Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 201176 |
| ensemblid | ENSG00000159314.13 |
| hgncid | 31813 |
| symbol | ARHGAP27 |
| name | Rho GTPase activating protein 27 |
| refseq_nuc | NM_001282290.2 |
| refseq_prot | NP_001269219.1 |
| ensembl_nuc | ENST00000685559.1 |
| ensembl_prot | ENSP00000509127.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 45393908 |
| end | 45432870 |
| strand | - |
| ver | v1.2 |
| region | chr17:45393908-45432870 |
| region5000 | chr17:45388908-45437870 |
| regionname0 | ARHGAP27_chr17_45393908_45432870 |
| regionname5000 | ARHGAP27_chr17_45388908_45437870 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 889 | 181 | 42 | 36 | 69 | 9 | 24 | 56 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | MAADV others(884): Show |
chr17 | 45388908 | 45437870 |
| a0002 | 0/0 | 889 | 101 | 29 | 17 | 43 | 3 | 9 | 36 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | MAADV others(884): Show |
chr17 | 45388908 | 45437870 |
| a0003 | 0/0 | 889 | 31 | 5 | 6 | 20 | 0 | 0 | 15 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | MAADV others(884): Show |
chr17 | 45388908 | 45437870 |
| a0004 | 0/0 | 889 | 20 | 1 | 8 | 1 | 4 | 6 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | MAADV others(884): Show |
chr17 | 45388908 | 45437870 |
| a0005 | 0/0 | 889 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | MAADV others(884): Show |
chr17 | 45388908 | 45437870 |
| a0006 | 0/0 | 889 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | MAADV others(884): Show |
chr17 | 45388908 | 45437870 |
| a0007 | 0/0 | 889 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | MAADV others(884): Show |
chr17 | 45388908 | 45437870 |
| a0008 | 0/0 | 889 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | MAADV others(884): Show |
chr17 | 45388908 | 45437870 |
| a0009 | 0/0 | 889 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | MAADV others(884): Show |
chr17 | 45388908 | 45437870 |
| a0010 | 0/0 | 889 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | MAADV others(884): Show |
chr17 | 45388908 | 45437870 |
| a0011 | 0/0 | 889 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | MAADV others(884): Show |
chr17 | 45388908 | 45437870 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2667 | 177 | 38 | 36 | 69 | 9 | 24 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | ATGGC others(2662): Show |
chr17 | 45388908 | 45437870 | ||
| a0001c0009 | 0/0 | 2667 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | ATGGC others(2662): Show |
chr17 | 45388908 | 45437870 | ||
| a0001c0015 | 0/0 | 2667 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | ATGGC others(2662): Show |
chr17 | 45388908 | 45437870 | ||
| a0001c0016 | 0/0 | 2667 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | ATGGC others(2662): Show |
chr17 | 45388908 | 45437870 | ||
| a0002c0002 | 0/0 | 2667 | 99 | 29 | 17 | 41 | 3 | 9 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | ATGGC others(2662): Show |
chr17 | 45388908 | 45437870 | ||
| a0002c0010 | 0/0 | 2667 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | ATGGC others(2662): Show |
chr17 | 45388908 | 45437870 | ||
| a0002c0011 | 0/0 | 2667 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | ATGGC others(2662): Show |
chr17 | 45388908 | 45437870 | ||
| a0003c0003 | 0/0 | 2667 | 28 | 2 | 6 | 20 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | ATGGC others(2662): Show |
chr17 | 45388908 | 45437870 | ||
| a0003c0007 | 0/0 | 2667 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | ATGGC others(2662): Show |
chr17 | 45388908 | 45437870 | ||
| a0004c0004 | 0/0 | 2667 | 20 | 1 | 8 | 1 | 4 | 6 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | ATGGC others(2662): Show |
chr17 | 45388908 | 45437870 | ||
| a0005c0006 | 0/0 | 2667 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | ATGGC others(2662): Show |
chr17 | 45388908 | 45437870 | ||
| a0006c0005 | 0/0 | 2667 | 4 | 0 | 4 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | ATGGC others(2662): Show |
chr17 | 45388908 | 45437870 | ||
| a0007c0008 | 0/0 | 2667 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | ATGGC others(2662): Show |
chr17 | 45388908 | 45437870 | ||
| a0008c0017 | 0/0 | 2667 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | ATGGC others(2662): Show |
chr17 | 45388908 | 45437870 | ||
| a0009c0014 | 0/0 | 2667 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | ATGGC others(2662): Show |
chr17 | 45388908 | 45437870 | ||
| a0010c0013 | 0/0 | 2667 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | ATGGC others(2662): Show |
chr17 | 45388908 | 45437870 | ||
| a0011c0012 | 0/0 | 2667 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | ATGGC others(2662): Show |
chr17 | 45388908 | 45437870 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4621 | 12 | 7 | 0 | 2 | 2 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0001c0001t0002 | 0/0 | 4621 | 70 | 3 | 10 | 47 | 3 | 7 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0001c0001t0003 | 0/1 | 4621 | 52 | 9 | 17 | 11 | 1 | 13 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0001c0001t0005 | 0/0 | 4621 | 15 | 5 | 3 | 4 | 2 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0001c0001t0006 | 0/0 | 4621 | 10 | 7 | 3 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0001c0001t0007 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0001c0001t0008 | 0/0 | 4621 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0001c0001t0009 | 0/0 | 4621 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0001c0001t0010 | 0/0 | 4621 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0001c0001t0011 | 0/0 | 4621 | 3 | 0 | 0 | 2 | 1 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0001c0001t0013 | 0/0 | 4593 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4588): Show |
chr17 | 45388908 | 45437870 |
| a0001c0001t0017 | 0/0 | 4621 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0001c0001t0019 | 0/0 | 4621 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0001c0001t0020 | 0/0 | 4621 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0001c0001t0022 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0001c0001t0023 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0001c0001t0024 | 0/0 | 4621 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0001c0009t0012 | 0/0 | 4621 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0001c0015t0009 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0001c0016t0016 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0002c0002t0001 | 0/0 | 4621 | 70 | 26 | 10 | 25 | 2 | 7 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0002c0002t0002 | 0/0 | 4621 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0002c0002t0003 | 0/0 | 4621 | 17 | 0 | 2 | 14 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0002c0002t0005 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0002c0002t0007 | 0/0 | 4621 | 4 | 1 | 3 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0002c0002t0008 | 0/0 | 4621 | 4 | 1 | 2 | 0 | 1 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0002c0002t0018 | 0/0 | 4621 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0002c0002t0021 | 0/0 | 4621 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0002c0010t0001 | 0/0 | 4621 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0002c0011t0001 | 0/0 | 4621 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0003c0003t0001 | 0/0 | 4621 | 26 | 2 | 5 | 19 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0003c0003t0007 | 0/0 | 4621 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0003c0003t0008 | 0/0 | 4621 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0003c0007t0001 | 0/0 | 4621 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0004c0004t0004 | 0/0 | 4621 | 19 | 1 | 8 | 1 | 4 | 5 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0004c0004t0014 | 0/0 | 4621 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0005c0006t0001 | 0/0 | 4621 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0005c0006t0009 | 0/0 | 4621 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0005c0006t0015 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0006c0005t0002 | 0/0 | 4621 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0006c0005t0003 | 0/0 | 4621 | 3 | 0 | 3 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0007c0008t0001 | 0/0 | 4621 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0008c0017t0025 | 0/0 | 4621 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0009c0014t0001 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0010c0013t0001 | 0/0 | 4621 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| a0011c0012t0001 | 0/0 | 4621 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | GTTGA others(4616): Show |
chr17 | 45388908 | 45437870 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0002 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0016 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0273 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0005g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0006g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0006g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0006g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0006g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0008g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0009g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0010g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0010g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0010g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0011g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0011g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0011g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0013g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0017g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0019g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0020g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0022g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0023g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0001t0024g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0009t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0009t0012g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0015t0009g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0001c0016t0016g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0003g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0007g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0007g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0007g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0008g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0008g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0008g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0018g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0002t0021g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0010t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0002c0011t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0007g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0003t0008g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0007t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0007t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0003c0007t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0004c0004t0004g0001 | 0/0 | 8 | 0 | 3 | 0 | 2 | 3 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0004c0004t0004g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0004c0004t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0004c0004t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0004c0004t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0004c0004t0004g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0004c0004t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0004c0004t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0004c0004t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0004c0004t0004g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0004c0004t0004g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0004c0004t0014g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0005c0006t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0005c0006t0009g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0005c0006t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0005c0006t0015g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0006c0005t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0006c0005t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0006c0005t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0006c0005t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0007c0008t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0007c0008t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0008c0017t0025g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0009c0014t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0010c0013t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| a0011c0012t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0207 | EUR | GBR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0052 | EUR | GBR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0291 | EUR | GBR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00140 | hp2 | a0004 | c0004 | t0004 | g0161 | EUR | GBR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0284 | EUR | FIN | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | FIN | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00323 | hp1 | a0002 | c0002 | t0008 | g0061 | EUR | FIN | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0254 | EUR | FIN | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00597 | hp1 | a0001 | c0001 | t0011 | g0219 | EAS | CHS | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | CHS | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | CHS | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00609 | hp2 | a0003 | c0003 | t0001 | g0139 | EAS | CHS | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00621 | hp1 | a0003 | c0003 | t0007 | g0114 | EAS | CHS | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00621 | hp2 | a0003 | c0003 | t0001 | g0118 | EAS | CHS | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00639 | hp1 | a0003 | c0003 | t0008 | g0120 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0124 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00642 | hp1 | a0002 | c0002 | t0007 | g0087 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0179 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | CHS | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00673 | hp2 | a0001 | c0001 | t0011 | g0268 | EAS | CHS | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0200 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0157 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00738 | hp1 | a0003 | c0003 | t0001 | g0136 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0204 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01071 | hp2 | a0001 | c0001 | t0006 | g0009 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0208 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01074 | hp2 | a0004 | c0004 | t0004 | g0001 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01081 | hp1 | a0002 | c0002 | t0007 | g0085 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0224 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01099 | hp2 | a0004 | c0004 | t0004 | g0163 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01106 | hp1 | a0003 | c0003 | t0001 | g0137 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0180 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0236 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01109 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0025 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01167 | hp2 | a0004 | c0004 | t0004 | g0011 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0125 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01168 | hp2 | a0002 | c0002 | t0007 | g0086 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0100 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01169 | hp2 | a0001 | c0001 | t0006 | g0024 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0155 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0303 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01243 | hp1 | a0001 | c0001 | t0010 | g0019 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0249 | AMR | PUR | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01255 | hp1 | a0002 | c0002 | t0003 | g0003 | AMR | CLM | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01255 | hp2 | a0004 | c0004 | t0004 | g0160 | AMR | CLM | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0275 | AMR | CLM | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01256 | hp2 | a0002 | c0002 | t0008 | g0057 | AMR | CLM | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0276 | AMR | CLM | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01258 | hp2 | a0001 | c0001 | t0009 | g0228 | AMR | CLM | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0033 | AMR | CLM | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01346 | hp2 | a0001 | c0001 | t0005 | g0211 | AMR | CLM | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | CLM | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0058 | AMR | CLM | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01361 | hp1 | a0004 | c0004 | t0004 | g0001 | AMR | CLM | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | CLM | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01433 | hp1 | a0004 | c0004 | t0004 | g0159 | AMR | CLM | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0287 | AMR | CLM | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01496 | hp1 | a0002 | c0002 | t0008 | g0032 | AMR | CLM | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | CLM | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0053 | EUR | IBS | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | IBS | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01516 | hp1 | a0004 | c0004 | t0004 | g0164 | EUR | IBS | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01516 | hp2 | a0001 | c0001 | t0011 | g0256 | EUR | IBS | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01517 | hp1 | a0004 | c0004 | t0004 | g0001 | EUR | IBS | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0214 | EUR | IBS | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0238 | AFR | ACB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0040 | AFR | ACB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0093 | AFR | ACB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01891 | hp2 | a0005 | c0006 | t0009 | g0192 | AFR | ACB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01934 | hp1 | a0006 | c0005 | t0003 | g0149 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01943 | hp1 | a0005 | c0006 | t0001 | g0262 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0227 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01952 | hp2 | a0004 | c0004 | t0004 | g0001 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01975 | hp1 | a0006 | c0005 | t0003 | g0147 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01978 | hp2 | a0003 | c0003 | t0001 | g0117 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0293 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0034 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0060 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02004 | hp2 | a0006 | c0005 | t0003 | g0148 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02027 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | KHV | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0247 | AFR | ACB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02055 | hp2 | a0002 | c0002 | t0008 | g0059 | AFR | ACB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02074 | hp1 | a0003 | c0003 | t0001 | g0089 | EAS | KHV | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | KHV | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | KHV | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02129 | hp2 | a0008 | c0017 | t0025 | g0313 | EAS | KHV | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02132 | hp1 | a0002 | c0002 | t0003 | g0070 | EAS | KHV | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | KHV | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0241 | EAS | KHV | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02145 | hp1 | a0001 | c0001 | t0023 | g0023 | AFR | ACB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02145 | hp2 | a0001 | c0009 | t0012 | g0175 | AFR | ACB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0126 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0246 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02155 | hp1 | a0002 | c0002 | t0003 | g0010 | EAS | CDX | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02257 | hp1 | a0004 | c0004 | t0004 | g0158 | AFR | ACB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0187 | AFR | ACB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02273 | hp1 | a0003 | c0003 | t0001 | g0121 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0210 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0151 | AFR | ACB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0069 | AFR | ACB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0274 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0302 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0110 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02300 | hp2 | a0006 | c0005 | t0002 | g0150 | AMR | PEL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02523 | hp1 | a0001 | c0001 | t0008 | g0205 | EAS | KHV | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0306 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02572 | hp2 | a0003 | c0003 | t0001 | g0145 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02602 | hp1 | a0004 | c0004 | t0004 | g0166 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0045 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0028 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02647 | hp1 | a0001 | c0015 | t0009 | g0190 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0202 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0251 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02717 | hp1 | a0005 | c0006 | t0009 | g0193 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02717 | hp2 | a0009 | c0014 | t0001 | g0189 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02735 | hp1 | a0004 | c0004 | t0004 | g0001 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02738 | hp1 | a0001 | c0001 | t0019 | g0215 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0294 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0152 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02818 | hp2 | a0010 | c0013 | t0001 | g0188 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0043 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02886 | hp2 | a0003 | c0007 | t0001 | g0116 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0297 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0296 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02965 | hp1 | a0001 | c0001 | t0022 | g0182 | AFR | ESN | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02965 | hp2 | a0002 | c0002 | t0001 | g0096 | AFR | ESN | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0084 | AFR | ESN | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02970 | hp2 | a0002 | c0002 | t0007 | g0090 | AFR | ESN | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0038 | AFR | ESN | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0008 | AFR | ESN | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03017 | hp1 | a0002 | c0002 | t0003 | g0075 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0217 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03041 | hp2 | a0003 | c0007 | t0001 | g0129 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0308 | AFR | MSL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0042 | AFR | MSL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0046 | AFR | ESN | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0242 | AFR | ESN | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | ESN | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0020 | AFR | ESN | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | ESN | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0243 | AFR | ESN | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0298 | AFR | MSL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0027 | AFR | MSL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | MSL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0039 | AFR | MSL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0054 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03239 | hp2 | a0004 | c0004 | t0004 | g0001 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03453 | hp2 | a0003 | c0007 | t0001 | g0132 | AFR | MSL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | MSL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0048 | AFR | MSL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0201 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0198 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0047 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03540 | hp2 | a0001 | c0016 | t0016 | g0311 | AFR | GWD | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | MSL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03654 | hp1 | a0001 | c0001 | t0013 | g0018 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03654 | hp2 | a0002 | c0002 | t0021 | g0113 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03669 | hp2 | a0011 | c0012 | t0001 | g0037 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0223 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03704 | hp2 | a0004 | c0004 | t0004 | g0001 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0014 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03710 | hp2 | a0004 | c0004 | t0014 | g0167 | SAS | PJL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | BEB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0176 | SAS | BEB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0292 | SAS | BEB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0013 | SAS | BEB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0307 | SAS | BEB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0305 | SAS | BEB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0230 | SAS | BEB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0221 | SAS | BEB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0080 | SAS | STU | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG04199 | hp2 | a0004 | c0004 | t0004 | g0165 | SAS | STU | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0078 | SAS | STU | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0226 | SAS | STU | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0065 | SAS | STU | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | STU | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | CHB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | CHB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18747 | hp2 | a0003 | c0003 | t0001 | g0119 | EAS | CHB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0067 | AFR | YRI | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0072 | AFR | YRI | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18939 | hp1 | a0003 | c0003 | t0001 | g0153 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18943 | hp2 | a0002 | c0011 | t0001 | g0036 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18954 | hp2 | a0002 | c0002 | t0003 | g0083 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18959 | hp2 | a0002 | c0002 | t0003 | g0056 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18960 | hp1 | a0003 | c0003 | t0001 | g0105 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18960 | hp2 | a0002 | c0002 | t0003 | g0062 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18966 | hp1 | a0001 | c0001 | t0017 | g0171 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0209 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18971 | hp1 | a0007 | c0008 | t0001 | g0097 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18972 | hp2 | a0003 | c0003 | t0001 | g0130 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18973 | hp1 | a0003 | c0003 | t0001 | g0142 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18974 | hp1 | a0002 | c0002 | t0003 | g0076 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18974 | hp2 | a0003 | c0003 | t0001 | g0055 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18980 | hp1 | a0002 | c0002 | t0003 | g0071 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18982 | hp1 | a0003 | c0003 | t0001 | g0091 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18983 | hp2 | a0003 | c0003 | t0001 | g0133 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18985 | hp1 | a0003 | c0003 | t0001 | g0103 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18985 | hp2 | a0002 | c0002 | t0003 | g0063 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18988 | hp1 | a0003 | c0003 | t0001 | g0128 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18989 | hp1 | a0003 | c0003 | t0001 | g0134 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18989 | hp2 | a0001 | c0001 | t0024 | g0312 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18990 | hp2 | a0002 | c0002 | t0003 | g0079 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18995 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18997 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19000 | hp1 | a0002 | c0002 | t0003 | g0073 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19004 | hp1 | a0003 | c0003 | t0001 | g0106 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19004 | hp2 | a0001 | c0001 | t0005 | g0216 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19005 | hp2 | a0003 | c0003 | t0001 | g0135 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19006 | hp2 | a0003 | c0003 | t0001 | g0154 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19007 | hp1 | a0002 | c0002 | t0003 | g0064 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0222 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19009 | hp2 | a0002 | c0002 | t0018 | g0115 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19011 | hp1 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0094 | AFR | LWK | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19030 | hp2 | a0001 | c0001 | t0009 | g0177 | AFR | LWK | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | LWK | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | LWK | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19066 | hp2 | a0002 | c0002 | t0003 | g0010 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19080 | hp1 | a0002 | c0010 | t0001 | g0035 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19085 | hp1 | a0004 | c0004 | t0004 | g0162 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19085 | hp2 | a0003 | c0003 | t0001 | g0131 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19086 | hp1 | a0007 | c0008 | t0001 | g0141 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19088 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0068 | AFR | YRI | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0022 | AFR | YRI | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA20129 | hp1 | a0002 | c0002 | t0005 | g0051 | AFR | ASW | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0049 | AFR | ASW | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA20752 | hp1 | a0004 | c0004 | t0004 | g0001 | EUR | TSI | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0220 | EUR | TSI | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0081 | SAS | GIH | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0146 | SAS | GIH | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01123 | hp1 | a0004 | c0004 | t0004 | g0011 | AMR | CLM | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG01123 | hp2 | a0001 | c0001 | t0020 | g0197 | AMR | CLM | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0029 | AFR | ACB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02486 | hp1 | a0003 | c0003 | t0001 | g0041 | AFR | ACB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0235 | AFR | ACB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0026 | AFR | ACB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0169 | AFR | ACB | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0008 | AFR | MSL | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0095 | AFR | USA | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | USA | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA18955 | hp2 | a0003 | c0003 | t0001 | g0140 | EAS | JPT | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | USA | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA20300 | hp2 | a0001 | c0009 | t0012 | g0174 | AFR | USA | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | LWK | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| NA21309 | hp2 | a0005 | c0006 | t0015 | g0191 | AFR | LWK | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0273 | REF | REF | ARHGAP27_chr17_45388908_45437870 | ARHGAP27 | chr17 | 45388908 | 45437870 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45395459 | G | C | 2 | a0003 a0005 |
35 | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(32): Show |
missense_variant | MODERATE | c.2667C>G | p.His889Gln | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 20/20 | 3070/4621 | 2667/2670 | 889/889 | chr17 | 45395459 | |||
| chr17:45395478 | G | A | 1 | a0009 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.2648C>T | p.Ala883Val | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 20/20 | 3051/4621 | 2648/2670 | 883/889 | chr17 | 45395478 | |||
| chr17:45396976 | C | G | 2 | a0009 a0010 |
2 | HG02717.hp2 HG02818.hp2 |
missense_variant | MODERATE | c.1891G>C | p.Gly631Arg | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 14/20 | 2294/4621 | 1891/2670 | 631/889 | chr17 | 45396976 | |||
| chr17:45404053 | G | A | 2 | a0006 a0008 |
5 | HG01934.hp1 HG01975.hp1 HG02004.hp2 others(2): Show |
missense_variant | MODERATE | c.1523C>T | p.Thr508Met | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 10/20 | 1926/4621 | 1523/2670 | 508/889 | chr17 | 45404053 | |||
| chr17:45406047 | C | T | 1 | a0007 | 2 | NA18971.hp1 NA19086.hp1 |
missense_variant | MODERATE | c.694G>A | p.Glu232Lys | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 5/20 | 1097/4621 | 694/2670 | 232/889 | chr17 | 45406047 | |||
| chr17:45429642 | G | C | 6 | a0001 a0004 a0005 others(3): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
missense_variant | MODERATE | c.638C>G | p.Pro213Arg | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/20 | 1041/4621 | 638/2670 | 213/889 | chr17 | 45429642 | |||
| chr17:45429931 | C | T | 1 | a0004 | 20 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
missense_variant | MODERATE | c.349G>A | p.Ala117Thr | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/20 | 752/4621 | 349/2670 | 117/889 | chr17 | 45429931 | |||
| chr17:45430054 | C | T | 1 | a0011 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.226G>A | p.Ala76Thr | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/20 | 629/4621 | 226/2670 | 76/889 | chr17 | 45430054 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45396080 | G | A | 1 | a0003c0007 | 3 | HG02886.hp2 HG03041.hp2 HG03453.hp2 |
synonymous_variant | LOW | c.2289C>T | p.Asp763Asp | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 18/20 | 2692/4621 | 2289/2670 | 763/889 | chr17 | 45396080 | |||
| chr17:45396965 | C | T | 1 | a0001c0015 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.1902G>A | p.Glu634Glu | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 14/20 | 2305/4621 | 1902/2670 | 634/889 | chr17 | 45396965 | |||
| chr17:45403678 | G | A | 1 | a0001c0016 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.1579C>T | p.Leu527Leu | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 11/20 | 1982/4621 | 1579/2670 | 527/889 | chr17 | 45403678 | |||
| chr17:45404652 | C | T | 1 | a0002c0010 | 1 | NA19080.hp1 | synonymous_variant | LOW | c.1278G>A | p.Lys426Lys | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 7/20 | 1681/4621 | 1278/2670 | 426/889 | chr17 | 45404652 | |||
| chr17:45429803 | G | A | 1 | a0001c0009 | 2 | HG02145.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.477C>T | p.Asp159Asp | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/20 | 880/4621 | 477/2670 | 159/889 | chr17 | 45429803 | |||
| chr17:45430037 | G | A | 1 | a0004c0004 | 20 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
synonymous_variant | LOW | c.243C>T | p.Pro81Pro | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/20 | 646/4621 | 243/2670 | 81/889 | chr17 | 45430037 | |||
| chr17:45430079 | C | T | 2 | a0002c0010 a0002c0011 |
2 | NA18943.hp2 NA19080.hp1 |
synonymous_variant | LOW | c.201G>A | p.Leu67Leu | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/20 | 604/4621 | 201/2670 | 67/889 | chr17 | 45430079 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45394064 | T | C | 1 | a0005c0006t0015 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1392A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 20/20 | 1392 | chr17 | 45394064 | ||||||
| chr17:45394115 | G | A | 22 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(19): Show |
137 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*1341C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 20/20 | 1341 | chr17 | 45394115 | ||||||
| chr17:45394123 | G | A | 6 | a0001c0001t0009 a0001c0015t0009 a0004c0004t0004 others(3): Show |
26 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1333C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 20/20 | 1333 | chr17 | 45394123 | ||||||
| chr17:45394334 | C | A | 1 | a0001c0016t0016 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1122G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 20/20 | 1122 | chr17 | 45394334 | ||||||
| chr17:45394338 | T | C | 1 | a0001c0016t0016 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1118A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 20/20 | 1118 | chr17 | 45394338 | ||||||
| chr17:45394393 | G | C | 1 | a0001c0001t0017 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1063C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 20/20 | 1063 | chr17 | 45394393 | ||||||
| chr17:45394702 | G | C | 1 | a0002c0002t0018 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*754C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 20/20 | 754 | chr17 | 45394702 | ||||||
| chr17:45394828 | G | A | 3 | a0001c0001t0022 a0001c0001t0023 a0001c0009t0012 |
4 | HG02145.hp1 HG02145.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*628C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 20/20 | 628 | chr17 | 45394828 | ||||||
| chr17:45394910 | G | A | 1 | a0001c0001t0019 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*546C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 20/20 | 546 | chr17 | 45394910 | ||||||
| chr17:45394955 | A | G | 30 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(27): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
3_prime_UTR_variant | MODIFIER | c.*501T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 20/20 | 501 | chr17 | 45394955 | ||||||
| chr17:45395086 | G | A | 1 | a0001c0001t0020 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*370C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 20/20 | 370 | chr17 | 45395086 | ||||||
| chr17:45395128 | A | G | 1 | a0002c0002t0021 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*328T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 20/20 | 328 | chr17 | 45395128 | ||||||
| chr17:45395129 | C | A | 1 | a0002c0002t0021 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*327G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 20/20 | 327 | chr17 | 45395129 | ||||||
| chr17:45395140 | A | G | 2 | a0001c0001t0022 a0001c0001t0023 |
2 | HG02145.hp1 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*316T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 20/20 | 316 | chr17 | 45395140 | ||||||
| chr17:45395141 | A | G | 10 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0011 others(7): Show |
84 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*315T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 20/20 | 315 | chr17 | 45395141 | ||||||
| chr17:45395371 | G | A | 3 | a0001c0001t0022 a0001c0001t0023 a0001c0009t0012 |
4 | HG02145.hp1 HG02145.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*85C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 20/20 | 85 | chr17 | 45395371 | ||||||
| chr17:45430283 | A | G | 2 | a0004c0004t0004 a0004c0004t0014 |
20 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-4T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/20 | 4 | chr17 | 45430283 | ||||||
| chr17:45431671 | C | A | 3 | a0001c0001t0006 a0001c0001t0010 a0001c0001t0023 |
15 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-69G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/20 | 1392 | chr17 | 45431671 | ||||||
| chr17:45432229 | G | A | 1 | a0001c0001t0024 | 1 | NA18989.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-164C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 2/20 | chr17 | 45432229 | |||||||
| chr17:45432327 | G | A | 1 | a0008c0017t0025 | 1 | HG02129.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-262C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 2/20 | chr17 | 45432327 | |||||||
| chr17:45432814 | GTCCCGCG others(21): Show |
G | 1 | a0001c0001t0013 | 1 | HG03654.hp1 | 5_prime_UTR_variant | MODIFIER | c.-375_-348delGCCGCA others(22): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 1/20 | 2536 | chr17 | 45432814 | ||||||
| chr17:45432819 | G | A | 1 | a0002c0002t0008 | 1 | HG01256.hp2 | 5_prime_UTR_variant | MODIFIER | c.-352C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 1/20 | 2540 | chr17 | 45432819 | ||||||
| chr17:45432821 | G | C | 2 | a0004c0004t0004 a0004c0004t0014 |
20 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-354C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 1/20 | 2542 | chr17 | 45432821 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:45395734 | C | T | 5 | a0001c0001t0001g0295 a0001c0001t0002g0015 a0001c0001t0003g0170 others(2): Show |
6 | HG02717.hp2 HG02818.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.2492+10G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 19/19 | chr17 | 45395734 | |||||||
| chr17:45395911 | C | T | 1 | a0001c0015t0009g0190 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2387-62G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 18/19 | chr17 | 45395911 | |||||||
| chr17:45395916 | G | T | 1 | a0001c0015t0009g0190 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2386+67C>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 18/19 | chr17 | 45395916 | |||||||
| chr17:45395941 | C | G | 12 | a0001c0001t0009g0228 a0004c0004t0004g0001 a0004c0004t0004g0011 others(9): Show |
20 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.2386+42G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 18/19 | chr17 | 45395941 | |||||||
| chr17:45396128 | G | C | 1 | a0003c0003t0001g0135 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2252-11C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 17/19 | chr17 | 45396128 | |||||||
| chr17:45396324 | G | T | 1 | a0001c0016t0016g0311 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2174-40C>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 16/19 | chr17 | 45396324 | |||||||
| chr17:45396335 | G | A | 2 | a0001c0001t0003g0221 a0001c0001t0003g0223 |
2 | HG03704.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2174-51C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 16/19 | chr17 | 45396335 | |||||||
| chr17:45396342 | G | A | 1 | a0002c0002t0001g0054 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2174-58C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 16/19 | chr17 | 45396342 | |||||||
| chr17:45396344 | G | C | 1 | a0001c0001t0003g0308 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2174-60C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 16/19 | chr17 | 45396344 | |||||||
| chr17:45396647 | C | T | 3 | a0005c0006t0009g0192 a0005c0006t0009g0193 a0005c0006t0015g0191 |
3 | HG01891.hp2 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2074+21G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 15/19 | chr17 | 45396647 | |||||||
| chr17:45396860 | G | A | 1 | a0002c0002t0007g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1951+56C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 14/19 | chr17 | 45396860 | |||||||
| chr17:45396872 | G | T | 1 | a0001c0001t0001g0259 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1951+44C>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 14/19 | chr17 | 45396872 | |||||||
| chr17:45397074 | C | G | 134 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0229 others(131): Show |
138 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(135): Show |
intron_variant | MODIFIER | c.1843-50G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 13/19 | chr17 | 45397074 | |||||||
| chr17:45397097 | C | T | 1 | a0005c0006t0009g0192 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1843-73G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 13/19 | chr17 | 45397097 | |||||||
| chr17:45397221 | A | C | 1 | a0001c0001t0009g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1843-197T>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 13/19 | chr17 | 45397221 | |||||||
| chr17:45397302 | C | G | 19 | a0001c0001t0009g0177 a0001c0001t0009g0228 a0001c0015t0009g0190 others(16): Show |
27 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.1843-278G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 13/19 | chr17 | 45397302 | |||||||
| chr17:45397907 | A | G | 4 | a0001c0001t0022g0182 a0001c0001t0023g0023 a0001c0009t0012g0174 others(1): Show |
4 | HG02145.hp1 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1842+42T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 13/19 | chr17 | 45397907 | |||||||
| chr17:45397926 | T | C | 1 | a0001c0001t0005g0241 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1842+23A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 13/19 | chr17 | 45397926 | |||||||
| chr17:45398502 | G | A | 1 | a0008c0017t0025g0313 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1744-455C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45398502 | |||||||
| chr17:45398563 | G | A | 18 | a0001c0001t0009g0177 a0001c0001t0009g0228 a0001c0015t0009g0190 others(15): Show |
26 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.1744-516C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45398563 | |||||||
| chr17:45398597 | G | A | 1 | a0001c0001t0002g0254 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1744-550C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45398597 | |||||||
| chr17:45398733 | CA | C | 170 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(167): Show |
183 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1744-687delT | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45398733 | |||||||
| chr17:45398780 | C | T | 2 | a0002c0002t0001g0068 a0002c0002t0001g0072 |
2 | NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1744-733G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45398780 | |||||||
| chr17:45398882 | A | T | 1 | a0001c0001t0002g0239 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1744-835T>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45398882 | |||||||
| chr17:45398982 | G | A | 1 | a0002c0002t0007g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1744-935C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45398982 | |||||||
| chr17:45399143 | C | T | 1 | a0001c0001t0005g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1744-1096G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399143 | |||||||
| chr17:45399161 | A | T | 134 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0229 others(131): Show |
138 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(135): Show |
intron_variant | MODIFIER | c.1744-1114T>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399161 | |||||||
| chr17:45399227 | T | C | 1 | a0001c0001t0005g0207 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1744-1180A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399227 | |||||||
| chr17:45399240 | T | A | 172 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(169): Show |
185 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.1744-1193A>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399240 | |||||||
| chr17:45399441 | A | G | 13 | a0001c0001t0009g0228 a0004c0004t0004g0001 a0004c0004t0004g0011 others(10): Show |
21 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.1744-1394T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399441 | |||||||
| chr17:45399533 | A | T | 1 | a0001c0001t0009g0228 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1744-1486T>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399533 | |||||||
| chr17:45399591 | C | CAAAGAAA others(3): Show |
1 | a0001c0016t0016g0311 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1744-1554_1744-154 others(14): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399591 | |||||||
| chr17:45399591 | C | CAAAGAAA others(8): Show |
4 | a0001c0009t0012g0174 a0001c0009t0012g0175 a0002c0002t0001g0060 others(1): Show |
4 | HG02004.hp1 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1744-1559_1744-154 others(19): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399591 | |||||||
| chr17:45399591 | C | CAAAGAAA others(13): Show |
5 | a0002c0002t0001g0093 a0002c0002t0001g0094 a0002c0002t0001g0095 others(2): Show |
5 | HG01891.hp1 HG02965.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1744-1564_1744-154 others(24): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399591 | |||||||
| chr17:45399591 | C | CAAAGAAA others(25): Show |
1 | a0003c0003t0001g0155 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1744-1545_1744-154 others(36): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399591 | |||||||
| chr17:45399591 | C | CAAAGAAA others(18): Show |
43 | a0001c0001t0001g0270 a0001c0001t0005g0220 a0001c0001t0022g0182 others(40): Show |
44 | HG00323.hp1 HG01168.hp1 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.1744-1569_1744-154 others(29): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399591 | |||||||
| chr17:45399591 | C | CAAAGAAA others(23): Show |
53 | a0001c0001t0001g0183 a0001c0001t0001g0206 a0001c0001t0001g0214 others(50): Show |
57 | HG00099.hp2 HG00621.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1744-1574_1744-154 others(34): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399591 | |||||||
| chr17:45399591 | C | CAAAGAAA others(28): Show |
40 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(37): Show |
40 | HG00609.hp2 HG00621.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.1744-1545_1744-154 others(39): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399591 | |||||||
| chr17:45399591 | C | CAAAGAAA others(33): Show |
4 | a0002c0002t0001g0152 a0003c0003t0001g0091 a0003c0003t0001g0135 others(1): Show |
4 | HG02818.hp1 HG03669.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.1744-1545_1744-154 others(44): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399591 | |||||||
| chr17:45399591 | C | CAAAGAAA others(43): Show |
2 | a0001c0001t0007g0187 a0009c0014t0001g0189 |
2 | HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1744-1545_1744-154 others(54): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399591 | |||||||
| chr17:45399591 | C | CAAAGAAA others(48): Show |
1 | a0002c0002t0001g0080 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1744-1545_1744-154 others(59): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399591 | |||||||
| chr17:45399591 | CAAAGA | C | 125 | a0001c0001t0002g0002 a0001c0001t0002g0004 a0001c0001t0002g0005 others(122): Show |
150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.1744-1549_1744-154 others(9): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399591 | |||||||
| chr17:45399591 | CAAAGAAA others(3): Show |
C | 1 | a0001c0001t0003g0208 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1744-1554_1744-154 others(14): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399591 | |||||||
| chr17:45399647 | C | G | 1 | a0001c0001t0005g0179 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1744-1600G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399647 | |||||||
| chr17:45399696 | A | G | 1 | a0001c0015t0009g0190 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1744-1649T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399696 | |||||||
| chr17:45399834 | G | A | 1 | a0001c0001t0002g0301 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1744-1787C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399834 | |||||||
| chr17:45399840 | G | A | 9 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(6): Show |
9 | HG02257.hp2 HG02647.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1744-1793C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399840 | |||||||
| chr17:45399991 | A | G | 1 | a0006c0005t0003g0149 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1744-1944T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45399991 | |||||||
| chr17:45400154 | C | A | 1 | a0001c0015t0009g0190 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1744-2107G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45400154 | |||||||
| chr17:45400589 | C | T | 9 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(6): Show |
9 | HG02257.hp2 HG02647.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1743+2125G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45400589 | |||||||
| chr17:45400827 | C | A | 153 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(150): Show |
158 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(155): Show |
intron_variant | MODIFIER | c.1743+1887G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45400827 | |||||||
| chr17:45400879 | C | T | 1 | a0001c0001t0003g0212 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1743+1835G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45400879 | |||||||
| chr17:45400914 | A | AATAATC | 123 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0229 others(120): Show |
127 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.1743+1794_1743+179 others(10): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45400914 | |||||||
| chr17:45400914 | A | AATAATCA others(5): Show |
9 | a0002c0002t0001g0038 a0002c0002t0001g0067 a0002c0002t0001g0068 others(6): Show |
9 | HG01975.hp1 HG02280.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1743+1788_1743+179 others(16): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45400914 | |||||||
| chr17:45400914 | AATAATCA others(5): Show |
A | 1 | a0001c0001t0002g0178 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1743+1788_1743+179 others(16): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45400914 | |||||||
| chr17:45401085 | T | A | 1 | a0005c0006t0009g0193 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1743+1629A>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45401085 | |||||||
| chr17:45401206 | G | T | 4 | a0001c0001t0022g0182 a0001c0001t0023g0023 a0001c0009t0012g0174 others(1): Show |
4 | HG02145.hp1 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1743+1508C>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45401206 | |||||||
| chr17:45401347 | G | A | 154 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(151): Show |
159 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(156): Show |
intron_variant | MODIFIER | c.1743+1367C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45401347 | |||||||
| chr17:45401370 | C | T | 1 | a0001c0001t0009g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1743+1344G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45401370 | |||||||
| chr17:45401526 | T | C | 1 | a0001c0001t0002g0281 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1743+1188A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45401526 | |||||||
| chr17:45401609 | C | T | 1 | a0001c0001t0009g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1743+1105G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45401609 | |||||||
| chr17:45401987 | C | A | 5 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(2): Show |
5 | HG02647.hp2 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1743+727G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45401987 | |||||||
| chr17:45402173 | AGGGAAAG others(6): Show |
A | 1 | a0001c0001t0011g0268 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1743+528_1743+540d others(15): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45402173 | |||||||
| chr17:45402244 | C | T | 4 | a0002c0002t0001g0017 a0002c0002t0001g0296 a0002c0002t0001g0297 others(1): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1743+470G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45402244 | |||||||
| chr17:45402367 | G | A | 1 | a0002c0002t0001g0052 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1743+347C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45402367 | |||||||
| chr17:45402382 | T | C | 19 | a0001c0001t0009g0177 a0001c0001t0009g0228 a0001c0015t0009g0190 others(16): Show |
27 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.1743+332A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45402382 | |||||||
| chr17:45402405 | G | A | 1 | a0001c0001t0009g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1743+309C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | 45402405 | |||||||
| chr17:45403010 | C | T | 1 | a0001c0001t0002g0252 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1639-192G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 11/19 | chr17 | 45403010 | |||||||
| chr17:45403020 | C | A | 1 | a0002c0002t0001g0144 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1639-202G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 11/19 | chr17 | 45403020 | |||||||
| chr17:45403153 | C | G | 4 | a0001c0001t0022g0182 a0001c0001t0023g0023 a0001c0009t0012g0174 others(1): Show |
4 | HG02145.hp1 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1639-335G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 11/19 | chr17 | 45403153 | |||||||
| chr17:45403333 | G | C | 1 | a0002c0002t0001g0144 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1638+286C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 11/19 | chr17 | 45403333 | |||||||
| chr17:45403334 | C | G | 1 | a0002c0002t0001g0144 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1638+285G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 11/19 | chr17 | 45403334 | |||||||
| chr17:45403334 | C | T | 1 | a0003c0003t0001g0140 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1638+285G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 11/19 | chr17 | 45403334 | |||||||
| chr17:45403335 | G | A | 19 | a0001c0001t0009g0177 a0001c0001t0009g0228 a0001c0015t0009g0190 others(16): Show |
27 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.1638+284C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 11/19 | chr17 | 45403335 | |||||||
| chr17:45403393 | C | G | 2 | a0001c0001t0003g0201 a0001c0001t0019g0215 |
2 | HG02738.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1638+226G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 11/19 | chr17 | 45403393 | |||||||
| chr17:45403482 | G | C | 174 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(171): Show |
187 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.1638+137C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 11/19 | chr17 | 45403482 | |||||||
| chr17:45403519 | C | G | 2 | a0002c0002t0001g0100 a0002c0002t0001g0125 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1638+100G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 11/19 | chr17 | 45403519 | |||||||
| chr17:45403545 | C | T | 1 | a0001c0001t0002g0234 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1638+74G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 11/19 | chr17 | 45403545 | |||||||
| chr17:45403575 | A | T | 6 | a0003c0003t0001g0103 a0003c0003t0001g0105 a0003c0003t0001g0118 others(3): Show |
6 | HG00621.hp2 NA18747.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.1638+44T>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 11/19 | chr17 | 45403575 | |||||||
| chr17:45403606 | G | A | 1 | a0001c0015t0009g0190 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1638+13C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 11/19 | chr17 | 45403606 | |||||||
| chr17:45403774 | C | T | 1 | a0001c0001t0002g0237 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1548-65G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 10/19 | chr17 | 45403774 | |||||||
| chr17:45403802 | A | C | 4 | a0002c0002t0001g0093 a0002c0002t0001g0094 a0002c0002t0001g0095 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1548-93T>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 10/19 | chr17 | 45403802 | |||||||
| chr17:45404175 | C | G | 1 | a0001c0001t0003g0202 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1480-79G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 9/19 | chr17 | 45404175 | |||||||
| chr17:45404193 | T | A | 2 | a0001c0001t0002g0254 a0001c0001t0011g0256 |
2 | HG00323.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.1479+76A>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 9/19 | chr17 | 45404193 | |||||||
| chr17:45404234 | C | G | 5 | a0001c0001t0001g0270 a0002c0002t0001g0107 a0002c0002t0001g0108 others(2): Show |
5 | HG02004.hp2 HG02300.hp1 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1479+35G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 9/19 | chr17 | 45404234 | |||||||
| chr17:45404376 | C | G | 1 | a0001c0001t0002g0254 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1414-42G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 8/19 | chr17 | 45404376 | |||||||
| chr17:45404419 | C | T | 1 | a0002c0002t0001g0081 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1413+26G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 8/19 | chr17 | 45404419 | |||||||
| chr17:45404794 | G | A | 1 | a0001c0015t0009g0190 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1249-113C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 6/19 | chr17 | 45404794 | |||||||
| chr17:45404898 | C | T | 1 | a0001c0001t0003g0014 | 2 | HG00280.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1248+26G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 6/19 | chr17 | 45404898 | |||||||
| chr17:45405140 | G | A | 3 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0002c0002t0001g0110 |
3 | HG02300.hp1 NA18969.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1066-34C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 5/19 | chr17 | 45405140 | |||||||
| chr17:45405154 | C | T | 3 | a0001c0001t0010g0008 a0001c0001t0010g0019 a0001c0001t0010g0020 |
4 | HG01243.hp1 HG02976.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1066-48G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 5/19 | chr17 | 45405154 | |||||||
| chr17:45405230 | G | A | 1 | a0002c0002t0001g0081 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1066-124C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 5/19 | chr17 | 45405230 | |||||||
| chr17:45405381 | C | G | 1 | a0001c0001t0003g0221 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1066-275G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 5/19 | chr17 | 45405381 | |||||||
| chr17:45405504 | A | T | 1 | a0002c0002t0018g0115 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1065+172T>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 5/19 | chr17 | 45405504 | |||||||
| chr17:45406169 | GGGGTTTA others(8): Show |
G | 2 | a0001c0001t0001g0194 a0002c0002t0001g0049 |
2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.658-101_658-87delA others(14): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45406169 | |||||||
| chr17:45406185 | C | T | 17 | a0001c0015t0009g0190 a0001c0016t0016g0311 a0004c0004t0004g0001 others(14): Show |
25 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.658-102G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45406185 | |||||||
| chr17:45406378 | C | G | 1 | a0001c0001t0002g0226 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.658-295G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45406378 | |||||||
| chr17:45406408 | G | A | 133 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0229 others(130): Show |
137 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(134): Show |
intron_variant | MODIFIER | c.658-325C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45406408 | |||||||
| chr17:45406536 | T | A | 4 | a0001c0001t0022g0182 a0001c0001t0023g0023 a0001c0009t0012g0174 others(1): Show |
4 | HG02145.hp1 HG02145.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.658-453A>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45406536 | |||||||
| chr17:45406561 | C | G | 1 | a0001c0001t0006g0026 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.658-478G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45406561 | |||||||
| chr17:45406680 | G | T | 1 | a0001c0001t0023g0023 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.658-597C>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45406680 | |||||||
| chr17:45406796 | C | G | 1 | a0003c0003t0001g0055 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.658-713G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45406796 | |||||||
| chr17:45406890 | C | A | 1 | a0002c0002t0001g0104 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.658-807G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45406890 | |||||||
| chr17:45407025 | T | C | 1 | a0001c0001t0003g0306 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.658-942A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407025 | |||||||
| chr17:45407130 | C | T | 18 | a0001c0001t0009g0177 a0001c0015t0009g0190 a0001c0016t0016g0311 others(15): Show |
26 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.658-1047G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407130 | |||||||
| chr17:45407131 | G | A | 5 | a0001c0001t0003g0170 a0001c0001t0003g0172 a0001c0001t0003g0173 others(2): Show |
5 | NA18963.hp1 NA18964.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.658-1048C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407131 | |||||||
| chr17:45407232 | G | T | 34 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(31): Show |
42 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.658-1149C>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407232 | |||||||
| chr17:45407350 | G | C | 1 | a0001c0001t0002g0257 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.658-1267C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407350 | |||||||
| chr17:45407383 | C | T | 2 | a0005c0006t0009g0193 a0005c0006t0015g0191 |
2 | HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.658-1300G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407383 | |||||||
| chr17:45407393 | C | T | 3 | a0002c0002t0001g0107 a0002c0002t0001g0108 a0002c0002t0001g0110 |
3 | HG02300.hp1 NA18969.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.658-1310G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407393 | |||||||
| chr17:45407404 | G | A | 2 | a0001c0001t0006g0024 a0001c0001t0006g0025 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.658-1321C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407404 | |||||||
| chr17:45407516 | T | TTTTC | 11 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(8): Show |
19 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.658-1434_658-1433i others(6): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407516 | |||||||
| chr17:45407518 | T | C | 1 | a0001c0001t0009g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.658-1435A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407518 | |||||||
| chr17:45407519 | C | CT | 7 | a0001c0001t0002g0233 a0001c0001t0002g0239 a0001c0015t0009g0190 others(4): Show |
7 | HG01358.hp1 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.658-1437dupA | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407519 | |||||||
| chr17:45407519 | C | T | 13 | a0001c0001t0009g0177 a0004c0004t0004g0001 a0004c0004t0004g0011 others(10): Show |
21 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.658-1436G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407519 | |||||||
| chr17:45407537 | T | C | 34 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(31): Show |
42 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.658-1454A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407537 | |||||||
| chr17:45407545 | C | T | 1 | a0002c0002t0001g0124 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.658-1462G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407545 | |||||||
| chr17:45407578 | G | A | 1 | a0001c0001t0002g0286 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.658-1495C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407578 | |||||||
| chr17:45407621 | T | G | 4 | a0002c0002t0001g0017 a0002c0002t0001g0296 a0002c0002t0001g0297 others(1): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.658-1538A>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407621 | |||||||
| chr17:45407645 | G | A | 4 | a0002c0002t0001g0017 a0002c0002t0001g0296 a0002c0002t0001g0297 others(1): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.658-1562C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407645 | |||||||
| chr17:45407757 | G | A | 3 | a0003c0003t0001g0128 a0003c0003t0001g0131 a0003c0003t0001g0134 |
3 | NA18988.hp1 NA18989.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.658-1674C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407757 | |||||||
| chr17:45407853 | G | A | 119 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0229 others(116): Show |
123 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.658-1770C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45407853 | |||||||
| chr17:45408003 | CTT | C | 9 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(6): Show |
9 | HG02257.hp2 HG02647.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.658-1922_658-1921d others(4): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45408003 | |||||||
| chr17:45408120 | CA | C | 22 | a0001c0001t0002g0288 a0001c0001t0009g0177 a0001c0015t0009g0190 others(19): Show |
30 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.658-2038delT | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45408120 | |||||||
| chr17:45408185 | T | G | 18 | a0001c0001t0009g0177 a0001c0015t0009g0190 a0001c0016t0016g0311 others(15): Show |
26 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.658-2102A>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45408185 | |||||||
| chr17:45408263 | A | C | 2 | a0003c0003t0001g0130 a0003c0003t0001g0133 |
2 | NA18972.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.658-2180T>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45408263 | |||||||
| chr17:45408265 | G | A | 3 | a0005c0006t0009g0192 a0005c0006t0009g0193 a0005c0006t0015g0191 |
3 | HG01891.hp2 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.658-2182C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45408265 | |||||||
| chr17:45408413 | A | G | 3 | a0005c0006t0009g0192 a0005c0006t0009g0193 a0005c0006t0015g0191 |
3 | HG01891.hp2 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.658-2330T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45408413 | |||||||
| chr17:45408425 | G | A | 138 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(135): Show |
143 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(140): Show |
intron_variant | MODIFIER | c.658-2342C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45408425 | |||||||
| chr17:45408488 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.658-2405G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45408488 | |||||||
| chr17:45408595 | G | A | 1 | a0006c0005t0002g0150 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.658-2512C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45408595 | |||||||
| chr17:45408632 | C | A | 1 | a0002c0002t0008g0059 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.658-2549G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45408632 | |||||||
| chr17:45408743 | C | T | 3 | a0003c0007t0001g0116 a0003c0007t0001g0129 a0003c0007t0001g0132 |
3 | HG02886.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.658-2660G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45408743 | |||||||
| chr17:45408823 | C | T | 4 | a0002c0002t0001g0093 a0002c0002t0001g0094 a0002c0002t0001g0095 others(1): Show |
4 | HG01891.hp1 HG02965.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.658-2740G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45408823 | |||||||
| chr17:45408935 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.658-2852G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45408935 | |||||||
| chr17:45409191 | C | T | 1 | a0003c0003t0001g0105 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.658-3108G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45409191 | |||||||
| chr17:45409234 | G | A | 1 | a0003c0003t0001g0137 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.658-3151C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45409234 | |||||||
| chr17:45409296 | C | G | 5 | a0001c0001t0022g0182 a0001c0001t0023g0023 a0003c0007t0001g0116 others(2): Show |
5 | HG02145.hp1 HG02886.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.658-3213G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45409296 | |||||||
| chr17:45409416 | T | C | 1 | a0001c0001t0002g0232 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.658-3333A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45409416 | |||||||
| chr17:45409562 | G | A | 1 | a0001c0001t0003g0306 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.658-3479C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45409562 | |||||||
| chr17:45409571 | C | T | 1 | a0001c0015t0009g0190 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.658-3488G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45409571 | |||||||
| chr17:45409672 | T | G | 1 | a0001c0001t0005g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.658-3589A>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45409672 | |||||||
| chr17:45409851 | G | A | 14 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(11): Show |
22 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.658-3768C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45409851 | |||||||
| chr17:45409916 | G | C | 267 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(264): Show |
296 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.658-3833C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45409916 | |||||||
| chr17:45410033 | C | T | 1 | a0001c0001t0005g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.658-3950G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45410033 | |||||||
| chr17:45410058 | T | C | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.658-3975A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45410058 | |||||||
| chr17:45410138 | A | G | 3 | a0005c0006t0009g0192 a0005c0006t0009g0193 a0005c0006t0015g0191 |
3 | HG01891.hp2 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.658-4055T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45410138 | |||||||
| chr17:45410198 | C | T | 2 | a0001c0001t0010g0008 a0001c0001t0010g0019 |
3 | HG01243.hp1 HG02976.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.658-4115G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45410198 | |||||||
| chr17:45410208 | C | A | 21 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(18): Show |
29 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.658-4125G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45410208 | |||||||
| chr17:45410239 | G | T | 15 | a0001c0001t0003g0007 a0001c0001t0003g0195 a0001c0001t0003g0236 others(12): Show |
17 | HG00642.hp2 HG01109.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.658-4156C>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45410239 | |||||||
| chr17:45410529 | G | T | 1 | a0002c0002t0007g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.658-4446C>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45410529 | |||||||
| chr17:45410590 | T | C | 9 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(6): Show |
9 | HG02257.hp2 HG02647.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.658-4507A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45410590 | |||||||
| chr17:45410602 | A | G | 180 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(177): Show |
195 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.658-4519T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45410602 | |||||||
| chr17:45410724 | G | T | 3 | a0001c0001t0002g0265 a0001c0001t0002g0269 a0001c0001t0002g0279 |
3 | NA18955.hp1 NA18972.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.658-4641C>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45410724 | |||||||
| chr17:45410730 | G | A | 1 | a0002c0002t0001g0042 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.658-4647C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45410730 | |||||||
| chr17:45410795 | C | A | 1 | a0001c0001t0005g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.658-4712G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45410795 | |||||||
| chr17:45410873 | T | G | 11 | a0002c0002t0001g0092 a0002c0002t0001g0104 a0002c0002t0001g0111 others(8): Show |
11 | HG00621.hp2 NA18949.hp1 NA18951.hp1 others(8): Show |
intron_variant | MODIFIER | c.658-4790A>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45410873 | |||||||
| chr17:45410946 | C | T | 3 | a0003c0007t0001g0116 a0003c0007t0001g0129 a0003c0007t0001g0132 |
3 | HG02886.hp2 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.658-4863G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45410946 | |||||||
| chr17:45411016 | C | T | 16 | a0002c0002t0001g0101 a0004c0004t0004g0001 a0004c0004t0004g0011 others(13): Show |
24 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.658-4933G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45411016 | |||||||
| chr17:45411115 | G | A | 1 | a0002c0002t0001g0072 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.658-5032C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45411115 | |||||||
| chr17:45411309 | C | T | 1 | a0002c0002t0001g0043 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.658-5226G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45411309 | |||||||
| chr17:45411363 | C | T | 1 | a0001c0001t0009g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.658-5280G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45411363 | |||||||
| chr17:45411426 | T | C | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.658-5343A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45411426 | |||||||
| chr17:45411517 | A | G | 1 | a0001c0016t0016g0311 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.658-5434T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45411517 | |||||||
| chr17:45411698 | G | C | 2 | a0001c0001t0003g0201 a0001c0001t0019g0215 |
2 | HG02738.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.658-5615C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45411698 | |||||||
| chr17:45411748 | C | T | 1 | a0004c0004t0004g0163 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.658-5665G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45411748 | |||||||
| chr17:45411750 | C | A | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.658-5667G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45411750 | |||||||
| chr17:45411795 | T | TCA | 30 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0003g0007 others(27): Show |
34 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.658-5714_658-5713d others(4): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45411795 | |||||||
| chr17:45411795 | T | TCACACA | 12 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(9): Show |
20 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.658-5718_658-5713d others(8): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45411795 | |||||||
| chr17:45411795 | T | TCACACAC others(3): Show |
1 | a0005c0006t0015g0191 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.658-5722_658-5713d others(12): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45411795 | |||||||
| chr17:45411795 | T | TCACACAC others(7): Show |
1 | a0001c0015t0009g0190 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.658-5726_658-5713d others(16): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45411795 | |||||||
| chr17:45411846 | G | C | 1 | a0001c0001t0009g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.658-5763C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45411846 | |||||||
| chr17:45411928 | C | A | 1 | a0001c0001t0005g0207 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.658-5845G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45411928 | |||||||
| chr17:45412139 | T | C | 1 | a0001c0001t0005g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.658-6056A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412139 | |||||||
| chr17:45412257 | C | A | 2 | a0001c0009t0012g0174 a0001c0009t0012g0175 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.658-6174G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412257 | |||||||
| chr17:45412336 | G | C | 1 | a0001c0001t0005g0242 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.658-6253C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412336 | |||||||
| chr17:45412415 | C | T | 14 | a0001c0001t0006g0009 a0001c0001t0006g0021 a0001c0001t0006g0022 others(11): Show |
16 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.658-6332G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412415 | |||||||
| chr17:45412742 | A | C | 1 | a0001c0001t0001g0183 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.658-6659T>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412742 | |||||||
| chr17:45412768 | G | A | 4 | a0002c0002t0001g0017 a0002c0002t0001g0296 a0002c0002t0001g0297 others(1): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.658-6685C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412768 | |||||||
| chr17:45412806 | A | G | 3 | a0001c0001t0002g0265 a0001c0001t0002g0269 a0001c0001t0002g0279 |
3 | NA18955.hp1 NA18972.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.658-6723T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412806 | |||||||
| chr17:45412893 | G | A | 1 | a0001c0001t0005g0238 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.658-6810C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412893 | |||||||
| chr17:45412962 | C | CT | 64 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0229 others(61): Show |
74 | HG00323.hp2 HG00597.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.658-6880dupA | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412962 | |||||||
| chr17:45412962 | C | CTT | 44 | a0001c0001t0001g0270 a0001c0001t0002g0002 a0001c0001t0002g0016 others(41): Show |
50 | HG00609.hp1 HG00642.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.658-6881_658-6880d others(4): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412962 | |||||||
| chr17:45412962 | C | CTTT | 14 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 others(11): Show |
14 | HG00673.hp2 HG01361.hp2 HG02273.hp2 others(11): Show |
intron_variant | MODIFIER | c.658-6882_658-6880d others(5): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412962 | |||||||
| chr17:45412962 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.658-6890_658-6880d others(13): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412962 | |||||||
| chr17:45412962 | CT | C | 71 | a0001c0001t0003g0224 a0001c0001t0003g0243 a0001c0001t0003g0246 others(68): Show |
72 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.658-6880delA | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412962 | |||||||
| chr17:45412962 | CTT | C | 6 | a0001c0001t0003g0218 a0001c0001t0005g0169 a0002c0002t0001g0157 others(3): Show |
6 | HG00735.hp2 HG01975.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.658-6881_658-6880d others(4): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412962 | |||||||
| chr17:45412962 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0009g0177 a0001c0015t0009g0190 |
2 | HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.658-6891_658-6880d others(14): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412962 | |||||||
| chr17:45412962 | CTTTTTTT others(6): Show |
C | 12 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(9): Show |
12 | HG02257.hp2 HG02647.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.658-6892_658-6880d others(15): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412962 | |||||||
| chr17:45412962 | CTTTTTTT others(7): Show |
C | 17 | a0001c0001t0002g0272 a0002c0002t0001g0098 a0002c0010t0001g0035 others(14): Show |
25 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.658-6893_658-6880d others(16): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412962 | |||||||
| chr17:45412962 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0003g0203 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.658-6894_658-6880d others(17): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412962 | |||||||
| chr17:45412962 | CTTTTTTT others(9): Show |
C | 3 | a0001c0001t0003g0227 a0001c0001t0010g0008 a0001c0001t0010g0019 |
4 | HG01243.hp1 HG01952.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.658-6895_658-6880d others(18): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412962 | |||||||
| chr17:45412962 | CTTTTTTT others(10): Show |
C | 1 | a0002c0002t0001g0047 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.658-6896_658-6880d others(19): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45412962 | |||||||
| chr17:45413310 | G | A | 1 | a0002c0002t0001g0157 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.658-7227C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45413310 | |||||||
| chr17:45413324 | C | T | 1 | a0002c0002t0001g0081 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.658-7241G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45413324 | |||||||
| chr17:45413384 | A | G | 1 | a0001c0001t0009g0228 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.658-7301T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45413384 | |||||||
| chr17:45413487 | G | A | 12 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(9): Show |
20 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.658-7404C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45413487 | |||||||
| chr17:45413637 | G | A | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.658-7554C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45413637 | |||||||
| chr17:45413707 | G | A | 9 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(6): Show |
9 | HG02257.hp2 HG02647.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.658-7624C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45413707 | |||||||
| chr17:45413765 | G | C | 2 | a0001c0009t0012g0174 a0001c0009t0012g0175 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.658-7682C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45413765 | |||||||
| chr17:45413975 | G | A | 2 | a0001c0001t0002g0251 a0001c0001t0002g0260 |
2 | HG02683.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.658-7892C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45413975 | |||||||
| chr17:45414105 | CA | C | 176 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(173): Show |
191 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.658-8023delT | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414105 | |||||||
| chr17:45414151 | G | A | 2 | a0001c0009t0012g0174 a0001c0009t0012g0175 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.658-8068C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414151 | |||||||
| chr17:45414225 | C | A | 1 | a0001c0001t0003g0223 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.658-8142G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414225 | |||||||
| chr17:45414293 | C | T | 1 | a0001c0001t0009g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.658-8210G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414293 | |||||||
| chr17:45414442 | G | GT | 8 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0001c0001t0002g0286 others(5): Show |
8 | HG00642.hp2 HG01074.hp1 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.658-8360dupA | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414442 | |||||||
| chr17:45414537 | AAGCAATC others(6): Show |
A | 1 | a0001c0001t0002g0288 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.658-8467_658-8455d others(15): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414537 | |||||||
| chr17:45414612 | A | AT | 16 | a0001c0001t0002g0286 a0004c0004t0004g0001 a0004c0004t0004g0011 others(13): Show |
24 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.658-8530dupA | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414612 | |||||||
| chr17:45414612 | A | ATT | 14 | a0001c0001t0006g0021 a0001c0001t0006g0022 a0001c0001t0006g0024 others(11): Show |
15 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.658-8531_658-8530d others(4): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414612 | |||||||
| chr17:45414612 | AT | A | 118 | a0001c0001t0003g0172 a0001c0001t0003g0218 a0001c0001t0003g0275 others(115): Show |
123 | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.658-8530delA | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414612 | |||||||
| chr17:45414724 | C | T | 1 | a0001c0001t0001g0295 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.658-8641G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414724 | |||||||
| chr17:45414746 | A | G | 3 | a0005c0006t0009g0192 a0005c0006t0009g0193 a0005c0006t0015g0191 |
3 | HG01891.hp2 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.658-8663T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414746 | |||||||
| chr17:45414765 | A | G | 1 | a0001c0001t0003g0294 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.658-8682T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414765 | |||||||
| chr17:45414779 | C | G | 2 | a0001c0001t0002g0263 a0001c0001t0002g0264 |
2 | NA19000.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.658-8696G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414779 | |||||||
| chr17:45414902 | C | CA | 134 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(131): Show |
153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.658-8820dupT | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414902 | |||||||
| chr17:45414902 | C | CAA | 25 | a0001c0001t0001g0229 a0001c0001t0002g0016 a0001c0001t0002g0244 others(22): Show |
26 | HG00597.hp1 HG00597.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.658-8821_658-8820d others(4): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414902 | |||||||
| chr17:45414902 | CA | C | 8 | a0002c0002t0001g0074 a0002c0002t0001g0104 a0002c0002t0001g0122 others(5): Show |
8 | HG03017.hp1 NA18957.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.658-8820delT | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414902 | |||||||
| chr17:45414902 | CAAA | C | 11 | a0004c0004t0004g0001 a0004c0004t0004g0158 a0004c0004t0004g0159 others(8): Show |
18 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.658-8822_658-8820d others(5): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414902 | |||||||
| chr17:45414930 | G | A | 1 | a0001c0001t0003g0012 | 2 | NA18970.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.658-8847C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414930 | |||||||
| chr17:45414991 | C | T | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.658-8908G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45414991 | |||||||
| chr17:45415050 | G | A | 132 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0229 others(129): Show |
151 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.658-8967C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45415050 | |||||||
| chr17:45415062 | C | CA | 12 | a0001c0001t0002g0281 a0001c0001t0003g0014 a0001c0009t0012g0175 others(9): Show |
14 | HG00280.hp2 HG02145.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.658-8980dupT | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45415062 | |||||||
| chr17:45415062 | CA | C | 20 | a0001c0001t0001g0206 a0001c0001t0001g0259 a0001c0001t0002g0231 others(17): Show |
20 | HG00323.hp1 HG01169.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.658-8980delT | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45415062 | |||||||
| chr17:45415260 | A | T | 15 | a0001c0001t0006g0009 a0001c0001t0006g0021 a0001c0001t0006g0022 others(12): Show |
17 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.658-9177T>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45415260 | |||||||
| chr17:45415279 | C | T | 1 | a0001c0016t0016g0311 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.658-9196G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45415279 | |||||||
| chr17:45415360 | G | A | 1 | a0001c0001t0002g0281 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.658-9277C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45415360 | |||||||
| chr17:45415522 | G | A | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.658-9439C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45415522 | |||||||
| chr17:45415735 | G | A | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.658-9652C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45415735 | |||||||
| chr17:45415748 | C | T | 1 | a0001c0001t0003g0246 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.658-9665G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45415748 | |||||||
| chr17:45415832 | T | A | 16 | a0001c0001t0006g0009 a0001c0001t0006g0021 a0001c0001t0006g0022 others(13): Show |
18 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.658-9749A>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45415832 | |||||||
| chr17:45416032 | G | GT | 7 | a0001c0001t0001g0194 a0001c0001t0002g0257 a0001c0001t0002g0288 others(4): Show |
7 | HG01169.hp2 HG03209.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.658-9950dupA | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416032 | |||||||
| chr17:45416032 | G | GTT | 12 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(9): Show |
20 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.658-9951_658-9950d others(4): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416032 | |||||||
| chr17:45416137 | C | A | 15 | a0001c0001t0006g0009 a0001c0001t0006g0021 a0001c0001t0006g0022 others(12): Show |
17 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.658-10054G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416137 | |||||||
| chr17:45416138 | C | T | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.658-10055G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416138 | |||||||
| chr17:45416139 | G | A | 1 | a0001c0016t0016g0311 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.658-10056C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416139 | |||||||
| chr17:45416194 | C | G | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.658-10111G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416194 | |||||||
| chr17:45416222 | A | AT | 6 | a0001c0001t0002g0286 a0001c0001t0005g0220 a0001c0001t0011g0256 others(3): Show |
6 | HG01515.hp1 HG01516.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.658-10140dupA | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416222 | |||||||
| chr17:45416244 | C | G | 2 | a0004c0004t0004g0160 a0004c0004t0004g0161 |
2 | HG00140.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.658-10161G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416244 | |||||||
| chr17:45416244 | C | T | 1 | a0005c0006t0009g0193 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.658-10161G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416244 | |||||||
| chr17:45416344 | G | A | 1 | a0002c0002t0007g0087 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.658-10261C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416344 | |||||||
| chr17:45416432 | C | T | 227 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(224): Show |
257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.658-10349G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416432 | |||||||
| chr17:45416469 | T | C | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.658-10386A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416469 | |||||||
| chr17:45416509 | C | T | 1 | a0001c0001t0006g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.658-10426G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416509 | |||||||
| chr17:45416598 | G | A | 5 | a0001c0001t0003g0170 a0001c0001t0003g0172 a0001c0001t0003g0173 others(2): Show |
5 | NA18963.hp1 NA18964.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.658-10515C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416598 | |||||||
| chr17:45416639 | C | G | 1 | a0001c0001t0003g0204 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.658-10556G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416639 | |||||||
| chr17:45416648 | A | G | 1 | a0002c0002t0007g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.658-10565T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416648 | |||||||
| chr17:45416649 | A | G | 1 | a0002c0002t0008g0057 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.658-10566T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416649 | |||||||
| chr17:45416673 | G | A | 1 | a0002c0002t0001g0146 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.658-10590C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416673 | |||||||
| chr17:45416876 | C | A | 1 | a0001c0001t0005g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.658-10793G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45416876 | |||||||
| chr17:45417131 | A | G | 197 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(194): Show |
227 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.658-11048T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417131 | |||||||
| chr17:45417167 | A | C | 1 | a0003c0003t0001g0089 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.658-11084T>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417167 | |||||||
| chr17:45417316 | T | C | 9 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(6): Show |
9 | HG02257.hp2 HG02647.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.658-11233A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417316 | |||||||
| chr17:45417324 | C | T | 1 | a0006c0005t0003g0147 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.658-11241G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417324 | |||||||
| chr17:45417540 | G | A | 11 | a0001c0001t0001g0229 a0001c0001t0002g0005 a0001c0001t0002g0178 others(8): Show |
14 | HG02027.hp2 NA18942.hp2 NA18949.hp2 others(11): Show |
intron_variant | MODIFIER | c.658-11457C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417540 | |||||||
| chr17:45417596 | G | A | 1 | a0004c0004t0004g0165 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.658-11513C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417596 | |||||||
| chr17:45417753 | C | CA | 5 | a0001c0001t0002g0286 a0002c0002t0001g0017 a0002c0002t0001g0296 others(2): Show |
6 | HG02895.hp2 HG02897.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.658-11671dupT | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417753 | |||||||
| chr17:45417753 | C | CAA | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.658-11672_658-1167 others(6): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417753 | |||||||
| chr17:45417768 | T | A | 1 | a0001c0001t0002g0281 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.658-11685A>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417768 | |||||||
| chr17:45417850 | G | A | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.658-11767C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417850 | |||||||
| chr17:45417869 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.657+11754G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417869 | |||||||
| chr17:45417869 | C | G | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.657+11754G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417869 | |||||||
| chr17:45417968 | G | A | 4 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0002g0291 others(1): Show |
4 | HG00140.hp1 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.657+11655C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417968 | |||||||
| chr17:45417971 | G | C | 4 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0002g0291 others(1): Show |
4 | HG00140.hp1 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.657+11652C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417971 | |||||||
| chr17:45417972 | T | G | 4 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0002g0291 others(1): Show |
4 | HG00140.hp1 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.657+11651A>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417972 | |||||||
| chr17:45417974 | A | G | 4 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0002g0291 others(1): Show |
4 | HG00140.hp1 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.657+11649T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417974 | |||||||
| chr17:45417977 | T | C | 4 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0002g0291 others(1): Show |
4 | HG00140.hp1 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.657+11646A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417977 | |||||||
| chr17:45417979 | G | A | 4 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0002g0291 others(1): Show |
4 | HG00140.hp1 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.657+11644C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417979 | |||||||
| chr17:45417999 | T | C | 1 | a0001c0001t0002g0245 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.657+11624A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45417999 | |||||||
| chr17:45418029 | T | C | 1 | a0003c0003t0001g0128 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.657+11594A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45418029 | |||||||
| chr17:45418036 | CA | C | 7 | a0001c0001t0002g0281 a0001c0001t0003g0199 a0001c0001t0006g0024 others(4): Show |
7 | HG01169.hp2 HG02647.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.657+11586delT | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45418036 | |||||||
| chr17:45418054 | A | T | 23 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(20): Show |
32 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.657+11569T>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45418054 | |||||||
| chr17:45418086 | C | CT | 135 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0229 others(132): Show |
154 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.657+11536dupA | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45418086 | |||||||
| chr17:45418089 | T | TC | 3 | a0001c0001t0003g0246 a0001c0001t0003g0308 a0001c0001t0005g0247 |
3 | HG02055.hp1 HG02148.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.657+11533_657+1153 others(5): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45418089 | |||||||
| chr17:45418173 | G | A | 1 | a0001c0001t0003g0248 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.657+11450C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45418173 | |||||||
| chr17:45418191 | C | T | 1 | a0002c0002t0001g0081 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.657+11432G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45418191 | |||||||
| chr17:45418206 | A | G | 1 | a0001c0001t0003g0196 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.657+11417T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45418206 | |||||||
| chr17:45418271 | T | TA | 19 | a0001c0001t0001g0295 a0001c0001t0002g0279 a0001c0001t0002g0280 others(16): Show |
19 | HG00099.hp2 HG00609.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.657+11351dupT | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45418271 | |||||||
| chr17:45418271 | TA | T | 28 | a0001c0001t0001g0185 a0001c0001t0002g0251 a0001c0001t0002g0252 others(25): Show |
36 | HG00140.hp2 HG00323.hp2 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.657+11351delT | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45418271 | |||||||
| chr17:45418294 | C | T | 138 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0229 others(135): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.657+11329G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45418294 | |||||||
| chr17:45418456 | C | T | 1 | a0001c0001t0002g0301 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.657+11167G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45418456 | |||||||
| chr17:45418486 | A | G | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.657+11137T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45418486 | |||||||
| chr17:45418594 | C | G | 1 | a0002c0002t0021g0113 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.657+11029G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45418594 | |||||||
| chr17:45418852 | G | A | 138 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0229 others(135): Show |
157 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.657+10771C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45418852 | |||||||
| chr17:45418912 | G | A | 1 | a0001c0016t0016g0311 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.657+10711C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45418912 | |||||||
| chr17:45419017 | G | A | 1 | a0001c0001t0002g0281 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.657+10606C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419017 | |||||||
| chr17:45419099 | T | C | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.657+10524A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419099 | |||||||
| chr17:45419137 | C | CACACTAA others(44): Show |
3 | a0005c0006t0009g0192 a0005c0006t0009g0193 a0005c0006t0015g0191 |
3 | HG01891.hp2 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.657+10485_657+1048 others(55): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419137 | |||||||
| chr17:45419462 | C | T | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.657+10161G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419462 | |||||||
| chr17:45419508 | GTATGTAT others(5): Show |
G | 1 | a0002c0002t0001g0049 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.657+10103_657+1011 others(16): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419508 | |||||||
| chr17:45419508 | GTATGTAT others(7): Show |
G | 1 | a0002c0002t0001g0157 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.657+10101_657+1011 others(18): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419508 | |||||||
| chr17:45419508 | GTATGTAT others(11): Show |
G | 2 | a0002c0002t0001g0045 a0002c0002t0001g0046 |
2 | HG02602.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.657+10097_657+1011 others(22): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419508 | |||||||
| chr17:45419508 | GTATGTAT others(13): Show |
G | 11 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0040 others(8): Show |
11 | HG01884.hp2 HG02280.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.657+10095_657+1011 others(24): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419508 | |||||||
| chr17:45419512 | GTA | G | 54 | a0001c0001t0001g0186 a0001c0001t0006g0024 a0001c0001t0006g0025 others(51): Show |
58 | HG00621.hp1 HG00621.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.657+10109_657+1011 others(6): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419512 | |||||||
| chr17:45419512 | GTATA | G | 38 | a0001c0001t0006g0009 a0001c0001t0006g0022 a0001c0001t0010g0019 others(35): Show |
39 | HG00099.hp2 HG00323.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.657+10107_657+1011 others(8): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419512 | |||||||
| chr17:45419512 | GTATATA | G | 15 | a0001c0001t0001g0185 a0001c0001t0001g0304 a0001c0001t0006g0021 others(12): Show |
16 | HG01256.hp2 HG01358.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.657+10105_657+1011 others(10): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419512 | |||||||
| chr17:45419512 | GTATATAT others(1): Show |
G | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0295 others(3): Show |
6 | HG00673.hp1 HG01169.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.657+10103_657+1011 others(12): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419512 | |||||||
| chr17:45419512 | GTATATAT others(3): Show |
G | 2 | a0001c0001t0002g0299 a0001c0001t0002g0300 |
2 | NA18982.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.657+10101_657+1011 others(14): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419512 | |||||||
| chr17:45419512 | GTATATAT others(5): Show |
G | 3 | a0001c0001t0001g0194 a0002c0002t0001g0099 a0002c0002t0001g0298 |
3 | HG03209.hp1 HG03579.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.657+10099_657+1011 others(16): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419512 | |||||||
| chr17:45419512 | GTATATAT others(7): Show |
G | 1 | a0001c0001t0003g0230 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.657+10097_657+1011 others(18): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419512 | |||||||
| chr17:45419512 | GTATATAT others(9): Show |
G | 20 | a0001c0001t0002g0168 a0001c0001t0002g0282 a0001c0001t0002g0283 others(17): Show |
28 | HG00140.hp2 HG00280.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.657+10095_657+1011 others(20): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419512 | |||||||
| chr17:45419512 | GTATATAT others(11): Show |
G | 58 | a0001c0001t0001g0229 a0001c0001t0001g0259 a0001c0001t0001g0270 others(55): Show |
70 | HG00140.hp1 HG00323.hp2 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.657+10093_657+1011 others(22): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419512 | |||||||
| chr17:45419512 | GTATATAT others(13): Show |
G | 65 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0002g0226 others(62): Show |
72 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.657+10091_657+1011 others(24): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419512 | |||||||
| chr17:45419512 | GTATATAT others(15): Show |
G | 1 | a0004c0004t0004g0159 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.657+10089_657+1011 others(26): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419512 | |||||||
| chr17:45419516 | A | G | 11 | a0001c0001t0006g0024 a0001c0001t0006g0025 a0001c0001t0006g0026 others(8): Show |
12 | HG01167.hp1 HG01169.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.657+10107T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419516 | |||||||
| chr17:45419518 | A | G | 6 | a0001c0001t0006g0009 a0001c0001t0006g0022 a0001c0001t0010g0019 others(3): Show |
7 | HG00099.hp2 HG01071.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.657+10105T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419518 | |||||||
| chr17:45419520 | A | G | 1 | a0001c0001t0006g0021 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.657+10103T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419520 | |||||||
| chr17:45419532 | A | G | 11 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(8): Show |
19 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.657+10091T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419532 | |||||||
| chr17:45419534 | A | G | 1 | a0001c0001t0003g0198 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.657+10089T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419534 | |||||||
| chr17:45419538 | A | G | 1 | a0004c0004t0004g0159 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.657+10085T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419538 | |||||||
| chr17:45419635 | A | C | 14 | a0001c0001t0006g0009 a0001c0001t0006g0021 a0001c0001t0006g0022 others(11): Show |
16 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.657+9988T>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419635 | |||||||
| chr17:45419691 | G | C | 1 | a0003c0003t0001g0140 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.657+9932C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419691 | |||||||
| chr17:45419768 | A | G | 1 | a0001c0016t0016g0311 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.657+9855T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419768 | |||||||
| chr17:45419805 | C | A | 1 | a0001c0001t0003g0302 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.657+9818G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419805 | |||||||
| chr17:45419844 | G | A | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.657+9779C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45419844 | |||||||
| chr17:45420029 | T | C | 198 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(195): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.657+9594A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45420029 | |||||||
| chr17:45420118 | C | T | 1 | a0001c0001t0009g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.657+9505G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45420118 | |||||||
| chr17:45420127 | C | T | 2 | a0001c0001t0002g0226 a0001c0001t0005g0200 |
2 | HG00735.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.657+9496G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45420127 | |||||||
| chr17:45420181 | C | G | 4 | a0002c0002t0001g0017 a0002c0002t0001g0296 a0002c0002t0001g0297 others(1): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.657+9442G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45420181 | |||||||
| chr17:45420295 | TTTTTG | T | 133 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0229 others(130): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.657+9323_657+9327d others(7): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45420295 | |||||||
| chr17:45420536 | A | G | 2 | a0002c0002t0001g0296 a0002c0002t0001g0297 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.657+9087T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45420536 | |||||||
| chr17:45420612 | T | C | 182 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(179): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.657+9011A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45420612 | |||||||
| chr17:45420656 | A | T | 1 | a0001c0001t0003g0306 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.657+8967T>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45420656 | |||||||
| chr17:45420720 | T | C | 308 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(305): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.657+8903A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45420720 | |||||||
| chr17:45420729 | C | T | 1 | a0002c0002t0007g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.657+8894G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45420729 | |||||||
| chr17:45420814 | C | T | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.657+8809G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45420814 | |||||||
| chr17:45420815 | A | G | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.657+8808T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45420815 | |||||||
| chr17:45420950 | C | CA | 144 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0259 others(141): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.657+8672dupT | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45420950 | |||||||
| chr17:45420950 | C | CAA | 8 | a0001c0001t0001g0229 a0001c0001t0002g0226 a0001c0001t0002g0287 others(5): Show |
8 | HG01433.hp2 HG01891.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.657+8671_657+8672d others(4): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45420950 | |||||||
| chr17:45420950 | CA | C | 16 | a0001c0001t0006g0009 a0001c0001t0006g0021 a0001c0001t0006g0022 others(13): Show |
18 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.657+8672delT | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45420950 | |||||||
| chr17:45421281 | C | A | 1 | a0001c0001t0003g0227 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.657+8342G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45421281 | |||||||
| chr17:45421328 | C | T | 3 | a0005c0006t0009g0192 a0005c0006t0009g0193 a0005c0006t0015g0191 |
3 | HG01891.hp2 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.657+8295G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45421328 | |||||||
| chr17:45421344 | C | T | 182 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(179): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.657+8279G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45421344 | |||||||
| chr17:45421375 | A | AG | 10 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(7): Show |
10 | HG02257.hp2 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+8247dupC | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45421375 | |||||||
| chr17:45421381 | C | A | 10 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(7): Show |
10 | HG02257.hp2 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+8242G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45421381 | |||||||
| chr17:45421383 | G | C | 10 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(7): Show |
10 | HG02257.hp2 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+8240C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45421383 | |||||||
| chr17:45421385 | G | A | 10 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(7): Show |
10 | HG02257.hp2 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+8238C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45421385 | |||||||
| chr17:45421419 | C | T | 1 | a0001c0001t0020g0197 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.657+8204G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45421419 | |||||||
| chr17:45421962 | T | C | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.657+7661A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45421962 | |||||||
| chr17:45422003 | T | C | 7 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0146 others(4): Show |
7 | HG00642.hp1 HG01081.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.657+7620A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45422003 | |||||||
| chr17:45422250 | C | CA | 18 | a0001c0001t0001g0229 a0001c0001t0006g0029 a0002c0002t0001g0082 others(15): Show |
26 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.657+7372dupT | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45422250 | |||||||
| chr17:45422293 | T | A | 1 | a0001c0001t0001g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.657+7330A>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45422293 | |||||||
| chr17:45422469 | A | C | 1 | a0001c0001t0003g0230 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.657+7154T>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45422469 | |||||||
| chr17:45422473 | A | G | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.657+7150T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45422473 | |||||||
| chr17:45422633 | G | A | 1 | a0002c0002t0007g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.657+6990C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45422633 | |||||||
| chr17:45422668 | G | A | 308 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(305): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.657+6955C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45422668 | |||||||
| chr17:45422684 | A | C | 16 | a0001c0001t0005g0169 a0002c0002t0001g0038 a0002c0002t0001g0039 others(13): Show |
16 | HG00735.hp2 HG01884.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.657+6939T>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45422684 | |||||||
| chr17:45422694 | A | C | 1 | a0001c0001t0001g0229 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.657+6929T>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45422694 | |||||||
| chr17:45422816 | A | G | 1 | a0002c0002t0001g0092 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.657+6807T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45422816 | |||||||
| chr17:45422955 | T | C | 1 | a0003c0003t0001g0145 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.657+6668A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45422955 | |||||||
| chr17:45422978 | G | C | 158 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(155): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.657+6645C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45422978 | |||||||
| chr17:45423011 | T | A | 133 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0229 others(130): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.657+6612A>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45423011 | |||||||
| chr17:45423012 | C | T | 133 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0229 others(130): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.657+6611G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45423012 | |||||||
| chr17:45423111 | G | A | 12 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(9): Show |
20 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.657+6512C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45423111 | |||||||
| chr17:45423121 | C | T | 16 | a0001c0001t0006g0009 a0001c0001t0006g0021 a0001c0001t0006g0022 others(13): Show |
18 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.657+6502G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45423121 | |||||||
| chr17:45423126 | A | G | 2 | a0001c0001t0001g0194 a0001c0001t0009g0177 |
2 | HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.657+6497T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45423126 | |||||||
| chr17:45423207 | C | T | 1 | a0001c0001t0009g0228 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.657+6416G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45423207 | |||||||
| chr17:45423221 | G | A | 25 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(22): Show |
33 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.657+6402C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45423221 | |||||||
| chr17:45423255 | G | A | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.657+6368C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45423255 | |||||||
| chr17:45423378 | T | C | 1 | a0001c0001t0005g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.657+6245A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45423378 | |||||||
| chr17:45423433 | C | G | 13 | a0001c0001t0006g0009 a0001c0001t0006g0021 a0001c0001t0006g0022 others(10): Show |
15 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.657+6190G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45423433 | |||||||
| chr17:45423450 | C | G | 3 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0040 |
3 | HG01884.hp2 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.657+6173G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45423450 | |||||||
| chr17:45423450 | C | T | 3 | a0005c0006t0009g0192 a0005c0006t0009g0193 a0005c0006t0015g0191 |
3 | HG01891.hp2 HG02717.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.657+6173G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45423450 | |||||||
| chr17:45423451 | G | A | 10 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(7): Show |
10 | HG02257.hp2 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+6172C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45423451 | |||||||
| chr17:45423471 | G | A | 133 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0229 others(130): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.657+6152C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45423471 | |||||||
| chr17:45423526 | T | C | 1 | a0002c0002t0003g0083 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.657+6097A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45423526 | |||||||
| chr17:45423704 | T | C | 1 | a0001c0001t0006g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.657+5919A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45423704 | |||||||
| chr17:45423816 | C | T | 46 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0002g0226 others(43): Show |
51 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.657+5807G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45423816 | |||||||
| chr17:45423838 | C | T | 2 | a0001c0009t0012g0174 a0001c0009t0012g0175 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.657+5785G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45423838 | |||||||
| chr17:45424022 | C | T | 16 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0040 others(13): Show |
16 | HG00735.hp2 HG01884.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.657+5601G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45424022 | |||||||
| chr17:45424058 | C | G | 1 | a0001c0016t0016g0311 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.657+5565G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45424058 | |||||||
| chr17:45424076 | T | C | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.657+5547A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45424076 | |||||||
| chr17:45424225 | T | C | 27 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(24): Show |
35 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.657+5398A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45424225 | |||||||
| chr17:45424233 | G | A | 133 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0229 others(130): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.657+5390C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45424233 | |||||||
| chr17:45424265 | G | A | 1 | a0002c0002t0001g0084 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.657+5358C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45424265 | |||||||
| chr17:45424357 | ACCAACAG others(16): Show |
A | 1 | a0004c0004t0014g0167 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.657+5243_657+5265d others(25): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45424357 | |||||||
| chr17:45424404 | A | G | 1 | a0003c0003t0001g0091 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.657+5219T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45424404 | |||||||
| chr17:45424441 | C | T | 1 | a0002c0002t0007g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.657+5182G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45424441 | |||||||
| chr17:45424574 | G | A | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.657+5049C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45424574 | |||||||
| chr17:45424646 | T | A | 4 | a0001c0001t0002g0289 a0001c0001t0002g0290 a0001c0001t0002g0291 others(1): Show |
4 | HG00140.hp1 HG01081.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.657+4977A>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45424646 | |||||||
| chr17:45424646 | T | C | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.657+4977A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45424646 | |||||||
| chr17:45424678 | AG | A | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.657+4944delC | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45424678 | |||||||
| chr17:45424745 | A | G | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.657+4878T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45424745 | |||||||
| chr17:45424779 | C | T | 1 | a0001c0001t0009g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.657+4844G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45424779 | |||||||
| chr17:45424875 | T | C | 15 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(12): Show |
23 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.657+4748A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45424875 | |||||||
| chr17:45424916 | C | T | 1 | a0003c0003t0001g0089 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.657+4707G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45424916 | |||||||
| chr17:45425141 | G | A | 1 | a0001c0001t0003g0293 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.657+4482C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45425141 | |||||||
| chr17:45425218 | C | A | 1 | a0001c0016t0016g0311 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.657+4405G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45425218 | |||||||
| chr17:45425235 | GT | G | 4 | a0002c0002t0001g0017 a0002c0002t0001g0296 a0002c0002t0001g0297 others(1): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.657+4387delA | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45425235 | |||||||
| chr17:45425236 | T | G | 2 | a0002c0002t0001g0088 a0003c0003t0001g0128 |
2 | NA18967.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.657+4387A>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45425236 | |||||||
| chr17:45425237 | G | T | 1 | a0002c0002t0001g0088 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.657+4386C>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45425237 | |||||||
| chr17:45425294 | G | C | 1 | a0001c0016t0016g0311 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.657+4329C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45425294 | |||||||
| chr17:45425354 | G | T | 1 | a0001c0001t0003g0196 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.657+4269C>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45425354 | |||||||
| chr17:45425494 | G | A | 3 | a0002c0002t0007g0085 a0002c0002t0007g0086 a0002c0002t0007g0087 |
3 | HG00642.hp1 HG01081.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.657+4129C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45425494 | |||||||
| chr17:45425525 | C | T | 1 | a0004c0004t0004g0158 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.657+4098G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45425525 | |||||||
| chr17:45425603 | T | C | 1 | a0001c0001t0003g0294 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.657+4020A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45425603 | |||||||
| chr17:45425634 | G | A | 12 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(9): Show |
20 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.657+3989C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45425634 | |||||||
| chr17:45425634 | G | C | 10 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(7): Show |
10 | HG02257.hp2 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.657+3989C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45425634 | |||||||
| chr17:45425766 | G | A | 1 | a0005c0006t0009g0193 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.657+3857C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45425766 | |||||||
| chr17:45425917 | C | T | 133 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0229 others(130): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.657+3706G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45425917 | |||||||
| chr17:45425918 | G | A | 12 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(9): Show |
20 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.657+3705C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45425918 | |||||||
| chr17:45425928 | A | C | 14 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(11): Show |
22 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.657+3695T>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45425928 | |||||||
| chr17:45425990 | C | T | 1 | a0001c0001t0003g0302 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.657+3633G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45425990 | |||||||
| chr17:45426202 | G | A | 1 | a0005c0006t0009g0193 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.657+3421C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45426202 | |||||||
| chr17:45426581 | C | T | 133 | a0001c0001t0001g0206 a0001c0001t0001g0214 a0001c0001t0001g0229 others(130): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.657+3042G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45426581 | |||||||
| chr17:45426621 | A | G | 2 | a0001c0009t0012g0174 a0001c0009t0012g0175 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.657+3002T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45426621 | |||||||
| chr17:45426807 | C | T | 1 | a0001c0001t0003g0195 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.657+2816G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45426807 | |||||||
| chr17:45426851 | C | T | 45 | a0002c0002t0001g0033 a0002c0002t0001g0052 a0002c0002t0001g0053 others(42): Show |
49 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.657+2772G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45426851 | |||||||
| chr17:45426869 | G | A | 1 | a0001c0015t0009g0190 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.657+2754C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45426869 | |||||||
| chr17:45426936 | C | A | 1 | a0002c0002t0001g0146 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.657+2687G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45426936 | |||||||
| chr17:45426936 | C | T | 3 | a0001c0001t0010g0008 a0001c0001t0010g0019 a0001c0001t0010g0020 |
4 | HG01243.hp1 HG02976.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.657+2687G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45426936 | |||||||
| chr17:45426996 | A | T | 1 | a0003c0003t0001g0055 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.657+2627T>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45426996 | |||||||
| chr17:45427059 | C | G | 2 | a0001c0009t0012g0174 a0001c0009t0012g0175 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.657+2564G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45427059 | |||||||
| chr17:45427100 | C | T | 3 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0001g0054 |
3 | HG00099.hp2 HG01515.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.657+2523G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45427100 | |||||||
| chr17:45427102 | C | T | 3 | a0002c0002t0001g0034 a0002c0002t0001g0050 a0002c0002t0005g0051 |
3 | HG01993.hp2 NA18950.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.657+2521G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45427102 | |||||||
| chr17:45427142 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.657+2481G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45427142 | |||||||
| chr17:45427159 | A | AC | 34 | a0001c0001t0005g0169 a0001c0001t0009g0177 a0001c0015t0009g0190 others(31): Show |
42 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(39): Show |
intron_variant | MODIFIER | c.657+2463dupG | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45427159 | |||||||
| chr17:45427674 | T | C | 4 | a0006c0005t0002g0150 a0006c0005t0003g0147 a0006c0005t0003g0148 others(1): Show |
4 | HG01934.hp1 HG01975.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.657+1949A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45427674 | |||||||
| chr17:45428026 | G | A | 1 | a0001c0015t0009g0190 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.657+1597C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45428026 | |||||||
| chr17:45428129 | C | T | 11 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(8): Show |
11 | HG02257.hp2 HG02647.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.657+1494G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45428129 | |||||||
| chr17:45428302 | C | T | 1 | a0001c0001t0005g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.657+1321G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45428302 | |||||||
| chr17:45428413 | C | T | 14 | a0002c0002t0001g0038 a0002c0002t0001g0039 a0002c0002t0001g0040 others(11): Show |
14 | HG00735.hp2 HG01884.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.657+1210G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45428413 | |||||||
| chr17:45428536 | G | T | 1 | a0001c0001t0002g0181 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.657+1087C>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45428536 | |||||||
| chr17:45428561 | G | C | 1 | a0006c0005t0002g0150 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.657+1062C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45428561 | |||||||
| chr17:45428648 | G | A | 1 | a0002c0002t0002g0156 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.657+975C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45428648 | |||||||
| chr17:45428697 | C | CAAAAAAA others(27): Show |
1 | a0001c0001t0001g0295 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.657+925_657+926ins others(34): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45428697 | |||||||
| chr17:45428700 | C | A | 1 | a0001c0001t0001g0295 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.657+923G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45428700 | |||||||
| chr17:45428701 | C | A | 1 | a0001c0001t0001g0295 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.657+922G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45428701 | |||||||
| chr17:45428702 | C | A | 1 | a0001c0001t0001g0295 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.657+921G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45428702 | |||||||
| chr17:45428703 | C | A | 1 | a0001c0001t0001g0295 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.657+920G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45428703 | |||||||
| chr17:45428704 | T | A | 1 | a0001c0001t0001g0295 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.657+919A>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45428704 | |||||||
| chr17:45429047 | C | T | 1 | a0001c0001t0003g0180 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.657+576G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45429047 | |||||||
| chr17:45429176 | G | C | 1 | a0001c0001t0006g0029 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.657+447C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45429176 | |||||||
| chr17:45429317 | A | G | 1 | a0001c0001t0005g0179 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.657+306T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45429317 | |||||||
| chr17:45429408 | G | C | 1 | a0001c0001t0002g0178 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.657+215C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45429408 | |||||||
| chr17:45429437 | G | A | 1 | a0004c0004t0004g0166 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.657+186C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45429437 | |||||||
| chr17:45429540 | C | T | 1 | a0001c0001t0002g0178 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.657+83G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45429540 | |||||||
| chr17:45429583 | C | G | 13 | a0001c0001t0006g0009 a0001c0001t0006g0021 a0001c0001t0006g0022 others(10): Show |
15 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.657+40G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | 45429583 | |||||||
| chr17:45430566 | T | C | 4 | a0002c0002t0001g0017 a0002c0002t0001g0296 a0002c0002t0001g0297 others(1): Show |
5 | HG02895.hp2 HG02897.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-269A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45430566 | |||||||
| chr17:45430589 | C | G | 1 | a0001c0001t0009g0177 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-18-292G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45430589 | |||||||
| chr17:45430598 | G | A | 2 | a0001c0001t0002g0299 a0001c0001t0002g0300 |
2 | NA18982.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-18-301C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45430598 | |||||||
| chr17:45430684 | T | C | 2 | a0002c0002t0001g0151 a0002c0002t0001g0152 |
2 | HG02280.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-18-387A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45430684 | |||||||
| chr17:45430857 | G | T | 12 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(9): Show |
20 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.-18-560C>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45430857 | |||||||
| chr17:45430937 | A | G | 12 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(9): Show |
20 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.-18-640T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45430937 | |||||||
| chr17:45430968 | T | C | 1 | a0001c0001t0002g0301 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-19+653A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45430968 | |||||||
| chr17:45431003 | C | T | 1 | a0001c0001t0003g0176 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-19+618G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45431003 | |||||||
| chr17:45431136 | A | C | 1 | a0002c0002t0001g0034 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-19+485T>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45431136 | |||||||
| chr17:45431153 | A | C | 2 | a0001c0009t0012g0174 a0001c0009t0012g0175 |
2 | HG02145.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-19+468T>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45431153 | |||||||
| chr17:45431203 | A | C | 1 | a0002c0002t0001g0033 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-19+418T>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45431203 | |||||||
| chr17:45431218 | C | A | 1 | a0001c0001t0003g0302 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-19+403G>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45431218 | |||||||
| chr17:45431246 | CAGGGATG others(12): Show |
C | 1 | a0004c0004t0014g0167 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-19+356_-19+374del others(19): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45431246 | |||||||
| chr17:45431250 | G | T | 11 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(8): Show |
19 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.-19+371C>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45431250 | |||||||
| chr17:45431270 | A | G | 1 | a0004c0004t0014g0167 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-19+351T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45431270 | |||||||
| chr17:45431305 | G | GTCTCCGC others(35): Show |
1 | a0004c0004t0014g0167 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-19+315_-19+316ins others(42): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45431305 | |||||||
| chr17:45431306 | G | C | 1 | a0004c0004t0014g0167 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-19+315C>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45431306 | |||||||
| chr17:45431309 | T | C | 1 | a0004c0004t0014g0167 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-19+312A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45431309 | |||||||
| chr17:45431383 | C | T | 5 | a0001c0001t0003g0170 a0001c0001t0003g0172 a0001c0001t0003g0173 others(2): Show |
5 | NA18963.hp1 NA18964.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+238G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3/19 | chr17 | 45431383 | |||||||
| chr17:45431817 | C | G | 1 | a0001c0001t0005g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-150-65G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 2/19 | chr17 | 45431817 | |||||||
| chr17:45431944 | A | G | 12 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(9): Show |
20 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.-150-192T>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 2/19 | chr17 | 45431944 | |||||||
| chr17:45431945 | G | A | 1 | a0001c0001t0003g0303 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-150-193C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 2/19 | chr17 | 45431945 | |||||||
| chr17:45431950 | C | T | 12 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(9): Show |
20 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.-150-198G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 2/19 | chr17 | 45431950 | |||||||
| chr17:45432008 | G | GC | 11 | a0001c0001t0001g0304 a0001c0001t0002g0307 a0001c0001t0002g0309 others(8): Show |
11 | HG01175.hp1 HG02572.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.-151+207dupG | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 2/19 | chr17 | 45432008 | |||||||
| chr17:45432087 | G | A | 1 | a0001c0016t0016g0311 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-151+129C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 2/19 | chr17 | 45432087 | |||||||
| chr17:45432378 | TGGGGAAG others(6): Show |
T | 1 | a0001c0001t0002g0168 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-284-42_-284-30del others(13): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 1/19 | chr17 | 45432378 | |||||||
| chr17:45432412 | C | T | 12 | a0004c0004t0004g0001 a0004c0004t0004g0011 a0004c0004t0004g0158 others(9): Show |
20 | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.-284-63G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 1/19 | chr17 | 45432412 | |||||||
| chr17:45432585 | C | T | 1 | a0002c0002t0008g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-285+167G>A | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 1/19 | chr17 | 45432585 | |||||||
| chr17:45432589 | C | G | 2 | a0002c0002t0001g0030 a0002c0002t0001g0031 |
2 | NA18612.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-285+163G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 1/19 | chr17 | 45432589 | |||||||
| chr17:45432596 | G | A | 1 | a0002c0002t0001g0157 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-285+156C>T | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 1/19 | chr17 | 45432596 | |||||||
| chr17:45432662 | T | C | 182 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(179): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.-285+90A>G | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 1/19 | chr17 | 45432662 | |||||||
| chr17:45432706 | C | G | 13 | a0001c0001t0006g0009 a0001c0001t0006g0021 a0001c0001t0006g0022 others(10): Show |
15 | HG01071.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.-285+46G>C | ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 1/19 | chr17 | 45432706 |