323.hp2 HG00639.hp2 HG01074.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3254A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3254 | chr1 | 94170615 | ||||||
| chr1:94170703 | A | T | 10 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0013 others(7): Show |
63 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*3166T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 3166 | chr1 | 94170703 | ||||||
| chr1:94171133 | T | C | 2 | a0001c0001t0042 a0001c0001t0043 |
2 | HG03831.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2736A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 2736 | chr1 | 94171133 | ||||||
| chr1:94171160 | G | C | 1 | a0001c0001t0030 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2709C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 2709 | chr1 | 94171160 | ||||||
| chr1:94171231 | T | C | 1 | a0001c0001t0031 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2638A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 2638 | chr1 | 94171231 | ||||||
| chr1:94171280 | A | G | 12 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(9): Show |
97 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2589T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 2589 | chr1 | 94171280 | ||||||
| chr1:94171298 | A | G | 1 | a0001c0001t0034 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2571T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 2571 | chr1 | 94171298 | ||||||
| chr1:94171436 | T | A | 1 | a0002c0003t0015 | 4 | HG02723.hp1 HG02970.hp1 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2433A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 2433 | chr1 | 94171436 | ||||||
| chr1:94171502 | C | T | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0009 others(22): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*2367G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 2367 | chr1 | 94171502 | ||||||
| chr1:94171520 | G | A | 1 | a0001c0001t0041 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2349C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 2349 | chr1 | 94171520 | ||||||
| chr1:94171759 | C | G | 1 | a0001c0011t0040 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2110G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 2110 | chr1 | 94171759 | ||||||
| chr1:94172164 | G | C | 1 | a0001c0001t0012 | 5 | HG01884.hp2 HG02451.hp1 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1705C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1705 | chr1 | 94172164 | ||||||
| chr1:94172612 | G | GAT | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(19): Show |
162 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*1255_*1256dupAT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1256 | chr1 | 94172612 | ||||||
| chr1:94172612 | G | GATAT | 12 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0009 others(9): Show |
76 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1253_*1256dupATAT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1256 | chr1 | 94172612 | ||||||
| chr1:94172612 | G | GATATAT | 9 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0020 others(6): Show |
68 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1251_*1256dupATAT others(2): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1256 | chr1 | 94172612 | ||||||
| chr1:94172612 | G | GATATATA others(1): Show |
4 | a0001c0001t0006 a0001c0001t0032 a0001c0001t0039 others(1): Show |
18 | HG00423.hp2 HG00642.hp1 HG01069.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1249_*1256dupATAT others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1256 | chr1 | 94172612 | ||||||
| chr1:94172612 | G | GATATATA others(3): Show |
1 | a0001c0001t0021 | 2 | HG02717.hp2 NA18952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1247_*1256dupATAT others(6): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1256 | chr1 | 94172612 | ||||||
| chr1:94172612 | G | GATATATA others(5): Show |
1 | a0001c0001t0028 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1245_*1256dupATAT others(8): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1256 | chr1 | 94172612 | ||||||
| chr1:94172612 | GATATATA others(5): Show |
G | 1 | a0001c0001t0010 | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1245_*1256delATAT others(8): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1245 | chr1 | 94172612 | ||||||
| chr1:94172633 | T | A | 2 | a0001c0001t0042 a0001c0001t0043 |
2 | HG03831.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1236A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1236 | chr1 | 94172633 | ||||||
| chr1:94172651 | C | T | 1 | a0001c0001t0038 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1218G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1218 | chr1 | 94172651 | ||||||
| chr1:94172720 | T | C | 2 | a0001c0002t0016 a0006c0016t0016 |
4 | HG00140.hp1 HG01123.hp2 HG01516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1149A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1149 | chr1 | 94172720 | ||||||
| chr1:94172792 | T | C | 1 | a0001c0001t0037 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1077A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1077 | chr1 | 94172792 | ||||||
| chr1:94172817 | T | C | 1 | a0001c0001t0038 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1052A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1052 | chr1 | 94172817 | ||||||
| chr1:94172883 | A | C | 15 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(12): Show |
122 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*986T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 986 | chr1 | 94172883 | ||||||
| chr1:94172891 | C | T | 2 | a0001c0001t0013 a0001c0005t0013 |
4 | HG00544.hp1 NA18943.hp1 NA18975.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*978G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 978 | chr1 | 94172891 | ||||||
| chr1:94173155 | C | T | 17 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(14): Show |
124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*714G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 714 | chr1 | 94173155 | ||||||
| chr1:94173172 | T | C | 1 | a0001c0001t0019 | 3 | HG01257.hp1 HG01258.hp2 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*697A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 697 | chr1 | 94173172 | ||||||
| chr1:94173202 | G | T | 1 | a0001c0011t0040 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*667C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 667 | chr1 | 94173202 | ||||||
| chr1:94173233 | T | A | 1 | a0001c0001t0039 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*636A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 636 | chr1 | 94173233 | ||||||
| chr1:94173408 | C | A | 5 | a0001c0001t0010 a0001c0001t0041 a0001c0001t0042 others(2): Show |
11 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*461G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 461 | chr1 | 94173408 | ||||||
| chr1:94173431 | G | A | 1 | a0001c0001t0025 | 2 | HG01243.hp2 HG03491.hp2 |
3_prime_UTR_variant | MODIFIER | c.*438C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 438 | chr1 | 94173431 | ||||||
| chr1:94173445 | C | T | 1 | a0001c0002t0027 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*424G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 424 | chr1 | 94173445 | ||||||
| chr1:94173545 | A | G | 1 | a0001c0001t0026 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*324T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 324 | chr1 | 94173545 | ||||||
| chr1:94173781 | A | G | 56 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(53): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
3_prime_UTR_variant | MODIFIER | c.*88T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 88 | chr1 | 94173781 | ||||||
| chr1:94173832 | CACA | C | 1 | a0001c0001t0010 | 7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*34_*36delTGT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 34 | chr1 | 94173832 | ||||||
| chr1:94237571 | G | C | 1 | a0001c0001t0020 | 3 | HG00597.hp2 NA19056.hp1 NA19090.hp2 |
5_prime_UTR_variant | MODIFIER | c.-189C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/23 | 5960 | chr1 | 94237571 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:94174838 | A | G | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2906-89T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94174838 | |||||||
| chr1:94174996 | C | T | 1 | a0001c0001t0004g0206 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2906-247G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94174996 | |||||||
| chr1:94175169 | C | T | 1 | a0001c0001t0003g0046 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2906-420G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175169 | |||||||
| chr1:94175233 | T | C | 2 | a0001c0001t0004g0209 a0001c0001t0011g0183 |
2 | NA18989.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.2906-484A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175233 | |||||||
| chr1:94175239 | T | C | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2906-490A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175239 | |||||||
| chr1:94175267 | C | G | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2906-518G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175267 | |||||||
| chr1:94175293 | C | T | 1 | a0001c0001t0002g0011 | 2 | HG01074.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.2906-544G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175293 | |||||||
| chr1:94175332 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(46): Show |
61 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.2906-583C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175332 | |||||||
| chr1:94175375 | A | C | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2906-626T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175375 | |||||||
| chr1:94175434 | G | T | 1 | a0001c0001t0007g0104 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2906-685C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175434 | |||||||
| chr1:94175524 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2906-775G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175524 | |||||||
| chr1:94175641 | A | C | 296 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(293): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.2906-892T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175641 | |||||||
| chr1:94175689 | G | C | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2906-940C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175689 | |||||||
| chr1:94175858 | C | T | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2906-1109G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94175858 | |||||||
| chr1:94176007 | G | C | 1 | a0001c0001t0038g0141 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2906-1258C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94176007 | |||||||
| chr1:94176122 | A | G | 1 | a0002c0003t0024g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2906-1373T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94176122 | |||||||
| chr1:94176701 | G | A | 1 | a0001c0001t0036g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2905+911C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94176701 | |||||||
| chr1:94176720 | G | A | 1 | a0001c0001t0003g0173 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2905+892C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94176720 | |||||||
| chr1:94176721 | C | G | 1 | a0001c0001t0003g0173 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2905+891G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94176721 | |||||||
| chr1:94176887 | G | A | 1 | a0001c0001t0003g0277 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2905+725C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94176887 | |||||||
| chr1:94176939 | T | C | 1 | a0001c0001t0038g0141 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2905+673A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94176939 | |||||||
| chr1:94177107 | G | A | 1 | a0001c0001t0036g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2905+505C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94177107 | |||||||
| chr1:94177142 | GTGTTTAA others(9): Show |
G | 1 | a0001c0001t0004g0053 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2905+454_2905+469d others(18): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94177142 | |||||||
| chr1:94177179 | C | T | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2905+433G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94177179 | |||||||
| chr1:94177199 | A | T | 3 | a0001c0001t0004g0032 a0001c0001t0004g0053 a0001c0001t0004g0207 |
3 | HG02559.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2905+413T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94177199 | |||||||
| chr1:94177230 | T | C | 286 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(283): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.2905+382A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94177230 | |||||||
| chr1:94177288 | C | T | 3 | a0001c0001t0004g0100 a0001c0001t0004g0218 a0001c0001t0004g0230 |
3 | NA18949.hp2 NA18967.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.2905+324G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94177288 | |||||||
| chr1:94177475 | T | C | 1 | a0001c0001t0005g0120 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2905+137A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | 94177475 | |||||||
| chr1:94178224 | G | A | 1 | a0001c0001t0021g0089 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2481-57C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94178224 | |||||||
| chr1:94178419 | G | GA | 3 | a0001c0001t0003g0027 a0001c0001t0003g0274 a0001c0001t0003g0278 |
4 | HG02965.hp2 HG03098.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2481-253dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94178419 | |||||||
| chr1:94178498 | CATT | C | 56 | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0025 others(53): Show |
62 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.2481-334_2481-332d others(5): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94178498 | |||||||
| chr1:94178885 | T | G | 1 | a0001c0001t0013g0254 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2481-718A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94178885 | |||||||
| chr1:94179391 | C | T | 3 | a0001c0001t0007g0106 a0001c0001t0007g0109 a0001c0001t0007g0113 |
3 | HG02738.hp2 HG03491.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2480+334G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94179391 | |||||||
| chr1:94179492 | G | A | 1 | a0002c0003t0008g0296 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2480+233C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94179492 | |||||||
| chr1:94179549 | T | C | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2480+176A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94179549 | |||||||
| chr1:94179592 | C | CA | 12 | a0001c0001t0004g0053 a0001c0001t0004g0142 a0001c0001t0004g0143 others(9): Show |
12 | HG02145.hp1 HG02572.hp1 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.2480+132dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94179592 | |||||||
| chr1:94179592 | C | CAA | 29 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0023 others(26): Show |
35 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.2480+131_2480+132d others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94179592 | |||||||
| chr1:94179592 | C | CAAA | 8 | a0001c0001t0004g0022 a0001c0001t0004g0032 a0001c0001t0004g0050 others(5): Show |
9 | HG01928.hp1 HG02523.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.2480+130_2480+132d others(5): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94179592 | |||||||
| chr1:94179592 | CA | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(207): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.2480+132delT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94179592 | |||||||
| chr1:94179592 | CAA | C | 11 | a0001c0001t0002g0067 a0001c0001t0002g0304 a0001c0001t0003g0268 others(8): Show |
12 | HG01168.hp2 HG01891.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.2480+131_2480+132d others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | 94179592 | |||||||
| chr1:94180151 | GT | G | 8 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(5): Show |
9 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2248-195delA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180151 | |||||||
| chr1:94180243 | A | T | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2248-286T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180243 | |||||||
| chr1:94180320 | C | T | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2248-363G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180320 | |||||||
| chr1:94180421 | T | A | 1 | a0001c0001t0004g0210 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2248-464A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180421 | |||||||
| chr1:94180440 | A | G | 16 | a0001c0001t0005g0001 a0001c0001t0005g0005 a0001c0001t0005g0014 others(13): Show |
24 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2248-483T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180440 | |||||||
| chr1:94180496 | G | T | 1 | a0002c0003t0024g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2248-539C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180496 | |||||||
| chr1:94180572 | C | T | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2248-615G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180572 | |||||||
| chr1:94180711 | C | T | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2248-754G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180711 | |||||||
| chr1:94180790 | T | C | 39 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(36): Show |
46 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.2248-833A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180790 | |||||||
| chr1:94180883 | G | A | 37 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(34): Show |
44 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.2248-926C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180883 | |||||||
| chr1:94180958 | G | A | 33 | a0001c0001t0003g0006 a0001c0001t0003g0025 a0001c0001t0003g0026 others(30): Show |
37 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.2248-1001C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94180958 | |||||||
| chr1:94181047 | G | A | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2248-1090C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181047 | |||||||
| chr1:94181080 | C | T | 1 | a0001c0001t0007g0112 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2248-1123G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181080 | |||||||
| chr1:94181116 | A | G | 1 | a0001c0001t0037g0305 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2248-1159T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181116 | |||||||
| chr1:94181124 | A | C | 1 | a0001c0001t0038g0141 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2248-1167T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181124 | |||||||
| chr1:94181324 | C | G | 1 | a0001c0001t0001g0204 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2248-1367G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181324 | |||||||
| chr1:94181353 | C | T | 1 | a0001c0007t0001g0045 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2248-1396G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181353 | |||||||
| chr1:94181449 | T | C | 1 | a0001c0001t0004g0142 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2248-1492A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181449 | |||||||
| chr1:94181494 | G | A | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2248-1537C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181494 | |||||||
| chr1:94181603 | G | A | 10 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(7): Show |
11 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.2248-1646C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181603 | |||||||
| chr1:94181678 | A | T | 1 | a0001c0001t0003g0258 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2248-1721T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181678 | |||||||
| chr1:94181744 | AAAC | A | 3 | a0001c0001t0003g0026 a0001c0001t0003g0261 a0001c0001t0005g0117 |
4 | HG00280.hp1 HG02738.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.2248-1790_2248-178 others(7): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181744 | |||||||
| chr1:94181774 | T | C | 8 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(5): Show |
9 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2248-1817A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94181774 | |||||||
| chr1:94182100 | T | TA | 293 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(290): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.2247+2050dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182100 | |||||||
| chr1:94182129 | T | C | 2 | a0001c0001t0006g0103 a0001c0001t0006g0105 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2247+2022A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182129 | |||||||
| chr1:94182146 | G | A | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2247+2005C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182146 | |||||||
| chr1:94182239 | G | A | 8 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(5): Show |
9 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2247+1912C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182239 | |||||||
| chr1:94182273 | A | T | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2247+1878T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182273 | |||||||
| chr1:94182284 | A | G | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2247+1867T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182284 | |||||||
| chr1:94182315 | A | G | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2247+1836T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182315 | |||||||
| chr1:94182389 | A | T | 29 | a0001c0002t0001g0134 a0001c0002t0001g0135 a0001c0002t0001g0146 others(26): Show |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.2247+1762T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182389 | |||||||
| chr1:94182577 | A | G | 246 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(243): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.2247+1574T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182577 | |||||||
| chr1:94182580 | A | G | 302 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(299): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.2247+1571T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182580 | |||||||
| chr1:94182619 | A | C | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2247+1532T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182619 | |||||||
| chr1:94182736 | C | T | 1 | a0001c0001t0004g0206 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2247+1415G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182736 | |||||||
| chr1:94182811 | T | TAAAAC | 130 | a0001c0001t0001g0205 a0001c0001t0001g0233 a0001c0001t0002g0003 others(127): Show |
152 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.2247+1335_2247+133 others(9): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182811 | |||||||
| chr1:94182811 | T | TAAAACAA others(3): Show |
19 | a0001c0001t0001g0239 a0001c0001t0002g0043 a0001c0001t0002g0064 others(16): Show |
21 | HG00741.hp1 HG01884.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.2247+1330_2247+133 others(14): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182811 | |||||||
| chr1:94182811 | T | TAAAACAA others(8): Show |
1 | a0001c0001t0012g0264 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2247+1325_2247+133 others(19): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182811 | |||||||
| chr1:94182811 | T | TAAAACAA others(13): Show |
2 | a0001c0001t0018g0234 a0001c0001t0018g0235 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2247+1320_2247+133 others(24): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182811 | |||||||
| chr1:94182811 | TAAAAC | T | 6 | a0002c0003t0008g0293 a0002c0003t0015g0051 a0002c0003t0015g0052 others(3): Show |
6 | HG02723.hp1 HG02970.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2247+1335_2247+133 others(9): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182811 | |||||||
| chr1:94182811 | TAAAACAA others(3): Show |
T | 9 | a0001c0001t0001g0232 a0001c0001t0010g0016 a0001c0001t0010g0136 others(6): Show |
10 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.2247+1330_2247+133 others(14): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94182811 | |||||||
| chr1:94183138 | A | T | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2247+1013T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183138 | |||||||
| chr1:94183196 | TA | T | 107 | a0001c0001t0001g0233 a0001c0001t0002g0003 a0001c0001t0002g0011 others(104): Show |
124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.2247+954delT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183196 | |||||||
| chr1:94183204 | A | T | 9 | a0001c0001t0002g0042 a0001c0001t0002g0086 a0001c0001t0010g0016 others(6): Show |
10 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.2247+947T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183204 | |||||||
| chr1:94183204 | AT | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(134): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.2247+946delA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183204 | |||||||
| chr1:94183206 | T | A | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2247+945A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183206 | |||||||
| chr1:94183292 | T | C | 1 | a0001c0001t0004g0223 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2247+859A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183292 | |||||||
| chr1:94183357 | G | A | 1 | a0001c0001t0007g0104 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2247+794C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183357 | |||||||
| chr1:94183401 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0095 |
2 | HG04184.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.2247+750A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183401 | |||||||
| chr1:94183430 | T | C | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2247+721A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183430 | |||||||
| chr1:94183693 | C | T | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2247+458G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94183693 | |||||||
| chr1:94184036 | C | A | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2247+115G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94184036 | |||||||
| chr1:94184040 | T | C | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2247+111A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94184040 | |||||||
| chr1:94184044 | G | A | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2247+107C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94184044 | |||||||
| chr1:94184092 | CA | C | 7 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(4): Show |
8 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2247+58delT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | 94184092 | |||||||
| chr1:94184520 | A | C | 17 | a0001c0001t0005g0001 a0001c0001t0005g0005 a0001c0001t0005g0014 others(14): Show |
25 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.2110-232T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 18/22 | chr1 | 94184520 | |||||||
| chr1:94184556 | C | T | 2 | a0001c0001t0004g0032 a0001c0001t0036g0031 |
2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.2110-268G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 18/22 | chr1 | 94184556 | |||||||
| chr1:94184589 | A | T | 3 | a0001c0001t0004g0142 a0001c0001t0004g0143 a0002c0003t0008g0298 |
3 | HG02572.hp1 HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2109+283T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 18/22 | chr1 | 94184589 | |||||||
| chr1:94184590 | T | A | 10 | a0001c0001t0001g0200 a0001c0001t0007g0104 a0001c0001t0010g0016 others(7): Show |
11 | HG01109.hp1 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2109+282A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 18/22 | chr1 | 94184590 | |||||||
| chr1:94184624 | C | T | 1 | a0001c0001t0005g0123 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2109+248G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 18/22 | chr1 | 94184624 | |||||||
| chr1:94184838 | T | A | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2109+34A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 18/22 | chr1 | 94184838 | |||||||
| chr1:94184849 | A | C | 1 | a0008c0010t0022g0040 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2109+23T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 18/22 | chr1 | 94184849 | |||||||
| chr1:94185175 | T | C | 1 | a0002c0015t0024g0185 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1921-115A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 17/22 | chr1 | 94185175 | |||||||
| chr1:94185249 | T | C | 2 | a0001c0001t0004g0032 a0001c0001t0036g0031 |
2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1920+93A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 17/22 | chr1 | 94185249 | |||||||
| chr1:94185321 | A | C | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1920+21T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 17/22 | chr1 | 94185321 | |||||||
| chr1:94185676 | G | C | 8 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(5): Show |
9 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1781-195C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 16/22 | chr1 | 94185676 | |||||||
| chr1:94185690 | A | G | 1 | a0001c0001t0031g0118 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1781-209T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 16/22 | chr1 | 94185690 | |||||||
| chr1:94185795 | G | C | 1 | a0001c0001t0004g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1781-314C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 16/22 | chr1 | 94185795 | |||||||
| chr1:94185835 | A | G | 4 | a0002c0003t0015g0051 a0002c0003t0015g0052 a0002c0003t0015g0249 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1781-354T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 16/22 | chr1 | 94185835 | |||||||
| chr1:94186086 | C | T | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1780+413G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 16/22 | chr1 | 94186086 | |||||||
| chr1:94186091 | A | C | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1780+408T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 16/22 | chr1 | 94186091 | |||||||
| chr1:94186120 | T | C | 1 | a0001c0001t0037g0305 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1780+379A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 16/22 | chr1 | 94186120 | |||||||
| chr1:94186230 | T | C | 2 | a0001c0001t0022g0041 a0008c0010t0022g0040 |
2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1780+269A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 16/22 | chr1 | 94186230 | |||||||
| chr1:94186615 | A | C | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1682-18T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94186615 | |||||||
| chr1:94186955 | A | T | 31 | a0001c0001t0025g0247 a0001c0001t0025g0248 a0001c0002t0001g0134 others(28): Show |
31 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1682-358T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94186955 | |||||||
| chr1:94186972 | T | A | 2 | a0001c0001t0004g0032 a0001c0001t0036g0031 |
2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1682-375A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94186972 | |||||||
| chr1:94187027 | A | G | 2 | a0001c0001t0004g0032 a0001c0001t0036g0031 |
2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1682-430T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187027 | |||||||
| chr1:94187187 | C | T | 4 | a0002c0003t0015g0051 a0002c0003t0015g0052 a0002c0003t0015g0249 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1682-590G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187187 | |||||||
| chr1:94187250 | A | T | 2 | a0002c0003t0015g0249 a0002c0003t0015g0250 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1682-653T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187250 | |||||||
| chr1:94187279 | T | C | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1682-682A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187279 | |||||||
| chr1:94187291 | C | T | 2 | a0001c0001t0018g0234 a0001c0001t0018g0235 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1682-694G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187291 | |||||||
| chr1:94187376 | T | C | 2 | a0001c0001t0006g0082 a0001c0001t0006g0096 |
2 | NA19000.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1682-779A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187376 | |||||||
| chr1:94187382 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1682-785C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187382 | |||||||
| chr1:94187439 | G | A | 1 | a0001c0001t0005g0127 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1682-842C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187439 | |||||||
| chr1:94187444 | A | G | 8 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(5): Show |
9 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1682-847T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187444 | |||||||
| chr1:94187699 | A | T | 1 | a0001c0001t0001g0199 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1682-1102T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187699 | |||||||
| chr1:94187764 | G | A | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1681+1073C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187764 | |||||||
| chr1:94187806 | A | G | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1681+1031T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187806 | |||||||
| chr1:94187892 | T | A | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1681+945A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94187892 | |||||||
| chr1:94188126 | C | A | 2 | a0001c0001t0004g0142 a0001c0001t0004g0143 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1681+711G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94188126 | |||||||
| chr1:94188470 | A | G | 2 | a0001c0001t0022g0041 a0008c0010t0022g0040 |
2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1681+367T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94188470 | |||||||
| chr1:94188594 | G | A | 1 | a0001c0001t0036g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1681+243C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94188594 | |||||||
| chr1:94188602 | T | C | 1 | a0001c0001t0003g0261 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1681+235A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94188602 | |||||||
| chr1:94188669 | C | G | 301 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(298): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1681+168G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 15/22 | chr1 | 94188669 | |||||||
| chr1:94189025 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1577-84A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 14/22 | chr1 | 94189025 | |||||||
| chr1:94189510 | T | C | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1440-158A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 13/22 | chr1 | 94189510 | |||||||
| chr1:94189528 | T | G | 1 | a0001c0001t0038g0141 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1440-176A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 13/22 | chr1 | 94189528 | |||||||
| chr1:94189539 | G | A | 7 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(4): Show |
8 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1440-187C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 13/22 | chr1 | 94189539 | |||||||
| chr1:94189802 | T | C | 1 | a0001c0001t0002g0044 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1439+124A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 13/22 | chr1 | 94189802 | |||||||
| chr1:94190153 | T | G | 1 | a0001c0001t0004g0032 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1282-70A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94190153 | |||||||
| chr1:94190397 | C | A | 1 | a0001c0001t0004g0053 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1282-314G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94190397 | |||||||
| chr1:94190808 | C | T | 3 | a0001c0001t0042g0291 a0001c0001t0043g0290 a0001c0002t0016g0162 |
3 | HG01516.hp2 HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1282-725G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94190808 | |||||||
| chr1:94190811 | G | A | 4 | a0002c0003t0015g0051 a0002c0003t0015g0052 a0002c0003t0015g0249 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-728C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94190811 | |||||||
| chr1:94190816 | A | G | 1 | a0002c0003t0024g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1282-733T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94190816 | |||||||
| chr1:94190977 | A | G | 9 | a0001c0001t0002g0057 a0001c0001t0002g0061 a0001c0001t0002g0064 others(6): Show |
9 | HG00280.hp2 HG00642.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.1282-894T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94190977 | |||||||
| chr1:94191462 | T | C | 1 | a0001c0001t0037g0305 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1282-1379A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94191462 | |||||||
| chr1:94191492 | C | T | 7 | a0001c0001t0003g0027 a0001c0001t0003g0274 a0001c0001t0003g0275 others(4): Show |
8 | HG02109.hp1 HG02965.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.1282-1409G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94191492 | |||||||
| chr1:94191679 | G | C | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1282-1596C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94191679 | |||||||
| chr1:94192202 | C | T | 2 | a0001c0001t0004g0142 a0001c0001t0004g0143 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1282-2119G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94192202 | |||||||
| chr1:94192213 | G | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(135): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.1282-2130C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94192213 | |||||||
| chr1:94192297 | T | C | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1282-2214A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94192297 | |||||||
| chr1:94192422 | C | G | 41 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(38): Show |
48 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1282-2339G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94192422 | |||||||
| chr1:94192631 | A | T | 1 | a0001c0001t0007g0107 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1282-2548T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94192631 | |||||||
| chr1:94192738 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1282-2655G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94192738 | |||||||
| chr1:94192772 | A | G | 1 | a0001c0001t0004g0218 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1282-2689T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94192772 | |||||||
| chr1:94193013 | A | C | 300 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(297): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.1282-2930T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193013 | |||||||
| chr1:94193137 | G | A | 1 | a0001c0001t0017g0265 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1282-3054C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193137 | |||||||
| chr1:94193153 | A | C | 1 | a0001c0001t0001g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1282-3070T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193153 | |||||||
| chr1:94193185 | G | T | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1282-3102C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193185 | |||||||
| chr1:94193236 | A | T | 11 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0066 others(8): Show |
14 | HG00438.hp2 HG00558.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1282-3153T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193236 | |||||||
| chr1:94193302 | A | G | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1282-3219T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193302 | |||||||
| chr1:94193368 | C | CA | 10 | a0001c0001t0001g0171 a0001c0001t0002g0057 a0001c0001t0002g0092 others(7): Show |
10 | HG00280.hp2 HG01993.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1282-3286dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193368 | |||||||
| chr1:94193368 | CA | C | 77 | a0001c0001t0001g0054 a0001c0001t0001g0196 a0001c0001t0002g0260 others(74): Show |
92 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1282-3286delT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193368 | |||||||
| chr1:94193388 | A | T | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1282-3305T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193388 | |||||||
| chr1:94193415 | T | C | 57 | a0001c0001t0001g0054 a0001c0001t0002g0260 a0001c0001t0003g0006 others(54): Show |
63 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1282-3332A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193415 | |||||||
| chr1:94193493 | T | C | 1 | a0001c0001t0007g0112 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1282-3410A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193493 | |||||||
| chr1:94193677 | G | A | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1282-3594C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193677 | |||||||
| chr1:94193717 | C | T | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1282-3634G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193717 | |||||||
| chr1:94193772 | C | A | 1 | a0001c0001t0026g0128 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1282-3689G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193772 | |||||||
| chr1:94193803 | G | A | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1282-3720C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193803 | |||||||
| chr1:94193838 | C | G | 137 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(134): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1282-3755G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193838 | |||||||
| chr1:94193839 | T | C | 1 | a0001c0001t0003g0055 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1282-3756A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94193839 | |||||||
| chr1:94194327 | A | T | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1282-4244T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94194327 | |||||||
| chr1:94194404 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1282-4321A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94194404 | |||||||
| chr1:94194577 | CTT | C | 57 | a0001c0001t0001g0054 a0001c0001t0002g0260 a0001c0001t0003g0006 others(54): Show |
63 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.1282-4496_1282-449 others(6): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94194577 | |||||||
| chr1:94194770 | T | A | 302 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(299): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1282-4687A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94194770 | |||||||
| chr1:94194959 | CAAAAGTA | C | 39 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(36): Show |
46 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1282-4883_1282-487 others(11): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94194959 | |||||||
| chr1:94195006 | A | C | 4 | a0002c0003t0015g0051 a0002c0003t0015g0052 a0002c0003t0015g0249 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-4923T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195006 | |||||||
| chr1:94195053 | C | T | 41 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(38): Show |
48 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1282-4970G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195053 | |||||||
| chr1:94195123 | T | C | 1 | a0001c0002t0009g0160 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1282-5040A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195123 | |||||||
| chr1:94195126 | T | C | 1 | a0001c0001t0004g0053 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1282-5043A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195126 | |||||||
| chr1:94195215 | A | C | 2 | a0001c0001t0005g0122 a0001c0001t0005g0126 |
2 | NA18941.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1282-5132T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195215 | |||||||
| chr1:94195231 | T | C | 4 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0240 others(1): Show |
4 | HG00323.hp1 HG02683.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1282-5148A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195231 | |||||||
| chr1:94195246 | G | GA | 4 | a0001c0001t0001g0196 a0001c0001t0002g0092 a0001c0001t0004g0224 others(1): Show |
4 | HG01109.hp1 NA18961.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1282-5164dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195246 | |||||||
| chr1:94195273 | C | T | 1 | a0001c0001t0003g0281 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1282-5190G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195273 | |||||||
| chr1:94195299 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1282-5216A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195299 | |||||||
| chr1:94195322 | C | T | 16 | a0001c0001t0005g0001 a0001c0001t0005g0005 a0001c0001t0005g0014 others(13): Show |
24 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.1282-5239G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195322 | |||||||
| chr1:94195446 | T | C | 2 | a0001c0001t0025g0247 a0001c0001t0025g0248 |
2 | HG01243.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1282-5363A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195446 | |||||||
| chr1:94195588 | T | C | 29 | a0001c0002t0001g0134 a0001c0002t0001g0135 a0001c0002t0001g0146 others(26): Show |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.1282-5505A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195588 | |||||||
| chr1:94195594 | A | C | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1282-5511T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195594 | |||||||
| chr1:94195712 | T | C | 9 | a0001c0001t0004g0210 a0001c0001t0007g0110 a0001c0001t0010g0016 others(6): Show |
10 | HG01071.hp2 HG01891.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1282-5629A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195712 | |||||||
| chr1:94195720 | T | A | 8 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(5): Show |
9 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1282-5637A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195720 | |||||||
| chr1:94195920 | G | A | 1 | a0001c0001t0003g0261 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1281+5800C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94195920 | |||||||
| chr1:94196053 | C | A | 2 | a0001c0001t0018g0234 a0001c0001t0018g0235 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1281+5667G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196053 | |||||||
| chr1:94196061 | G | A | 107 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0012 others(104): Show |
124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1281+5659C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196061 | |||||||
| chr1:94196065 | A | T | 1 | a0001c0001t0017g0252 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1281+5655T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196065 | |||||||
| chr1:94196082 | T | A | 6 | a0001c0001t0002g0029 a0001c0001t0002g0308 a0001c0001t0002g0310 others(3): Show |
7 | HG01081.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1281+5638A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196082 | |||||||
| chr1:94196248 | G | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(186): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1281+5472C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196248 | |||||||
| chr1:94196249 | TG | T | 84 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0012 others(81): Show |
101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1281+5470delC | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196249 | |||||||
| chr1:94196250 | G | T | 21 | a0001c0001t0002g0039 a0001c0001t0002g0042 a0001c0001t0002g0044 others(18): Show |
21 | HG00621.hp2 HG01109.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.1281+5470C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196250 | |||||||
| chr1:94196254 | T | C | 19 | a0001c0001t0002g0039 a0001c0001t0002g0042 a0001c0001t0002g0044 others(16): Show |
19 | HG00621.hp2 HG01109.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1281+5466A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196254 | |||||||
| chr1:94196255 | T | C | 84 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0012 others(81): Show |
101 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1281+5465A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196255 | |||||||
| chr1:94196256 | C | CT | 71 | a0001c0001t0001g0054 a0001c0001t0002g0260 a0001c0001t0003g0006 others(68): Show |
77 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1281+5463dupA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196256 | |||||||
| chr1:94196256 | C | CTT | 15 | a0001c0001t0003g0046 a0001c0001t0003g0055 a0001c0001t0003g0178 others(12): Show |
15 | HG01192.hp1 HG01975.hp2 HG02148.hp1 others(12): Show |
intron_variant | MODIFIER | c.1281+5462_1281+546 others(6): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196256 | |||||||
| chr1:94196256 | C | T | 105 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0012 others(102): Show |
122 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1281+5464G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196256 | |||||||
| chr1:94196256 | CT | C | 11 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(8): Show |
12 | HG01891.hp2 HG02257.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1281+5463delA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196256 | |||||||
| chr1:94196259 | T | TC | 44 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(41): Show |
56 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1281+5460_1281+546 others(5): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196259 | |||||||
| chr1:94196260 | T | C | 3 | a0001c0001t0001g0169 a0001c0001t0001g0196 a0001c0001t0009g0203 |
3 | NA18961.hp2 NA18966.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.1281+5460A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196260 | |||||||
| chr1:94196262 | T | C | 1 | a0001c0001t0002g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1281+5458A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196262 | |||||||
| chr1:94196263 | T | TC | 38 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(35): Show |
45 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.1281+5456_1281+545 others(5): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196263 | |||||||
| chr1:94196264 | T | C | 1 | a0001c0001t0011g0214 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1281+5456A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196264 | |||||||
| chr1:94196293 | G | C | 1 | a0001c0001t0006g0251 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1281+5427C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196293 | |||||||
| chr1:94196348 | A | G | 1 | a0001c0001t0029g0056 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1281+5372T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196348 | |||||||
| chr1:94196386 | C | A | 2 | a0001c0001t0022g0041 a0008c0010t0022g0040 |
2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1281+5334G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196386 | |||||||
| chr1:94196422 | C | T | 9 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0050 others(6): Show |
13 | NA18941.hp2 NA18942.hp1 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.1281+5298G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196422 | |||||||
| chr1:94196451 | C | T | 1 | a0001c0001t0038g0141 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1281+5269G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196451 | |||||||
| chr1:94196507 | C | T | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1281+5213G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196507 | |||||||
| chr1:94196616 | T | C | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1281+5104A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196616 | |||||||
| chr1:94196867 | T | G | 1 | a0002c0015t0024g0185 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1281+4853A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196867 | |||||||
| chr1:94196916 | G | A | 1 | a0001c0001t0017g0266 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1281+4804C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94196916 | |||||||
| chr1:94197007 | T | C | 2 | a0001c0001t0003g0267 a0001c0001t0003g0268 |
2 | NA18962.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.1281+4713A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94197007 | |||||||
| chr1:94197071 | T | C | 2 | a0002c0003t0015g0249 a0002c0003t0015g0250 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1281+4649A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94197071 | |||||||
| chr1:94197113 | T | C | 1 | a0001c0001t0023g0179 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1281+4607A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94197113 | |||||||
| chr1:94197151 | T | C | 1 | a0001c0001t0003g0259 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1281+4569A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94197151 | |||||||
| chr1:94197168 | G | A | 1 | a0001c0001t0022g0041 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1281+4552C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94197168 | |||||||
| chr1:94197429 | C | T | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1281+4291G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94197429 | |||||||
| chr1:94197623 | T | C | 1 | a0001c0001t0004g0053 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1281+4097A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94197623 | |||||||
| chr1:94197884 | C | A | 1 | a0001c0001t0001g0196 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1281+3836G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94197884 | |||||||
| chr1:94197954 | C | T | 9 | a0001c0001t0004g0022 a0001c0001t0004g0210 a0001c0001t0004g0211 others(6): Show |
10 | HG02148.hp2 HG02280.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.1281+3766G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94197954 | |||||||
| chr1:94198184 | CAATT | C | 114 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0012 others(111): Show |
132 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1281+3532_1281+353 others(8): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198184 | |||||||
| chr1:94198409 | T | G | 1 | a0002c0015t0024g0185 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1281+3311A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198409 | |||||||
| chr1:94198564 | T | TA | 4 | a0001c0001t0011g0214 a0001c0001t0011g0216 a0001c0001t0032g0213 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1281+3155dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198564 | |||||||
| chr1:94198602 | G | A | 300 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(297): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.1281+3118C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198602 | |||||||
| chr1:94198704 | T | C | 1 | a0001c0001t0005g0124 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1281+3016A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198704 | |||||||
| chr1:94198732 | A | G | 4 | a0001c0002t0001g0156 a0001c0002t0001g0157 a0001c0002t0001g0240 others(1): Show |
4 | HG00323.hp1 HG02683.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1281+2988T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198732 | |||||||
| chr1:94198786 | A | G | 1 | a0001c0001t0003g0271 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1281+2934T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198786 | |||||||
| chr1:94198826 | G | A | 1 | a0001c0001t0036g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1281+2894C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198826 | |||||||
| chr1:94198857 | G | A | 4 | a0002c0003t0015g0051 a0002c0003t0015g0052 a0002c0003t0015g0249 others(1): Show |
4 | HG02723.hp1 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+2863C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198857 | |||||||
| chr1:94198964 | G | A | 301 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(298): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1281+2756C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198964 | |||||||
| chr1:94198994 | G | A | 1 | a0001c0001t0025g0248 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1281+2726C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94198994 | |||||||
| chr1:94199119 | A | G | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1281+2601T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199119 | |||||||
| chr1:94199213 | A | G | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1281+2507T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199213 | |||||||
| chr1:94199249 | A | G | 39 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(36): Show |
46 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1281+2471T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199249 | |||||||
| chr1:94199266 | G | A | 39 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(36): Show |
46 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1281+2454C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199266 | |||||||
| chr1:94199390 | AT | A | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1281+2329delA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199390 | |||||||
| chr1:94199460 | C | T | 2 | a0002c0003t0015g0249 a0002c0003t0015g0250 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1281+2260G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199460 | |||||||
| chr1:94199668 | ATGC | A | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1281+2049_1281+205 others(7): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199668 | |||||||
| chr1:94199693 | C | T | 296 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(293): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.1281+2027G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199693 | |||||||
| chr1:94199772 | C | T | 1 | a0001c0001t0006g0096 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1281+1948G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199772 | |||||||
| chr1:94199882 | T | C | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1281+1838A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199882 | |||||||
| chr1:94199907 | C | A | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1281+1813G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199907 | |||||||
| chr1:94199998 | C | T | 4 | a0001c0001t0002g0039 a0001c0001t0002g0067 a0001c0001t0002g0068 others(1): Show |
4 | HG01168.hp2 HG01192.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1281+1722G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94199998 | |||||||
| chr1:94200025 | T | C | 1 | a0001c0001t0004g0133 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1281+1695A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94200025 | |||||||
| chr1:94200279 | T | C | 3 | a0001c0001t0007g0236 a0001c0001t0019g0017 a0001c0001t0019g0182 |
4 | HG01257.hp1 HG01258.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1281+1441A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94200279 | |||||||
| chr1:94200312 | C | T | 2 | a0001c0001t0022g0041 a0008c0010t0022g0040 |
2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1281+1408G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94200312 | |||||||
| chr1:94200391 | C | T | 301 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(298): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
intron_variant | MODIFIER | c.1281+1329G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94200391 | |||||||
| chr1:94200392 | G | A | 2 | a0002c0003t0015g0249 a0002c0003t0015g0250 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1281+1328C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94200392 | |||||||
| chr1:94200587 | A | G | 2 | a0001c0001t0001g0020 a0001c0001t0001g0192 |
3 | HG00609.hp2 NA18953.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1281+1133T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94200587 | |||||||
| chr1:94200639 | G | A | 296 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(293): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.1281+1081C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94200639 | |||||||
| chr1:94201126 | CT | C | 37 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(34): Show |
44 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1281+593delA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201126 | |||||||
| chr1:94201348 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1281+372G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201348 | |||||||
| chr1:94201394 | T | C | 1 | a0002c0003t0008g0296 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1281+326A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201394 | |||||||
| chr1:94201401 | T | C | 1 | a0001c0001t0004g0206 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1281+319A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201401 | |||||||
| chr1:94201434 | T | C | 4 | a0001c0001t0001g0019 a0001c0001t0001g0198 a0001c0001t0009g0190 others(1): Show |
5 | HG00621.hp1 HG02040.hp1 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1281+286A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201434 | |||||||
| chr1:94201457 | C | G | 1 | a0002c0003t0024g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1281+263G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201457 | |||||||
| chr1:94201459 | TCCTTCCT others(5): Show |
T | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1281+249_1281+260d others(14): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201459 | |||||||
| chr1:94201477 | T | C | 2 | a0001c0001t0001g0049 a0001c0001t0003g0277 |
2 | HG02135.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1281+243A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201477 | |||||||
| chr1:94201506 | TTCTCTCT others(1): Show |
T | 3 | a0001c0001t0041g0116 a0001c0001t0042g0291 a0001c0001t0043g0290 |
3 | HG03471.hp2 HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1281+206_1281+213d others(10): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201506 | |||||||
| chr1:94201506 | TTCTCTCT others(5): Show |
T | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1281+202_1281+213d others(14): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201506 | |||||||
| chr1:94201506 | TTCTCTCT others(7): Show |
T | 286 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(283): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.1281+200_1281+213d others(16): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201506 | |||||||
| chr1:94201506 | TTCTCTCT others(9): Show |
T | 1 | a0001c0002t0001g0301 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1281+198_1281+213d others(18): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | 94201506 | |||||||
| chr1:94201874 | G | GA | 294 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(291): Show |
337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.1144-18dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 11/22 | chr1 | 94201874 | |||||||
| chr1:94201892 | G | C | 1 | a0001c0001t0002g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1144-35C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 11/22 | chr1 | 94201892 | |||||||
| chr1:94202067 | T | C | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1144-210A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 11/22 | chr1 | 94202067 | |||||||
| chr1:94202073 | A | G | 3 | a0001c0001t0006g0081 a0001c0001t0029g0056 a0003c0013t0006g0077 |
3 | HG00423.hp2 NA18965.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1144-216T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 11/22 | chr1 | 94202073 | |||||||
| chr1:94202366 | C | T | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1143+178G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 11/22 | chr1 | 94202366 | |||||||
| chr1:94202414 | T | C | 60 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0012 others(57): Show |
67 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1143+130A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 11/22 | chr1 | 94202414 | |||||||
| chr1:94202468 | C | T | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1143+76G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 11/22 | chr1 | 94202468 | |||||||
| chr1:94202490 | C | T | 288 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(285): Show |
330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.1143+54G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 11/22 | chr1 | 94202490 | |||||||
| chr1:94202810 | T | C | 2 | a0001c0001t0006g0091 a0001c0001t0006g0093 |
2 | NA18970.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.955-78A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 10/22 | chr1 | 94202810 | |||||||
| chr1:94203676 | A | C | 1 | a0001c0001t0017g0252 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.762+254T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 8/22 | chr1 | 94203676 | |||||||
| chr1:94203739 | C | T | 8 | a0001c0001t0002g0012 a0001c0001t0002g0085 a0001c0001t0002g0092 others(5): Show |
9 | HG02135.hp1 HG03831.hp2 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.762+191G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 8/22 | chr1 | 94203739 | |||||||
| chr1:94203751 | C | T | 42 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(39): Show |
49 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.762+179G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 8/22 | chr1 | 94203751 | |||||||
| chr1:94203826 | T | C | 1 | a0005c0014t0011g0215 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.762+104A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 8/22 | chr1 | 94203826 | |||||||
| chr1:94204144 | CT | C | 15 | a0001c0001t0002g0102 a0001c0001t0002g0292 a0001c0001t0004g0210 others(12): Show |
16 | HG01069.hp1 HG01891.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.698-151delA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204144 | |||||||
| chr1:94204160 | T | A | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.698-166A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204160 | |||||||
| chr1:94204161 | A | T | 19 | a0001c0001t0001g0047 a0001c0001t0001g0186 a0001c0001t0005g0001 others(16): Show |
27 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.698-167T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204161 | |||||||
| chr1:94204202 | G | C | 296 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(293): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.698-208C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204202 | |||||||
| chr1:94204305 | T | C | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.698-311A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204305 | |||||||
| chr1:94204535 | T | TTTAAGCA others(16): Show |
6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.697+503_697+525dup others(23): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204535 | |||||||
| chr1:94204678 | A | G | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.697+383T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204678 | |||||||
| chr1:94204722 | TTC | T | 41 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(38): Show |
48 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.697+337_697+338del others(2): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204722 | |||||||
| chr1:94204774 | T | C | 3 | a0001c0001t0018g0139 a0001c0001t0018g0234 a0001c0001t0018g0235 |
3 | HG02486.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.697+287A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204774 | |||||||
| chr1:94204842 | A | T | 1 | a0001c0001t0002g0064 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.697+219T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204842 | |||||||
| chr1:94204848 | T | C | 1 | a0002c0015t0024g0185 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.697+213A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 7/22 | chr1 | 94204848 | |||||||
| chr1:94205228 | T | C | 107 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0012 others(104): Show |
124 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.560-30A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 6/22 | chr1 | 94205228 | |||||||
| chr1:94205270 | G | A | 17 | a0001c0001t0005g0001 a0001c0001t0005g0005 a0001c0001t0005g0014 others(14): Show |
25 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.560-72C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 6/22 | chr1 | 94205270 | |||||||
| chr1:94205335 | T | C | 1 | a0001c0001t0028g0097 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.560-137A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 6/22 | chr1 | 94205335 | |||||||
| chr1:94205838 | A | G | 41 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(38): Show |
48 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.511-155T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94205838 | |||||||
| chr1:94205855 | T | C | 3 | a0001c0001t0003g0172 a0001c0001t0003g0175 a0001c0001t0003g0178 |
3 | HG01069.hp2 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.511-172A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94205855 | |||||||
| chr1:94205935 | A | G | 1 | a0001c0001t0035g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.511-252T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94205935 | |||||||
| chr1:94206213 | C | A | 1 | a0001c0001t0002g0061 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.511-530G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206213 | |||||||
| chr1:94206293 | G | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0169 a0001c0001t0001g0170 others(4): Show |
11 | HG02074.hp2 NA18747.hp2 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.511-610C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206293 | |||||||
| chr1:94206313 | G | A | 29 | a0001c0002t0001g0134 a0001c0002t0001g0135 a0001c0002t0001g0146 others(26): Show |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.511-630C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206313 | |||||||
| chr1:94206347 | T | C | 1 | a0001c0001t0005g0125 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.511-664A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206347 | |||||||
| chr1:94206641 | A | C | 1 | a0001c0001t0004g0217 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.511-958T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206641 | |||||||
| chr1:94206645 | A | C | 296 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(293): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.511-962T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206645 | |||||||
| chr1:94206861 | A | ACT | 296 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(293): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.511-1179_511-1178i others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206861 | |||||||
| chr1:94206909 | T | A | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.511-1226A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206909 | |||||||
| chr1:94206925 | T | C | 1 | a0001c0001t0001g0239 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.511-1242A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206925 | |||||||
| chr1:94206966 | A | AAT | 4 | a0001c0002t0016g0145 a0001c0002t0016g0162 a0001c0002t0016g0163 others(1): Show |
4 | HG00140.hp1 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-1285_511-1284d others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206966 | |||||||
| chr1:94206976 | T | G | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.511-1293A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206976 | |||||||
| chr1:94206978 | T | G | 69 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0018 others(66): Show |
82 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.511-1295A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206978 | |||||||
| chr1:94206980 | G | T | 49 | a0001c0001t0001g0115 a0001c0001t0002g0084 a0001c0001t0002g0114 others(46): Show |
50 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.511-1297C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206980 | |||||||
| chr1:94206982 | G | T | 1 | a0001c0002t0001g0146 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.511-1299C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94206982 | |||||||
| chr1:94207001 | T | TTTTA | 16 | a0001c0001t0004g0022 a0001c0001t0004g0032 a0001c0001t0004g0053 others(13): Show |
17 | HG02145.hp1 HG02148.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.511-1322_511-1319d others(6): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207001 | |||||||
| chr1:94207001 | T | TTTTATTT others(1): Show |
23 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0023 others(20): Show |
28 | HG00558.hp2 HG00597.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.511-1326_511-1319d others(10): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207001 | |||||||
| chr1:94207001 | T | TTTTATTT others(5): Show |
2 | a0001c0001t0004g0206 a0001c0001t0014g0024 |
3 | HG00323.hp2 HG01074.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.511-1330_511-1319d others(14): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207001 | |||||||
| chr1:94207066 | C | T | 2 | a0001c0001t0005g0014 a0001c0001t0005g0120 |
3 | HG02056.hp2 HG02129.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.511-1383G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207066 | |||||||
| chr1:94207113 | A | AT | 288 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(285): Show |
330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.511-1431dupA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207113 | |||||||
| chr1:94207119 | G | A | 60 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0012 others(57): Show |
67 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.511-1436C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207119 | |||||||
| chr1:94207260 | C | T | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.510+1572G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207260 | |||||||
| chr1:94207301 | C | T | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.510+1531G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207301 | |||||||
| chr1:94207389 | C | T | 1 | a0001c0001t0014g0306 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.510+1443G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207389 | |||||||
| chr1:94207550 | CCA | C | 288 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(285): Show |
330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.510+1280_510+1281d others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207550 | |||||||
| chr1:94207581 | T | C | 1 | a0001c0007t0001g0045 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.510+1251A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207581 | |||||||
| chr1:94207622 | T | G | 1 | a0001c0001t0002g0302 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.510+1210A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207622 | |||||||
| chr1:94207631 | G | A | 41 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(38): Show |
48 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.510+1201C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207631 | |||||||
| chr1:94207787 | G | A | 296 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(293): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.510+1045C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207787 | |||||||
| chr1:94207838 | T | G | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.510+994A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207838 | |||||||
| chr1:94207841 | T | G | 1 | a0001c0001t0004g0208 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.510+991A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207841 | |||||||
| chr1:94207844 | G | T | 2 | a0001c0001t0005g0001 a0001c0001t0005g0123 |
3 | NA18971.hp2 NA18986.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.510+988C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207844 | |||||||
| chr1:94207871 | G | A | 1 | a0002c0003t0015g0051 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.510+961C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207871 | |||||||
| chr1:94207879 | C | T | 1 | a0001c0001t0035g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.510+953G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207879 | |||||||
| chr1:94207895 | G | A | 1 | a0001c0001t0007g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.510+937C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94207895 | |||||||
| chr1:94208071 | C | G | 1 | a0002c0003t0008g0299 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.510+761G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94208071 | |||||||
| chr1:94208382 | T | A | 1 | a0001c0001t0026g0128 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.510+450A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94208382 | |||||||
| chr1:94208639 | T | C | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.510+193A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94208639 | |||||||
| chr1:94208656 | C | A | 2 | a0001c0001t0004g0142 a0001c0001t0004g0143 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.510+176G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | 94208656 | |||||||
| chr1:94209000 | T | C | 1 | a0001c0001t0010g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.438-96A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 4/22 | chr1 | 94209000 | |||||||
| chr1:94209167 | G | A | 302 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(299): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.437+87C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 4/22 | chr1 | 94209167 | |||||||
| chr1:94209170 | T | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(54): Show |
71 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.437+84A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 4/22 | chr1 | 94209170 | |||||||
| chr1:94209524 | C | T | 5 | a0001c0001t0001g0019 a0001c0001t0001g0189 a0001c0001t0001g0198 others(2): Show |
6 | HG00621.hp1 HG02040.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.341-174G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94209524 | |||||||
| chr1:94209711 | G | A | 1 | a0001c0002t0009g0154 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.341-361C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94209711 | |||||||
| chr1:94209764 | T | C | 1 | a0001c0001t0002g0074 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.341-414A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94209764 | |||||||
| chr1:94209812 | TATATAC | T | 288 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(285): Show |
330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.341-468_341-463del others(6): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94209812 | |||||||
| chr1:94210149 | T | C | 2 | a0001c0001t0022g0041 a0008c0010t0022g0040 |
2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.341-799A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210149 | |||||||
| chr1:94210163 | C | T | 1 | a0001c0001t0036g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.341-813G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210163 | |||||||
| chr1:94210237 | G | A | 1 | a0001c0001t0007g0108 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.341-887C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210237 | |||||||
| chr1:94210243 | T | G | 296 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(293): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.341-893A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210243 | |||||||
| chr1:94210259 | G | C | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.341-909C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210259 | |||||||
| chr1:94210395 | T | C | 1 | a0001c0001t0011g0226 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.341-1045A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210395 | |||||||
| chr1:94210445 | G | C | 1 | a0001c0001t0004g0225 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.341-1095C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210445 | |||||||
| chr1:94210602 | C | G | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.341-1252G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210602 | |||||||
| chr1:94210606 | CAAAAAG | C | 4 | a0001c0002t0016g0145 a0001c0002t0016g0162 a0001c0002t0016g0163 others(1): Show |
4 | HG00140.hp1 HG01123.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.341-1262_341-1257d others(8): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210606 | |||||||
| chr1:94210712 | T | G | 40 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(37): Show |
47 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.341-1362A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210712 | |||||||
| chr1:94210787 | C | T | 1 | a0001c0002t0001g0134 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.341-1437G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210787 | |||||||
| chr1:94210802 | G | C | 296 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(293): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.341-1452C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210802 | |||||||
| chr1:94210904 | TA | T | 281 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(278): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.341-1555delT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210904 | |||||||
| chr1:94210904 | TAA | T | 7 | a0001c0001t0004g0209 a0001c0001t0004g0210 a0001c0001t0007g0035 others(4): Show |
7 | HG02895.hp2 HG03471.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.341-1556_341-1555d others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210904 | |||||||
| chr1:94210943 | C | A | 1 | a0001c0001t0035g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.341-1593G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210943 | |||||||
| chr1:94210948 | G | T | 1 | a0001c0001t0001g0188 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.341-1598C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94210948 | |||||||
| chr1:94211093 | T | C | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.341-1743A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211093 | |||||||
| chr1:94211287 | C | CA | 8 | a0001c0001t0001g0242 a0001c0001t0003g0172 a0001c0001t0018g0234 others(5): Show |
8 | HG00438.hp2 HG01069.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.341-1938dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | |||||||
| chr1:94211287 | C | CAA | 34 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(31): Show |
46 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.341-1939_341-1938d others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | |||||||
| chr1:94211287 | C | CAAA | 33 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0049 others(30): Show |
35 | HG00621.hp1 HG00733.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.341-1940_341-1938d others(5): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | |||||||
| chr1:94211287 | C | CAAAA | 72 | a0001c0001t0001g0233 a0001c0001t0002g0003 a0001c0001t0002g0011 others(69): Show |
83 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.341-1941_341-1938d others(6): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | |||||||
| chr1:94211287 | C | CAAAAA | 37 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0029 others(34): Show |
42 | HG00408.hp1 HG00423.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.341-1942_341-1938d others(7): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | |||||||
| chr1:94211287 | C | CAAAAAA | 9 | a0001c0001t0002g0094 a0001c0001t0002g0231 a0001c0001t0007g0037 others(6): Show |
10 | HG00735.hp2 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.341-1943_341-1938d others(8): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | |||||||
| chr1:94211287 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0006g0096 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.341-1949_341-1938d others(14): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | |||||||
| chr1:94211287 | C | CCA | 4 | a0001c0001t0010g0016 a0001c0001t0010g0138 a0001c0001t0010g0238 others(1): Show |
5 | HG01891.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.341-1938_341-1937i others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | |||||||
| chr1:94211287 | CAA | C | 9 | a0001c0001t0003g0055 a0001c0001t0003g0132 a0001c0001t0003g0257 others(6): Show |
9 | HG01358.hp1 HG02027.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-1939_341-1938d others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | |||||||
| chr1:94211287 | CAAA | C | 36 | a0001c0001t0001g0054 a0001c0001t0002g0260 a0001c0001t0003g0009 others(33): Show |
40 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.341-1940_341-1938d others(5): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | |||||||
| chr1:94211287 | CAAAAAAA others(4): Show |
C | 1 | a0009c0006t0001g0187 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.341-1948_341-1938d others(13): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | |||||||
| chr1:94211287 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0002g0080 a0001c0001t0002g0102 |
2 | HG00609.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.341-1949_341-1938d others(14): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211287 | |||||||
| chr1:94211299 | A | AAAAAC | 35 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(32): Show |
42 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.341-1950_341-1949i others(7): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211299 | |||||||
| chr1:94211305 | A | C | 40 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(37): Show |
47 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.341-1955T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211305 | |||||||
| chr1:94211319 | T | C | 138 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(135): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.341-1969A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211319 | |||||||
| chr1:94211387 | C | T | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-2037G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211387 | |||||||
| chr1:94211599 | T | C | 1 | a0001c0001t0003g0270 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.341-2249A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211599 | |||||||
| chr1:94211641 | T | C | 1 | a0001c0001t0002g0076 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.341-2291A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211641 | |||||||
| chr1:94211745 | T | A | 288 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(285): Show |
330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.341-2395A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211745 | |||||||
| chr1:94211911 | A | C | 296 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(293): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.341-2561T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211911 | |||||||
| chr1:94211936 | G | C | 288 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(285): Show |
330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.341-2586C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94211936 | |||||||
| chr1:94212142 | G | A | 296 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(293): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.341-2792C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212142 | |||||||
| chr1:94212176 | A | G | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-2826T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212176 | |||||||
| chr1:94212212 | C | G | 1 | a0001c0001t0004g0209 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.341-2862G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212212 | |||||||
| chr1:94212419 | C | T | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.341-3069G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212419 | |||||||
| chr1:94212538 | T | C | 1 | a0002c0015t0024g0185 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.341-3188A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212538 | |||||||
| chr1:94212562 | G | A | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.341-3212C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212562 | |||||||
| chr1:94212587 | T | C | 1 | a0001c0001t0003g0278 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.341-3237A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212587 | |||||||
| chr1:94212669 | C | T | 296 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(293): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.341-3319G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212669 | |||||||
| chr1:94212726 | T | C | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-3376A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212726 | |||||||
| chr1:94212956 | T | C | 88 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0012 others(85): Show |
97 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.341-3606A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94212956 | |||||||
| chr1:94213038 | C | T | 1 | a0001c0001t0004g0208 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.341-3688G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94213038 | |||||||
| chr1:94213081 | G | A | 2 | a0001c0001t0002g0072 a0001c0001t0002g0099 |
2 | NA18967.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.341-3731C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94213081 | |||||||
| chr1:94213192 | T | C | 1 | a0001c0001t0004g0227 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.341-3842A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94213192 | |||||||
| chr1:94213242 | T | C | 2 | a0002c0003t0015g0051 a0002c0003t0015g0052 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.341-3892A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94213242 | |||||||
| chr1:94213338 | C | T | 1 | a0001c0001t0037g0305 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.341-3988G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94213338 | |||||||
| chr1:94213364 | A | G | 2 | a0001c0001t0004g0032 a0001c0001t0036g0031 |
2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.341-4014T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94213364 | |||||||
| chr1:94213455 | T | C | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.341-4105A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94213455 | |||||||
| chr1:94213542 | G | A | 296 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(293): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.341-4192C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94213542 | |||||||
| chr1:94213633 | T | A | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.341-4283A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94213633 | |||||||
| chr1:94214007 | T | G | 2 | a0001c0001t0004g0032 a0001c0001t0036g0031 |
2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.341-4657A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214007 | |||||||
| chr1:94214042 | G | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(54): Show |
71 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.341-4692C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214042 | |||||||
| chr1:94214083 | A | G | 296 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(293): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.341-4733T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214083 | |||||||
| chr1:94214099 | G | A | 1 | a0002c0003t0024g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.341-4749C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214099 | |||||||
| chr1:94214179 | T | C | 1 | a0001c0001t0023g0179 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.341-4829A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214179 | |||||||
| chr1:94214292 | G | A | 7 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(4): Show |
8 | HG00639.hp2 HG01891.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.341-4942C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214292 | |||||||
| chr1:94214587 | T | G | 1 | a0002c0015t0024g0185 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.341-5237A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214587 | |||||||
| chr1:94214629 | A | G | 29 | a0001c0002t0001g0134 a0001c0002t0001g0135 a0001c0002t0001g0146 others(26): Show |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.341-5279T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214629 | |||||||
| chr1:94214719 | T | C | 296 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(293): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.341-5369A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214719 | |||||||
| chr1:94214753 | A | C | 1 | a0001c0001t0002g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.341-5403T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214753 | |||||||
| chr1:94214765 | C | T | 2 | a0001c0001t0007g0236 a0001c0001t0036g0031 |
2 | HG02145.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.341-5415G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214765 | |||||||
| chr1:94214773 | A | T | 1 | a0001c0001t0004g0133 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.341-5423T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94214773 | |||||||
| chr1:94215104 | G | GA | 63 | a0001c0001t0001g0204 a0001c0001t0004g0004 a0001c0001t0004g0010 others(60): Show |
72 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.340+5153dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94215104 | |||||||
| chr1:94215104 | GA | G | 10 | a0001c0001t0001g0054 a0001c0001t0002g0260 a0001c0001t0003g0009 others(7): Show |
11 | HG01258.hp1 HG01981.hp1 HG04204.hp1 others(8): Show |
intron_variant | MODIFIER | c.340+5153delT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94215104 | |||||||
| chr1:94215135 | C | T | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.340+5123G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94215135 | |||||||
| chr1:94215329 | A | C | 1 | a0002c0015t0024g0185 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.340+4929T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94215329 | |||||||
| chr1:94215544 | AG | A | 17 | a0001c0001t0005g0001 a0001c0001t0005g0005 a0001c0001t0005g0014 others(14): Show |
25 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.340+4713delC | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94215544 | |||||||
| chr1:94215938 | C | CAAATG | 300 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(297): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.340+4319_340+4320i others(7): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94215938 | |||||||
| chr1:94216210 | T | C | 49 | a0001c0001t0001g0054 a0001c0001t0002g0260 a0001c0001t0003g0009 others(46): Show |
53 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.340+4048A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94216210 | |||||||
| chr1:94216247 | T | G | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.340+4011A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94216247 | |||||||
| chr1:94216378 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.340+3880G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94216378 | |||||||
| chr1:94216392 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0047 a0001c0001t0001g0186 |
4 | NA18968.hp2 NA18974.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+3866G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94216392 | |||||||
| chr1:94216438 | T | C | 1 | a0001c0001t0041g0116 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.340+3820A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94216438 | |||||||
| chr1:94217367 | C | T | 1 | a0001c0001t0004g0207 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.340+2891G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217367 | |||||||
| chr1:94217471 | C | T | 1 | a0001c0001t0037g0305 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.340+2787G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217471 | |||||||
| chr1:94217508 | G | A | 1 | a0001c0001t0018g0139 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.340+2750C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217508 | |||||||
| chr1:94217508 | G | T | 300 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(297): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.340+2750C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217508 | |||||||
| chr1:94217529 | C | CA | 6 | a0001c0001t0004g0228 a0001c0001t0004g0230 a0001c0001t0011g0229 others(3): Show |
6 | HG00597.hp1 HG02970.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.340+2728dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217529 | |||||||
| chr1:94217529 | CA | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(230): Show |
268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.340+2728delT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217529 | |||||||
| chr1:94217547 | C | A | 1 | a0001c0001t0018g0139 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.340+2711G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217547 | |||||||
| chr1:94217549 | C | T | 1 | a0001c0001t0018g0139 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.340+2709G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217549 | |||||||
| chr1:94217746 | C | T | 1 | a0001c0001t0005g0119 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.340+2512G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217746 | |||||||
| chr1:94217779 | T | G | 1 | a0002c0015t0024g0185 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.340+2479A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217779 | |||||||
| chr1:94217842 | C | T | 5 | a0001c0002t0001g0146 a0001c0002t0001g0147 a0001c0002t0001g0148 others(2): Show |
5 | HG01433.hp2 HG01496.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+2416G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217842 | |||||||
| chr1:94217860 | CA | C | 9 | a0001c0001t0002g0098 a0001c0001t0003g0079 a0001c0001t0004g0143 others(6): Show |
9 | HG02572.hp1 HG02723.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.340+2397delT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217860 | |||||||
| chr1:94217860 | CAA | C | 292 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(289): Show |
335 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.340+2396_340+2397d others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217860 | |||||||
| chr1:94217862 | A | C | 1 | a0001c0001t0010g0136 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.340+2396T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217862 | |||||||
| chr1:94217871 | A | C | 50 | a0001c0001t0001g0054 a0001c0001t0002g0260 a0001c0001t0003g0009 others(47): Show |
54 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.340+2387T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217871 | |||||||
| chr1:94217872 | A | C | 288 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(285): Show |
330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.340+2386T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94217872 | |||||||
| chr1:94218199 | A | G | 49 | a0001c0001t0001g0054 a0001c0001t0002g0260 a0001c0001t0003g0009 others(46): Show |
53 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.340+2059T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94218199 | |||||||
| chr1:94218262 | T | C | 287 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(284): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.340+1996A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94218262 | |||||||
| chr1:94218495 | C | G | 1 | a0001c0001t0002g0078 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.340+1763G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94218495 | |||||||
| chr1:94218562 | A | G | 1 | a0001c0001t0003g0168 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.340+1696T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94218562 | |||||||
| chr1:94218581 | T | A | 4 | a0001c0001t0002g0039 a0001c0001t0002g0067 a0001c0001t0002g0068 others(1): Show |
4 | HG01168.hp2 HG01192.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+1677A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94218581 | |||||||
| chr1:94218763 | A | T | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.340+1495T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94218763 | |||||||
| chr1:94218784 | G | A | 1 | a0001c0001t0026g0128 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.340+1474C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94218784 | |||||||
| chr1:94218849 | T | C | 1 | a0001c0001t0002g0101 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.340+1409A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94218849 | |||||||
| chr1:94218950 | G | T | 1 | a0002c0015t0024g0185 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.340+1308C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94218950 | |||||||
| chr1:94219011 | C | G | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+1247G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219011 | |||||||
| chr1:94219056 | T | C | 1 | a0001c0001t0035g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.340+1202A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219056 | |||||||
| chr1:94219136 | C | T | 2 | a0001c0001t0002g0308 a0001c0001t0007g0307 |
2 | HG02630.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.340+1122G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219136 | |||||||
| chr1:94219259 | A | ACCCTGCA others(10): Show |
293 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(290): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.340+998_340+999ins others(17): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219259 | |||||||
| chr1:94219440 | C | T | 1 | a0003c0013t0006g0077 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.340+818G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219440 | |||||||
| chr1:94219631 | C | G | 1 | a0001c0001t0004g0206 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.340+627G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219631 | |||||||
| chr1:94219791 | A | G | 1 | a0001c0001t0036g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.340+467T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219791 | |||||||
| chr1:94219806 | A | C | 1 | a0001c0002t0016g0145 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.340+452T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219806 | |||||||
| chr1:94219918 | T | C | 293 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(290): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.340+340A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219918 | |||||||
| chr1:94219919 | T | A | 302 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(299): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.340+339A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219919 | |||||||
| chr1:94219966 | C | A | 1 | a0001c0012t0007g0184 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.340+292G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94219966 | |||||||
| chr1:94220029 | T | G | 46 | a0001c0001t0004g0004 a0001c0001t0004g0010 a0001c0001t0004g0022 others(43): Show |
53 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.340+229A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94220029 | |||||||
| chr1:94220039 | T | A | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.340+219A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | 94220039 | |||||||
| chr1:94220487 | T | C | 1 | a0001c0001t0002g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.206-95A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94220487 | |||||||
| chr1:94220554 | A | T | 110 | a0001c0001t0001g0066 a0001c0001t0001g0095 a0001c0001t0002g0003 others(107): Show |
127 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.206-162T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94220554 | |||||||
| chr1:94220570 | A | G | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.206-178T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94220570 | |||||||
| chr1:94220735 | A | AT | 51 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0287 others(48): Show |
57 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.206-344dupA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94220735 | |||||||
| chr1:94220871 | G | GA | 29 | a0001c0002t0001g0134 a0001c0002t0001g0135 a0001c0002t0001g0146 others(26): Show |
29 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.206-480dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94220871 | |||||||
| chr1:94220984 | A | G | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.206-592T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94220984 | |||||||
| chr1:94221021 | A | G | 1 | a0001c0001t0020g0312 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.206-629T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94221021 | |||||||
| chr1:94221059 | C | G | 6 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.206-667G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94221059 | |||||||
| chr1:94221093 | C | T | 1 | a0001c0011t0040g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.206-701G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94221093 | |||||||
| chr1:94221111 | C | T | 8 | a0001c0001t0002g0042 a0001c0001t0002g0044 a0001c0001t0002g0073 others(5): Show |
8 | NA18947.hp1 NA18949.hp2 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.206-719G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94221111 | |||||||
| chr1:94221357 | GGTGTTTA others(3): Show |
G | 1 | a0001c0001t0005g0117 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.206-975_206-966del others(10): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94221357 | |||||||
| chr1:94221524 | A | G | 1 | a0002c0003t0024g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.206-1132T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94221524 | |||||||
| chr1:94221565 | A | AT | 256 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(253): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.206-1174dupA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94221565 | |||||||
| chr1:94221919 | A | C | 1 | a0001c0001t0005g0119 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.206-1527T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94221919 | |||||||
| chr1:94221974 | T | TA | 94 | a0001c0001t0001g0054 a0001c0001t0001g0066 a0001c0001t0001g0095 others(91): Show |
104 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.206-1583dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94221974 | |||||||
| chr1:94222018 | A | C | 7 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(4): Show |
8 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.206-1626T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222018 | |||||||
| chr1:94222056 | G | A | 1 | a0001c0001t0003g0046 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.206-1664C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222056 | |||||||
| chr1:94222119 | A | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(124): Show |
146 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.206-1727T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222119 | |||||||
| chr1:94222206 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.206-1814A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222206 | |||||||
| chr1:94222280 | T | C | 1 | a0001c0001t0002g0043 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.206-1888A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222280 | |||||||
| chr1:94222391 | G | C | 1 | a0001c0001t0028g0097 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.206-1999C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222391 | |||||||
| chr1:94222404 | T | A | 1 | a0001c0001t0037g0305 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.206-2012A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222404 | |||||||
| chr1:94222445 | G | A | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.206-2053C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222445 | |||||||
| chr1:94222495 | T | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(255): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.206-2103A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222495 | |||||||
| chr1:94222705 | G | A | 2 | a0002c0003t0015g0249 a0002c0003t0015g0250 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.206-2313C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222705 | |||||||
| chr1:94222784 | T | TAATACAG others(6052): Show |
1 | a0001c0001t0001g0233 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.206-2393_206-2392i others(6061): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222784 | |||||||
| chr1:94222849 | C | A | 302 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(299): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.206-2457G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222849 | |||||||
| chr1:94222948 | A | AT | 235 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(232): Show |
264 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.206-2557dupA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222948 | |||||||
| chr1:94222948 | A | ATT | 22 | a0001c0001t0001g0129 a0001c0001t0003g0033 a0001c0001t0003g0131 others(19): Show |
30 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.206-2558_206-2557d others(4): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94222948 | |||||||
| chr1:94223045 | G | A | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.206-2653C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223045 | |||||||
| chr1:94223075 | T | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(255): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.206-2683A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223075 | |||||||
| chr1:94223088 | C | T | 6 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(3): Show |
6 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.206-2696G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223088 | |||||||
| chr1:94223172 | C | T | 1 | a0001c0001t0036g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.206-2780G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223172 | |||||||
| chr1:94223235 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.206-2843G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223235 | |||||||
| chr1:94223414 | T | C | 1 | a0001c0001t0005g0130 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.206-3022A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223414 | |||||||
| chr1:94223465 | G | A | 7 | a0001c0001t0003g0027 a0001c0001t0003g0274 a0001c0001t0003g0275 others(4): Show |
8 | HG02109.hp1 HG02965.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.206-3073C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223465 | |||||||
| chr1:94223471 | A | G | 256 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(253): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.206-3079T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223471 | |||||||
| chr1:94223502 | G | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(249): Show |
289 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.206-3110C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223502 | |||||||
| chr1:94223550 | G | T | 1 | a0001c0001t0025g0247 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.206-3158C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223550 | |||||||
| chr1:94223584 | A | G | 7 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(4): Show |
8 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.206-3192T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223584 | |||||||
| chr1:94223733 | G | T | 1 | a0001c0001t0006g0070 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.206-3341C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223733 | |||||||
| chr1:94223808 | C | T | 258 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(255): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.206-3416G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223808 | |||||||
| chr1:94223820 | C | T | 1 | a0001c0001t0002g0044 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.206-3428G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223820 | |||||||
| chr1:94223821 | T | C | 1 | a0001c0001t0002g0044 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.206-3429A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223821 | |||||||
| chr1:94223847 | G | A | 2 | a0001c0001t0018g0234 a0001c0001t0018g0235 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.206-3455C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223847 | |||||||
| chr1:94223872 | A | G | 1 | a0001c0001t0002g0069 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.206-3480T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94223872 | |||||||
| chr1:94224032 | C | T | 4 | a0001c0001t0002g0039 a0001c0001t0002g0067 a0001c0001t0002g0068 others(1): Show |
4 | HG01168.hp2 HG01192.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.206-3640G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224032 | |||||||
| chr1:94224088 | C | A | 31 | a0001c0001t0003g0006 a0001c0001t0003g0033 a0001c0002t0001g0134 others(28): Show |
33 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.206-3696G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224088 | |||||||
| chr1:94224151 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.206-3759G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224151 | |||||||
| chr1:94224178 | A | G | 11 | a0001c0001t0001g0007 a0001c0001t0001g0174 a0001c0001t0001g0176 others(8): Show |
13 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.206-3786T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224178 | |||||||
| chr1:94224388 | G | T | 9 | a0001c0001t0002g0057 a0001c0001t0002g0061 a0001c0001t0002g0064 others(6): Show |
9 | HG00280.hp2 HG00642.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.206-3996C>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224388 | |||||||
| chr1:94224432 | A | G | 1 | a0001c0001t0035g0140 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.206-4040T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224432 | |||||||
| chr1:94224631 | A | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(255): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.206-4239T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224631 | |||||||
| chr1:94224715 | T | C | 1 | a0002c0003t0008g0294 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.206-4323A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224715 | |||||||
| chr1:94224885 | T | C | 2 | a0001c0001t0003g0131 a0001c0001t0003g0132 |
2 | NA18963.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.206-4493A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224885 | |||||||
| chr1:94224905 | T | C | 1 | a0001c0001t0003g0279 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.206-4513A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224905 | |||||||
| chr1:94224908 | G | A | 2 | a0001c0002t0001g0166 a0001c0002t0001g0167 |
2 | HG01358.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.206-4516C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94224908 | |||||||
| chr1:94225175 | A | T | 8 | a0001c0001t0003g0257 a0001c0001t0013g0254 a0001c0001t0013g0256 others(5): Show |
9 | HG00544.hp1 HG00597.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.206-4783T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94225175 | |||||||
| chr1:94225239 | T | C | 252 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(249): Show |
289 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.206-4847A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94225239 | |||||||
| chr1:94225306 | A | C | 1 | a0001c0001t0031g0118 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.206-4914T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94225306 | |||||||
| chr1:94225418 | C | T | 302 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(299): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.206-5026G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94225418 | |||||||
| chr1:94225473 | A | T | 7 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(4): Show |
8 | HG01891.hp2 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.206-5081T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94225473 | |||||||
| chr1:94225522 | C | T | 95 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(92): Show |
112 | HG00140.hp2 HG00323.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.206-5130G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94225522 | |||||||
| chr1:94225543 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0169 a0001c0001t0001g0170 others(2): Show |
9 | NA18952.hp1 NA18970.hp1 NA18973.hp2 others(6): Show |
intron_variant | MODIFIER | c.206-5151T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94225543 | |||||||
| chr1:94225684 | T | C | 127 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(124): Show |
146 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.206-5292A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94225684 | |||||||
| chr1:94225995 | T | C | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.205+5412A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94225995 | |||||||
| chr1:94226106 | A | C | 255 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(252): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(289): Show |
intron_variant | MODIFIER | c.205+5301T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94226106 | |||||||
| chr1:94226357 | T | A | 1 | a0001c0001t0002g0098 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.205+5050A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94226357 | |||||||
| chr1:94226388 | T | A | 1 | a0001c0001t0002g0099 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.205+5019A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94226388 | |||||||
| chr1:94226583 | T | A | 31 | a0001c0001t0003g0006 a0001c0001t0003g0033 a0001c0002t0001g0134 others(28): Show |
33 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.205+4824A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94226583 | |||||||
| chr1:94226820 | T | C | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.205+4587A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94226820 | |||||||
| chr1:94226912 | A | G | 31 | a0001c0001t0003g0006 a0001c0001t0003g0033 a0001c0002t0001g0134 others(28): Show |
33 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.205+4495T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94226912 | |||||||
| chr1:94227128 | AT | A | 126 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(123): Show |
145 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.205+4278delA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94227128 | |||||||
| chr1:94227518 | T | C | 1 | a0001c0001t0007g0236 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.205+3889A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94227518 | |||||||
| chr1:94227589 | T | C | 252 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(249): Show |
289 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.205+3818A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94227589 | |||||||
| chr1:94228024 | G | C | 1 | a0001c0001t0004g0237 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.205+3383C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94228024 | |||||||
| chr1:94228147 | C | T | 87 | a0001c0001t0001g0054 a0001c0001t0001g0066 a0001c0001t0001g0095 others(84): Show |
96 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.205+3260G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94228147 | |||||||
| chr1:94228148 | G | A | 1 | a0001c0001t0010g0238 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.205+3259C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94228148 | |||||||
| chr1:94228480 | C | A | 1 | a0001c0001t0001g0239 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.205+2927G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94228480 | |||||||
| chr1:94228584 | C | T | 1 | a0001c0001t0036g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.205+2823G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94228584 | |||||||
| chr1:94228799 | T | C | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.205+2608A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94228799 | |||||||
| chr1:94229107 | A | G | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.205+2300T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94229107 | |||||||
| chr1:94229158 | G | C | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.205+2249C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94229158 | |||||||
| chr1:94229264 | G | C | 2 | a0001c0002t0001g0134 a0001c0002t0001g0135 |
2 | HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.205+2143C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94229264 | |||||||
| chr1:94229265 | C | T | 2 | a0001c0002t0001g0134 a0001c0002t0001g0135 |
2 | HG01975.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.205+2142G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94229265 | |||||||
| chr1:94229612 | C | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(255): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.205+1795G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94229612 | |||||||
| chr1:94229684 | TCCATACA others(4): Show |
T | 1 | a0001c0001t0017g0252 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.205+1712_205+1722d others(13): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94229684 | |||||||
| chr1:94230200 | T | C | 1 | a0001c0001t0013g0280 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.205+1207A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230200 | |||||||
| chr1:94230505 | CTTAAA | C | 23 | a0001c0001t0001g0129 a0001c0001t0003g0131 a0001c0001t0003g0132 others(20): Show |
31 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.205+897_205+901del others(5): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230505 | |||||||
| chr1:94230574 | A | G | 1 | a0001c0001t0004g0100 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.205+833T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230574 | |||||||
| chr1:94230583 | T | C | 44 | a0001c0001t0001g0008 a0001c0001t0001g0287 a0001c0001t0002g0260 others(41): Show |
50 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.205+824A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230583 | |||||||
| chr1:94230594 | A | C | 1 | a0001c0001t0036g0031 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.205+813T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230594 | |||||||
| chr1:94230657 | G | A | 20 | a0001c0001t0001g0129 a0001c0001t0003g0131 a0001c0001t0003g0132 others(17): Show |
28 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.205+750C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230657 | |||||||
| chr1:94230687 | T | C | 2 | a0001c0001t0007g0037 a0001c0001t0007g0038 |
2 | HG01952.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.205+720A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230687 | |||||||
| chr1:94230757 | C | T | 2 | a0001c0001t0004g0010 a0001c0001t0029g0056 |
3 | NA19004.hp2 NA19009.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.205+650G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230757 | |||||||
| chr1:94230930 | G | A | 1 | a0001c0002t0001g0240 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.205+477C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230930 | |||||||
| chr1:94230958 | T | TA | 11 | a0001c0001t0001g0008 a0001c0001t0001g0242 a0001c0001t0001g0287 others(8): Show |
13 | HG00438.hp2 HG00544.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.205+448dupT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230958 | |||||||
| chr1:94230958 | TA | T | 6 | a0001c0001t0001g0054 a0001c0001t0003g0009 a0001c0001t0003g0055 others(3): Show |
7 | HG03831.hp2 NA18949.hp1 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.205+448delT | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94230958 | |||||||
| chr1:94231050 | T | C | 1 | a0002c0003t0024g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.205+357A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94231050 | |||||||
| chr1:94231141 | G | A | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.205+266C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94231141 | |||||||
| chr1:94231188 | A | G | 20 | a0001c0001t0001g0129 a0001c0001t0003g0131 a0001c0001t0003g0132 others(17): Show |
28 | HG00408.hp1 HG00423.hp1 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.205+219T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94231188 | |||||||
| chr1:94231195 | T | C | 1 | a0001c0002t0001g0243 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.205+212A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94231195 | |||||||
| chr1:94231349 | C | T | 1 | a0001c0001t0005g0117 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.205+58G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2/22 | chr1 | 94231349 | |||||||
| chr1:94231887 | T | C | 1 | a0002c0003t0024g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-32-244A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94231887 | |||||||
| chr1:94232024 | C | G | 63 | a0001c0001t0001g0054 a0001c0001t0001g0066 a0001c0001t0001g0095 others(60): Show |
71 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-32-381G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94232024 | |||||||
| chr1:94232193 | A | G | 90 | a0001c0001t0001g0054 a0001c0001t0001g0066 a0001c0001t0001g0095 others(87): Show |
99 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-32-550T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94232193 | |||||||
| chr1:94232202 | T | C | 1 | a0001c0001t0012g0288 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-32-559A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94232202 | |||||||
| chr1:94232263 | G | GATT | 258 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(255): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.-32-623_-32-621dup others(3): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94232263 | |||||||
| chr1:94232573 | G | A | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-32-930C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94232573 | |||||||
| chr1:94232578 | A | G | 3 | a0001c0001t0004g0053 a0002c0003t0015g0051 a0002c0003t0015g0052 |
3 | HG02970.hp1 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-32-935T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94232578 | |||||||
| chr1:94232932 | G | GT | 13 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(10): Show |
13 | HG02135.hp2 HG02300.hp2 HG03130.hp2 others(10): Show |
intron_variant | MODIFIER | c.-32-1290dupA | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94232932 | |||||||
| chr1:94232978 | G | A | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-32-1335C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94232978 | |||||||
| chr1:94233003 | G | A | 1 | a0001c0001t0042g0291 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-32-1360C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233003 | |||||||
| chr1:94233094 | A | G | 44 | a0001c0001t0001g0008 a0001c0001t0001g0287 a0001c0001t0002g0260 others(41): Show |
50 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.-32-1451T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233094 | |||||||
| chr1:94233259 | G | A | 258 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(255): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.-32-1616C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233259 | |||||||
| chr1:94233298 | T | A | 1 | a0001c0002t0001g0245 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-32-1655A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233298 | |||||||
| chr1:94233334 | C | T | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-32-1691G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233334 | |||||||
| chr1:94233411 | T | TAGCAGTA others(1): Show |
256 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(253): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.-32-1769_-32-1768i others(10): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233411 | |||||||
| chr1:94233562 | T | G | 258 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(255): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.-32-1919A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233562 | |||||||
| chr1:94233606 | C | G | 2 | a0001c0001t0022g0041 a0008c0010t0022g0040 |
2 | HG02630.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-32-1963G>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233606 | |||||||
| chr1:94233627 | A | G | 44 | a0001c0001t0001g0008 a0001c0001t0001g0287 a0001c0001t0002g0260 others(41): Show |
50 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.-32-1984T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233627 | |||||||
| chr1:94233743 | A | G | 1 | a0001c0001t0002g0039 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-32-2100T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233743 | |||||||
| chr1:94233777 | G | C | 1 | a0001c0001t0002g0246 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-32-2134C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94233777 | |||||||
| chr1:94234911 | C | A | 2 | a0001c0001t0025g0247 a0001c0001t0025g0248 |
2 | HG01243.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-33+2504G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94234911 | |||||||
| chr1:94234998 | T | C | 2 | a0002c0003t0015g0249 a0002c0003t0015g0250 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-33+2417A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94234998 | |||||||
| chr1:94235090 | T | C | 258 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(255): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.-33+2325A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94235090 | |||||||
| chr1:94235128 | A | G | 4 | a0001c0001t0007g0035 a0001c0001t0007g0036 a0001c0001t0007g0037 others(1): Show |
4 | HG01952.hp1 HG01993.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+2287T>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94235128 | |||||||
| chr1:94235301 | C | A | 1 | a0001c0001t0006g0251 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-33+2114G>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94235301 | |||||||
| chr1:94235322 | C | T | 258 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(255): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(292): Show |
intron_variant | MODIFIER | c.-33+2093G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94235322 | |||||||
| chr1:94235386 | G | A | 1 | a0001c0001t0003g0289 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-33+2029C>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94235386 | |||||||
| chr1:94235653 | C | T | 256 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(253): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.-33+1762G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94235653 | |||||||
| chr1:94235711 | T | C | 2 | a0001c0001t0042g0291 a0001c0001t0043g0290 |
2 | HG03831.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-33+1704A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94235711 | |||||||
| chr1:94235893 | T | C | 1 | a0001c0001t0002g0292 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-33+1522A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94235893 | |||||||
| chr1:94236402 | C | T | 302 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(299): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.-33+1013G>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236402 | |||||||
| chr1:94236530 | G | C | 1 | a0001c0002t0001g0301 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-33+885C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236530 | |||||||
| chr1:94236547 | T | C | 1 | a0001c0001t0002g0302 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-33+868A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236547 | |||||||
| chr1:94236678 | A | C | 1 | a0001c0001t0002g0034 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-33+737T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236678 | |||||||
| chr1:94236683 | A | T | 1 | a0001c0001t0003g0033 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-33+732T>A | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236683 | |||||||
| chr1:94236684 | T | A | 106 | a0001c0001t0001g0048 a0001c0001t0001g0054 a0001c0001t0001g0066 others(103): Show |
116 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-33+731A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236684 | |||||||
| chr1:94236685 | T | A | 1 | a0001c0001t0010g0303 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-33+730A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236685 | |||||||
| chr1:94236693 | T | A | 1 | a0001c0001t0002g0304 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-33+722A>T | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236693 | |||||||
| chr1:94236704 | T | G | 1 | a0001c0001t0037g0305 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-33+711A>C | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236704 | |||||||
| chr1:94236893 | A | C | 2 | a0001c0001t0004g0032 a0001c0001t0036g0031 |
2 | HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-33+522T>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94236893 | |||||||
| chr1:94237121 | G | C | 1 | a0001c0001t0014g0306 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-33+294C>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94237121 | |||||||
| chr1:94237147 | T | C | 6 | a0001c0001t0002g0029 a0001c0001t0002g0308 a0001c0001t0002g0310 others(3): Show |
7 | HG01081.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33+268A>G | ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1/22 | chr1 | 94237147 |