Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57569 |
| ensemblid | ENSG00000137727.13 |
| hgncid | 18357 |
| symbol | ARHGAP20 |
| name | Rho GTPase activating protein 20 |
| refseq_nuc | NM_001384657.1 |
| refseq_prot | NP_001371586.1 |
| ensembl_nuc | ENST00000683387.1 |
| ensembl_prot | ENSP00000507405.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 110577043 |
| end | 110712437 |
| strand | - |
| ver | v1.2 |
| region | chr11:110577043-110712437 |
| region5000 | chr11:110572043-110717437 |
| regionname0 | ARHGAP20_chr11_110577043_110712437 |
| regionname5000 | ARHGAP20_chr11_110572043_110717437 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1191 | 203 | 49 | 40 | 84 | 8 | 20 | 56 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | MEAMS others(1186): Show |
chr11 | 110572043 | 110717437 |
| a0002 | 0/0 | 1191 | 7 | 5 | 1 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | MEAMS others(1186): Show |
chr11 | 110572043 | 110717437 |
| a0003 | 0/0 | 1191 | 3 | 1 | 0 | 0 | 0 | 2 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | MEAMS others(1186): Show |
chr11 | 110572043 | 110717437 |
| a0004 | 0/0 | 1191 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | MEAMS others(1186): Show |
chr11 | 110572043 | 110717437 |
| a0005 | 0/0 | 1191 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | MEAMS others(1186): Show |
chr11 | 110572043 | 110717437 |
| a0006 | 0/0 | 1191 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | MEAMS others(1186): Show |
chr11 | 110572043 | 110717437 |
| a0007 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | MEAMS others(1186): Show |
chr11 | 110572043 | 110717437 |
| a0008 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | MEAMS others(1186): Show |
chr11 | 110572043 | 110717437 |
| a0009 | 0/0 | 1191 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | MEAMS others(1186): Show |
chr11 | 110572043 | 110717437 |
| a0010 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | MEAMS others(1186): Show |
chr11 | 110572043 | 110717437 |
| a0011 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | MEAMS others(1186): Show |
chr11 | 110572043 | 110717437 |
| a0012 | 0/0 | 1191 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | MEAMS others(1186): Show |
chr11 | 110572043 | 110717437 |
| a0013 | 0/0 | 1191 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | MEAMS others(1186): Show |
chr11 | 110572043 | 110717437 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3573 | 187 | 45 | 39 | 76 | 7 | 18 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0001c0002 | 0/0 | 3573 | 8 | 2 | 1 | 3 | 1 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0001c0005 | 0/0 | 3573 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0001c0008 | 0/0 | 3573 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0001c0009 | 0/0 | 3573 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0001c0012 | 0/0 | 3573 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0001c0013 | 0/0 | 3573 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0002c0003 | 0/0 | 3573 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0002c0006 | 0/0 | 3573 | 2 | 1 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0002c0014 | 0/0 | 3573 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0003c0004 | 0/0 | 3573 | 3 | 1 | 0 | 0 | 0 | 2 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0004c0010 | 0/0 | 3573 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0005c0007 | 0/0 | 3573 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0006c0011 | 0/0 | 3573 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0007c0018 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0008c0016 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0009c0021 | 0/0 | 3573 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0010c0020 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0011c0015 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0012c0017 | 0/0 | 3573 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 | ||
| a0013c0019 | 0/0 | 3573 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | ATGGA others(3568): Show |
chr11 | 110572043 | 110717437 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6108 | 70 | 9 | 19 | 28 | 5 | 8 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0001c0001t0002 | 1/0 | 6109 | 49 | 20 | 6 | 18 | 1 | 3 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6104): Show |
chr11 | 110572043 | 110717437 |
| a0001c0001t0003 | 0/0 | 6108 | 38 | 2 | 11 | 19 | 1 | 5 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0001c0001t0004 | 0/0 | 6108 | 9 | 9 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0001c0001t0006 | 0/0 | 6108 | 6 | 4 | 1 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0001c0001t0008 | 0/0 | 6108 | 4 | 0 | 0 | 4 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0001c0001t0009 | 0/0 | 6112 | 3 | 0 | 2 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6107): Show |
chr11 | 110572043 | 110717437 |
| a0001c0001t0011 | 0/0 | 6108 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0001c0001t0013 | 0/0 | 6108 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0001c0001t0014 | 0/0 | 6109 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6104): Show |
chr11 | 110572043 | 110717437 |
| a0001c0001t0016 | 0/0 | 6109 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6104): Show |
chr11 | 110572043 | 110717437 |
| a0001c0001t0018 | 0/0 | 6108 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0001c0001t0021 | 0/0 | 6109 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6104): Show |
chr11 | 110572043 | 110717437 |
| a0001c0002t0005 | 0/0 | 6108 | 8 | 2 | 1 | 3 | 1 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0001c0005t0005 | 0/0 | 6108 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0001c0008t0003 | 0/0 | 6108 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0001c0009t0002 | 0/0 | 6109 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6104): Show |
chr11 | 110572043 | 110717437 |
| a0001c0012t0002 | 0/0 | 6109 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6104): Show |
chr11 | 110572043 | 110717437 |
| a0001c0013t0003 | 0/0 | 6108 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0002c0003t0007 | 0/0 | 6108 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0002c0006t0012 | 0/0 | 6108 | 2 | 1 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0002c0014t0019 | 0/0 | 6109 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6104): Show |
chr11 | 110572043 | 110717437 |
| a0003c0004t0002 | 0/0 | 6109 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6104): Show |
chr11 | 110572043 | 110717437 |
| a0003c0004t0017 | 0/0 | 6109 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6104): Show |
chr11 | 110572043 | 110717437 |
| a0004c0010t0001 | 0/0 | 6108 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0005c0007t0010 | 0/0 | 6109 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6104): Show |
chr11 | 110572043 | 110717437 |
| a0006c0011t0002 | 0/0 | 6109 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6104): Show |
chr11 | 110572043 | 110717437 |
| a0007c0018t0015 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0008c0016t0002 | 0/0 | 6109 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6104): Show |
chr11 | 110572043 | 110717437 |
| a0009c0021t0005 | 0/0 | 6108 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0010c0020t0020 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0011c0015t0004 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| a0012c0017t0002 | 0/0 | 6109 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6104): Show |
chr11 | 110572043 | 110717437 |
| a0013c0019t0004 | 0/0 | 6108 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | GCACT others(6103): Show |
chr11 | 110572043 | 110717437 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0006g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0008g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0008g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0008g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0008g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0009g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0009g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0011g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0011g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0013g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0013g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0014g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0016g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0018g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0001t0021g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0002t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0002t0005g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0002t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0002t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0002t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0002t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0002t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0002t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0005t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0005t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0008t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0008t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0009t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0009t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0012t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0001c0013t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0002c0003t0007g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0002c0003t0007g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0002c0003t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0002c0003t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0002c0006t0012g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0002c0006t0012g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0002c0014t0019g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0003c0004t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0003c0004t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0003c0004t0017g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0004c0010t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0004c0010t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0005c0007t0010g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0005c0007t0010g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0006c0011t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0006c0011t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0007c0018t0015g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0008c0016t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0009c0021t0005g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0010c0020t0020g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0011c0015t0004g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0012c0017t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| a0013c0019t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | GBR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00280 | hp2 | a0001 | c0002 | t0005 | g0206 | EUR | FIN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0056 | EUR | FIN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | CHS | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | CHS | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00639 | hp1 | a0001 | c0001 | t0009 | g0004 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | CHS | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | CHS | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00733 | hp1 | a0001 | c0002 | t0005 | g0113 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00735 | hp1 | a0001 | c0001 | t0009 | g0004 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0081 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0107 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0066 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0102 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01361 | hp1 | a0001 | c0001 | t0006 | g0171 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0125 | EUR | IBS | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | IBS | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01891 | hp1 | a0001 | c0005 | t0005 | g0140 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01952 | hp2 | a0002 | c0014 | t0019 | g0204 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01981 | hp1 | a0004 | c0010 | t0001 | g0159 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02015 | hp1 | a0001 | c0002 | t0005 | g0214 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02015 | hp2 | a0001 | c0001 | t0013 | g0110 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02055 | hp1 | a0002 | c0006 | t0012 | g0111 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02074 | hp2 | a0001 | c0001 | t0018 | g0084 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02080 | hp1 | a0001 | c0002 | t0005 | g0215 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02135 | hp2 | a0001 | c0002 | t0005 | g0208 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02155 | hp1 | a0001 | c0001 | t0011 | g0018 | EAS | CDX | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | CDX | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CDX | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | CDX | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02257 | hp1 | a0002 | c0003 | t0007 | g0148 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0051 | AMR | PEL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02451 | hp2 | a0001 | c0005 | t0005 | g0194 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0090 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02622 | hp2 | a0005 | c0007 | t0010 | g0145 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0067 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02723 | hp1 | a0002 | c0003 | t0007 | g0205 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02809 | hp1 | a0007 | c0018 | t0015 | g0009 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0095 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02922 | hp1 | a0002 | c0003 | t0007 | g0203 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0198 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02970 | hp2 | a0008 | c0016 | t0002 | g0062 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03017 | hp2 | a0002 | c0006 | t0012 | g0138 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0141 | AFR | MSL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03139 | hp2 | a0002 | c0003 | t0007 | g0199 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0202 | AFR | MSL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | MSL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0144 | AFR | MSL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03239 | hp1 | a0001 | c0001 | t0009 | g0118 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03239 | hp2 | a0001 | c0001 | t0016 | g0059 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03491 | hp1 | a0003 | c0004 | t0002 | g0160 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ESN | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03540 | hp2 | a0005 | c0007 | t0010 | g0146 | AFR | GWD | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | MSL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03688 | hp1 | a0003 | c0004 | t0002 | g0142 | SAS | STU | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | STU | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03831 | hp1 | a0009 | c0021 | t0005 | g0217 | SAS | BEB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | BEB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03834 | hp2 | a0001 | c0013 | t0003 | g0068 | SAS | BEB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | BEB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0089 | SAS | BEB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | STU | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0074 | SAS | STU | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG04199 | hp1 | a0001 | c0002 | t0005 | g0213 | SAS | STU | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0121 | SAS | STU | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | CHB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18940 | hp1 | a0001 | c0001 | t0013 | g0187 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18962 | hp1 | a0004 | c0010 | t0001 | g0179 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18972 | hp2 | a0001 | c0001 | t0011 | g0020 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18978 | hp2 | a0001 | c0009 | t0002 | g0193 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18983 | hp1 | a0001 | c0001 | t0006 | g0183 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18997 | hp1 | a0001 | c0001 | t0008 | g0016 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19000 | hp1 | a0001 | c0001 | t0021 | g0177 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19000 | hp2 | a0001 | c0008 | t0003 | g0100 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19002 | hp1 | a0001 | c0009 | t0002 | g0185 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19003 | hp1 | a0001 | c0008 | t0003 | g0099 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19003 | hp2 | a0001 | c0001 | t0008 | g0017 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19030 | hp1 | a0011 | c0015 | t0004 | g0151 | AFR | LWK | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19030 | hp2 | a0003 | c0004 | t0017 | g0143 | AFR | LWK | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | LWK | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | LWK | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19057 | hp2 | a0001 | c0001 | t0008 | g0021 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19067 | hp1 | a0012 | c0017 | t0002 | g0139 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19075 | hp1 | a0001 | c0012 | t0002 | g0186 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19075 | hp2 | a0006 | c0011 | t0002 | g0126 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19084 | hp2 | a0001 | c0001 | t0008 | g0072 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19086 | hp1 | a0006 | c0011 | t0002 | g0030 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19240 | hp1 | a0001 | c0002 | t0005 | g0211 | AFR | YRI | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA19240 | hp2 | a0013 | c0019 | t0004 | g0149 | AFR | YRI | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0092 | AFR | ASW | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA20129 | hp2 | a0001 | c0002 | t0005 | g0212 | AFR | ASW | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0196 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0197 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0154 | AFR | ACB | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG06807 | hp1 | a0010 | c0020 | t0020 | g0147 | AFR | USA | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | USA | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| NA21309 | hp2 | a0001 | c0001 | t0014 | g0008 | AFR | LWK | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0136 | REF | REF | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0079 | REF | REF | ARHGAP20_chr11_110572043_110717437 | ARHGAP20 | chr11 | 110572043 | 110717437 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:110579620 | C | T | 1 | a0008 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.3326G>A | p.Arg1109Lys | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 3532/6109 | 3326/3576 | 1109/1191 | chr11 | 110579620 | |||
| chr11:110579639 | G | C | 2 | a0011 a0013 |
2 | NA19030.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.3307C>G | p.Pro1103Ala | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 3513/6109 | 3307/3576 | 1103/1191 | chr11 | 110579639 | |||
| chr11:110579872 | G | A | 1 | a0012 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.3074C>T | p.Ser1025Leu | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 3280/6109 | 3074/3576 | 1025/1191 | chr11 | 110579872 | |||
| chr11:110580287 | G | A | 1 | a0004 | 2 | HG01981.hp1 NA18962.hp1 |
missense_variant | MODERATE | c.2659C>T | p.Arg887Trp | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 2865/6109 | 2659/3576 | 887/1191 | chr11 | 110580287 | |||
| chr11:110580781 | T | C | 1 | a0006 | 2 | NA19075.hp2 NA19086.hp1 |
missense_variant | MODERATE | c.2165A>G | p.Tyr722Cys | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 2371/6109 | 2165/3576 | 722/1191 | chr11 | 110580781 | |||
| chr11:110580997 | T | G | 3 | a0003 a0005 a0012 |
6 | HG02622.hp2 HG03491.hp1 HG03540.hp2 others(3): Show |
missense_variant | MODERATE | c.1949A>C | p.Gln650Pro | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 2155/6109 | 1949/3576 | 650/1191 | chr11 | 110580997 | |||
| chr11:110583589 | C | T | 3 | a0002 a0005 a0010 |
10 | HG01952.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
missense_variant | MODERATE | c.1564G>A | p.Ala522Thr | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 13/15 | 1770/6109 | 1564/3576 | 522/1191 | chr11 | 110583589 | |||
| chr11:110606665 | G | C | 1 | a0007 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.860C>G | p.Pro287Arg | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/15 | 1066/6109 | 860/3576 | 287/1191 | chr11 | 110606665 | |||
| chr11:110624214 | T | C | 1 | a0013 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.451A>G | p.Met151Val | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/15 | 657/6109 | 451/3576 | 151/1191 | chr11 | 110624214 | |||
| chr11:110690551 | T | C | 1 | a0010 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.184A>G | p.Thr62Ala | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/15 | 390/6109 | 184/3576 | 62/1191 | chr11 | 110690551 | |||
| chr11:110712146 | C | A | 1 | a0009 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.86G>T | p.Gly29Val | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/15 | 292/6109 | 86/3576 | 29/1191 | chr11 | 110712146 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:110579439 | C | T | 1 | a0001c0008 | 2 | NA19000.hp2 NA19003.hp1 |
synonymous_variant | LOW | c.3507G>A | p.Ala1169Ala | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 3713/6109 | 3507/3576 | 1169/1191 | chr11 | 110579439 | |||
| chr11:110579940 | G | A | 2 | a0001c0009 a0008c0016 |
3 | HG02970.hp2 NA18978.hp2 NA19002.hp1 |
synonymous_variant | LOW | c.3006C>T | p.Pro1002Pro | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 3212/6109 | 3006/3576 | 1002/1191 | chr11 | 110579940 | |||
| chr11:110580696 | C | T | 2 | a0002c0006 a0002c0014 |
3 | HG01952.hp2 HG02055.hp1 HG03017.hp2 |
synonymous_variant | LOW | c.2250G>A | p.Gln750Gln | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 2456/6109 | 2250/3576 | 750/1191 | chr11 | 110580696 | |||
| chr11:110581161 | A | G | 4 | a0001c0002 a0001c0005 a0007c0018 others(1): Show |
12 | HG00280.hp2 HG00733.hp1 HG01891.hp1 others(9): Show |
synonymous_variant | LOW | c.1785T>C | p.Asp595Asp | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 1991/6109 | 1785/3576 | 595/1191 | chr11 | 110581161 | |||
| chr11:110582396 | T | G | 1 | a0013c0019 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.1645A>C | p.Arg549Arg | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/15 | 1851/6109 | 1645/3576 | 549/1191 | chr11 | 110582396 | |||
| chr11:110583566 | T | C | 1 | a0002c0014 | 1 | HG01952.hp2 | synonymous_variant | LOW | c.1587A>G | p.Glu529Glu | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 13/15 | 1793/6109 | 1587/3576 | 529/1191 | chr11 | 110583566 | |||
| chr11:110583614 | G | A | 2 | a0002c0003 a0010c0020 |
5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
synonymous_variant | LOW | c.1539C>T | p.Val513Val | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 13/15 | 1745/6109 | 1539/3576 | 513/1191 | chr11 | 110583614 | |||
| chr11:110592031 | A | G | 1 | a0001c0013 | 1 | HG03834.hp2 | synonymous_variant | LOW | c.1089T>C | p.Phe363Phe | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/15 | 1295/6109 | 1089/3576 | 363/1191 | chr11 | 110592031 | |||
| chr11:110624278 | A | T | 1 | a0001c0005 | 2 | HG01891.hp1 HG02451.hp2 |
synonymous_variant | LOW | c.387T>A | p.Ile129Ile | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/15 | 593/6109 | 387/3576 | 129/1191 | chr11 | 110624278 | |||
| chr11:110624296 | A | G | 1 | a0001c0012 | 1 | NA19075.hp1 | synonymous_variant | LOW | c.369T>C | p.Phe123Phe | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/15 | 575/6109 | 369/3576 | 123/1191 | chr11 | 110624296 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:110577231 | C | A | 1 | a0001c0001t0013 | 2 | HG02015.hp2 NA18940.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2139G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 2139 | chr11 | 110577231 | ||||||
| chr11:110577357 | G | T | 1 | a0001c0001t0016 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2013C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 2013 | chr11 | 110577357 | ||||||
| chr11:110577471 | GA | G | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(18): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*1898delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 1898 | chr11 | 110577471 | ||||||
| chr11:110577502 | A | C | 1 | a0001c0001t0011 | 2 | HG02155.hp1 NA18972.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1868T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 1868 | chr11 | 110577502 | ||||||
| chr11:110577616 | T | G | 6 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0009 others(3): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1754A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 1754 | chr11 | 110577616 | ||||||
| chr11:110577654 | G | A | 1 | a0003c0004t0017 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1716C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 1716 | chr11 | 110577654 | ||||||
| chr11:110577960 | G | A | 1 | a0001c0001t0018 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1410C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 1410 | chr11 | 110577960 | ||||||
| chr11:110578165 | G | A | 6 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0011 others(3): Show |
48 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1205C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 1205 | chr11 | 110578165 | ||||||
| chr11:110578317 | G | A | 4 | a0001c0002t0005 a0001c0005t0005 a0007c0018t0015 others(1): Show |
12 | HG00280.hp2 HG00733.hp1 HG01891.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1053C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 1053 | chr11 | 110578317 | ||||||
| chr11:110578395 | G | T | 1 | a0005c0007t0010 | 2 | HG02622.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*975C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 975 | chr11 | 110578395 | ||||||
| chr11:110578481 | G | T | 4 | a0002c0003t0007 a0002c0006t0012 a0002c0014t0019 others(1): Show |
8 | HG01952.hp2 HG02055.hp1 HG02257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*889C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 889 | chr11 | 110578481 | ||||||
| chr11:110578498 | G | C | 1 | a0001c0001t0008 | 4 | NA18997.hp1 NA19003.hp2 NA19057.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*872C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 872 | chr11 | 110578498 | ||||||
| chr11:110578507 | G | GTCTT | 1 | a0001c0001t0009 | 3 | HG00639.hp1 HG00735.hp1 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*859_*862dupAAGA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 862 | chr11 | 110578507 | ||||||
| chr11:110578702 | A | G | 2 | a0002c0003t0007 a0010c0020t0020 |
5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*668T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 668 | chr11 | 110578702 | ||||||
| chr11:110578834 | T | G | 2 | a0002c0006t0012 a0002c0014t0019 |
3 | HG01952.hp2 HG02055.hp1 HG03017.hp2 |
3_prime_UTR_variant | MODIFIER | c.*536A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 536 | chr11 | 110578834 | ||||||
| chr11:110579079 | G | A | 1 | a0010c0020t0020 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*291C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 291 | chr11 | 110579079 | ||||||
| chr11:110579139 | C | A | 5 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0013 others(2): Show |
77 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*231G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 15/15 | 231 | chr11 | 110579139 | ||||||
| chr11:110712314 | G | T | 1 | a0007c0018t0015 | 1 | HG02809.hp1 | 5_prime_UTR_variant | MODIFIER | c.-83C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/15 | 83 | chr11 | 110712314 | ||||||
| chr11:110712388 | G | T | 1 | a0001c0001t0014 | 1 | NA21309.hp2 | 5_prime_UTR_variant | MODIFIER | c.-157C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/15 | 157 | chr11 | 110712388 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:110581289 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0172 a0001c0001t0001g0190 |
4 | HG02622.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1721-64T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110581289 | |||||||
| chr11:110581295 | A | AAACTATG others(11): Show |
10 | a0002c0003t0007g0148 a0002c0003t0007g0199 a0002c0003t0007g0203 others(7): Show |
10 | HG01952.hp2 HG02055.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1721-71_1721-70ins others(18): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110581295 | |||||||
| chr11:110581705 | C | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0019 others(155): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1721-480G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110581705 | |||||||
| chr11:110581815 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1720+506C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110581815 | |||||||
| chr11:110581825 | G | A | 2 | a0006c0011t0002g0030 a0006c0011t0002g0126 |
2 | NA19075.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1720+496C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110581825 | |||||||
| chr11:110581878 | A | G | 8 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(5): Show |
9 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1720+443T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110581878 | |||||||
| chr11:110581897 | G | A | 1 | a0001c0002t0005g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1720+424C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110581897 | |||||||
| chr11:110581930 | C | CA | 6 | a0001c0001t0002g0055 a0001c0001t0002g0201 a0001c0001t0004g0014 others(3): Show |
6 | HG01891.hp2 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1720+390dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110581930 | |||||||
| chr11:110581930 | CA | C | 80 | a0001c0001t0001g0073 a0001c0001t0001g0130 a0001c0001t0002g0026 others(77): Show |
84 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(81): Show |
intron_variant | MODIFIER | c.1720+390delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110581930 | |||||||
| chr11:110582106 | C | T | 158 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0019 others(155): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1720+215G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110582106 | |||||||
| chr11:110582164 | C | T | 2 | a0011c0015t0004g0151 a0013c0019t0004g0149 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1720+157G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110582164 | |||||||
| chr11:110582262 | C | T | 8 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(5): Show |
9 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1720+59G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110582262 | |||||||
| chr11:110582275 | C | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0019 others(154): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1720+46G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110582275 | |||||||
| chr11:110582285 | G | A | 152 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0019 others(149): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1720+36C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 14/14 | chr11 | 110582285 | |||||||
| chr11:110582526 | C | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0019 others(155): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1606-91G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 13/14 | chr11 | 110582526 | |||||||
| chr11:110582815 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1606-380A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 13/14 | chr11 | 110582815 | |||||||
| chr11:110582973 | C | G | 12 | a0001c0002t0005g0113 a0001c0002t0005g0206 a0001c0002t0005g0208 others(9): Show |
12 | HG00280.hp2 HG00733.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1606-538G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 13/14 | chr11 | 110582973 | |||||||
| chr11:110583089 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1605+459G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 13/14 | chr11 | 110583089 | |||||||
| chr11:110583504 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1605+44C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 13/14 | chr11 | 110583504 | |||||||
| chr11:110584028 | G | A | 3 | a0002c0006t0012g0111 a0002c0006t0012g0138 a0002c0014t0019g0204 |
3 | HG01952.hp2 HG02055.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1416-291C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584028 | |||||||
| chr11:110584084 | C | G | 45 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0005 others(42): Show |
49 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1416-347G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584084 | |||||||
| chr11:110584152 | C | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0019 others(77): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1416-415G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584152 | |||||||
| chr11:110584196 | A | G | 6 | a0003c0004t0002g0142 a0003c0004t0002g0160 a0003c0004t0017g0143 others(3): Show |
6 | HG02622.hp2 HG03491.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.1416-459T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584196 | |||||||
| chr11:110584214 | T | C | 8 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(5): Show |
9 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1416-477A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584214 | |||||||
| chr11:110584361 | T | C | 3 | a0001c0001t0006g0196 a0001c0001t0006g0197 a0001c0001t0006g0198 |
3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1416-624A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584361 | |||||||
| chr11:110584649 | C | T | 2 | a0001c0001t0008g0016 a0001c0001t0008g0021 |
2 | NA18997.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1416-912G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584649 | |||||||
| chr11:110584844 | C | CAT | 46 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0005 others(43): Show |
50 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.1416-1109_1416-110 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584844 | |||||||
| chr11:110584861 | A | G | 1 | a0001c0001t0002g0026 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1416-1124T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584861 | |||||||
| chr11:110584876 | T | C | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1416-1139A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584876 | |||||||
| chr11:110584908 | T | TATATATA others(3): Show |
7 | a0002c0003t0007g0148 a0002c0003t0007g0199 a0002c0003t0007g0203 others(4): Show |
7 | HG02257.hp1 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1416-1181_1416-117 others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584908 | |||||||
| chr11:110584908 | T | TATATATG others(1): Show |
45 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0005 others(42): Show |
49 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1416-1172_1416-117 others(12): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584908 | |||||||
| chr11:110584951 | A | ATG | 50 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0005 others(47): Show |
54 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.1416-1216_1416-121 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584951 | |||||||
| chr11:110584961 | G | A | 5 | a0002c0003t0007g0148 a0002c0003t0007g0199 a0002c0003t0007g0203 others(2): Show |
5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1416-1224C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584961 | |||||||
| chr11:110584965 | A | ATATG | 5 | a0002c0003t0007g0148 a0002c0003t0007g0199 a0002c0003t0007g0203 others(2): Show |
5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1416-1229_1416-122 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584965 | |||||||
| chr11:110584966 | T | TATATATG others(9): Show |
2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1416-1230_1416-122 others(20): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584966 | |||||||
| chr11:110584966 | T | TATATGA | 57 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0005 others(54): Show |
62 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.1416-1235_1416-123 others(10): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584966 | |||||||
| chr11:110584966 | T | TATATGTG others(9): Show |
2 | a0011c0015t0004g0151 a0013c0019t0004g0149 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1416-1230_1416-122 others(20): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584966 | |||||||
| chr11:110584969 | A | G | 5 | a0002c0003t0007g0148 a0002c0003t0007g0199 a0002c0003t0007g0203 others(2): Show |
5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1416-1232T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584969 | |||||||
| chr11:110584971 | G | GTGAATAT others(11): Show |
77 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0019 others(74): Show |
81 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1416-1235_1416-123 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584971 | |||||||
| chr11:110584971 | GAATATAT others(15): Show |
G | 1 | a0001c0001t0001g0039 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1415+1223_1416-123 others(26): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584971 | |||||||
| chr11:110584972 | A | T | 77 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0019 others(74): Show |
81 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.1416-1235T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110584972 | |||||||
| chr11:110585018 | CATATATG others(3): Show |
C | 3 | a0002c0006t0012g0138 a0002c0014t0019g0204 a0009c0021t0005g0217 |
3 | HG01952.hp2 HG03017.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1415+1188_1415+119 others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585018 | |||||||
| chr11:110585025 | G | GTGAATAT others(3): Show |
78 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0022 others(75): Show |
81 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.1415+1190_1415+119 others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585025 | |||||||
| chr11:110585025 | G | GTGAATAT others(27): Show |
2 | a0001c0001t0003g0089 a0001c0013t0003g0068 |
2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1415+1190_1415+119 others(38): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585025 | |||||||
| chr11:110585030 | TATATGTG others(11): Show |
T | 1 | a0002c0006t0012g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1415+1168_1415+118 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585030 | |||||||
| chr11:110585032 | T | TATATGA | 43 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0005 others(40): Show |
47 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.1415+1183_1415+118 others(10): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585032 | |||||||
| chr11:110585035 | G | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0078 a0001c0001t0001g0115 others(6): Show |
10 | HG00280.hp1 HG00738.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1415+1181C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585035 | |||||||
| chr11:110585038 | AATAT | A | 3 | a0003c0004t0002g0142 a0003c0004t0002g0160 a0012c0017t0002g0139 |
3 | HG03491.hp1 HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1415+1174_1415+117 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585038 | |||||||
| chr11:110585040 | T | C | 2 | a0001c0001t0003g0089 a0001c0013t0003g0068 |
2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1415+1176A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585040 | |||||||
| chr11:110585040 | T | TATATATG others(21): Show |
1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1415+1148_1415+117 others(32): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585040 | |||||||
| chr11:110585040 | TATATATG others(1): Show |
T | 2 | a0001c0001t0002g0098 a0001c0001t0002g0202 |
2 | HG03209.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1415+1168_1415+117 others(12): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585040 | |||||||
| chr11:110585045 | A | G | 5 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(2): Show |
5 | HG00280.hp1 HG01074.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.1415+1171T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585045 | |||||||
| chr11:110585048 | A | AAT | 5 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(2): Show |
5 | HG00280.hp1 HG01074.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.1415+1166_1415+116 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585048 | |||||||
| chr11:110585068 | CATATATG others(11): Show |
C | 1 | a0001c0001t0002g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1415+1130_1415+114 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585068 | |||||||
| chr11:110585080 | CATGAATA others(11): Show |
C | 1 | a0001c0002t0005g0212 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1415+1118_1415+113 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585080 | |||||||
| chr11:110585095 | AT | A | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1415+1120delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585095 | |||||||
| chr11:110585227 | G | A | 27 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(24): Show |
28 | HG00280.hp2 HG00733.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.1415+989C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585227 | |||||||
| chr11:110585228 | A | T | 5 | a0002c0003t0007g0148 a0002c0003t0007g0199 a0002c0003t0007g0203 others(2): Show |
5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1415+988T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585228 | |||||||
| chr11:110585286 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1415+930A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585286 | |||||||
| chr11:110585378 | T | C | 5 | a0002c0003t0007g0148 a0002c0003t0007g0199 a0002c0003t0007g0203 others(2): Show |
5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1415+838A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585378 | |||||||
| chr11:110585408 | C | CCTTGGTT others(13): Show |
4 | a0003c0004t0002g0142 a0003c0004t0002g0160 a0003c0004t0017g0143 others(1): Show |
4 | HG03491.hp1 HG03688.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1415+788_1415+807d others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585408 | |||||||
| chr11:110585496 | A | G | 8 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(5): Show |
9 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1415+720T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585496 | |||||||
| chr11:110585529 | A | G | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0019 others(76): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.1415+687T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585529 | |||||||
| chr11:110585579 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1415+637T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585579 | |||||||
| chr11:110585649 | C | T | 2 | a0011c0015t0004g0151 a0013c0019t0004g0149 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1415+567G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585649 | |||||||
| chr11:110585726 | C | G | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1415+490G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585726 | |||||||
| chr11:110585914 | G | A | 5 | a0002c0003t0007g0148 a0002c0003t0007g0199 a0002c0003t0007g0203 others(2): Show |
5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1415+302C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | 110585914 | |||||||
| chr11:110586484 | GA | G | 5 | a0002c0003t0007g0148 a0002c0003t0007g0199 a0002c0003t0007g0203 others(2): Show |
5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306-160delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110586484 | |||||||
| chr11:110586611 | T | A | 2 | a0001c0005t0005g0140 a0001c0005t0005g0194 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1306-286A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110586611 | |||||||
| chr11:110586650 | C | T | 1 | a0001c0002t0005g0212 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1306-325G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110586650 | |||||||
| chr11:110586748 | C | A | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1306-423G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110586748 | |||||||
| chr11:110586776 | T | C | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1306-451A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110586776 | |||||||
| chr11:110586920 | GGA | G | 12 | a0001c0002t0005g0113 a0001c0002t0005g0206 a0001c0002t0005g0208 others(9): Show |
12 | HG00280.hp2 HG00733.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1306-597_1306-596d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110586920 | |||||||
| chr11:110587086 | C | CACAA | 3 | a0003c0004t0002g0142 a0003c0004t0002g0160 a0012c0017t0002g0139 |
3 | HG03491.hp1 HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.1306-765_1306-762d others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110587086 | |||||||
| chr11:110587461 | C | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0019 others(156): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1306-1136G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110587461 | |||||||
| chr11:110587535 | G | T | 3 | a0002c0006t0012g0111 a0002c0006t0012g0138 a0002c0014t0019g0204 |
3 | HG01952.hp2 HG02055.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1306-1210C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110587535 | |||||||
| chr11:110587577 | C | T | 2 | a0011c0015t0004g0151 a0013c0019t0004g0149 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1306-1252G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110587577 | |||||||
| chr11:110587660 | T | C | 1 | a0001c0001t0003g0087 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1306-1335A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110587660 | |||||||
| chr11:110587763 | C | CT | 53 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0005 others(50): Show |
57 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.1306-1439dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110587763 | |||||||
| chr11:110587893 | C | A | 5 | a0002c0003t0007g0148 a0002c0003t0007g0199 a0002c0003t0007g0203 others(2): Show |
5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306-1568G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110587893 | |||||||
| chr11:110587910 | T | A | 5 | a0002c0003t0007g0148 a0002c0003t0007g0199 a0002c0003t0007g0203 others(2): Show |
5 | HG02257.hp1 HG02723.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306-1585A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110587910 | |||||||
| chr11:110587912 | G | T | 1 | a0001c0001t0001g0097 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1306-1587C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110587912 | |||||||
| chr11:110588111 | G | A | 33 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0039 others(30): Show |
36 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(33): Show |
intron_variant | MODIFIER | c.1306-1786C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588111 | |||||||
| chr11:110588162 | C | A | 214 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0019 others(211): Show |
223 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(220): Show |
intron_variant | MODIFIER | c.1306-1837G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588162 | |||||||
| chr11:110588167 | T | C | 8 | a0001c0001t0002g0093 a0001c0001t0002g0156 a0001c0001t0002g0157 others(5): Show |
8 | HG00673.hp2 HG02040.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1306-1842A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588167 | |||||||
| chr11:110588196 | G | T | 3 | a0002c0003t0007g0199 a0002c0003t0007g0203 a0002c0003t0007g0205 |
3 | HG02723.hp1 HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1306-1871C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588196 | |||||||
| chr11:110588237 | T | C | 3 | a0001c0001t0006g0196 a0001c0001t0006g0197 a0001c0001t0006g0198 |
3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1306-1912A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588237 | |||||||
| chr11:110588264 | A | C | 2 | a0011c0015t0004g0151 a0013c0019t0004g0149 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1306-1939T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588264 | |||||||
| chr11:110588336 | C | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0019 others(75): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1306-2011G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588336 | |||||||
| chr11:110588419 | T | C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0019 others(76): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.1306-2094A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588419 | |||||||
| chr11:110588511 | A | G | 1 | a0001c0001t0003g0015 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1305+2137T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588511 | |||||||
| chr11:110588868 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1305+1780C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588868 | |||||||
| chr11:110588898 | C | T | 1 | a0001c0002t0005g0208 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1305+1750G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588898 | |||||||
| chr11:110588931 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1305+1717C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110588931 | |||||||
| chr11:110589026 | C | T | 44 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0005 others(41): Show |
48 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.1305+1622G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110589026 | |||||||
| chr11:110589058 | T | C | 135 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0019 others(132): Show |
143 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1305+1590A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110589058 | |||||||
| chr11:110589067 | G | A | 44 | a0001c0001t0003g0001 a0001c0001t0003g0003 a0001c0001t0003g0005 others(41): Show |
48 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.1305+1581C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110589067 | |||||||
| chr11:110589108 | T | C | 1 | a0001c0001t0002g0125 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1305+1540A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110589108 | |||||||
| chr11:110589143 | T | C | 3 | a0002c0006t0012g0111 a0002c0006t0012g0138 a0002c0014t0019g0204 |
3 | HG01952.hp2 HG02055.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1305+1505A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110589143 | |||||||
| chr11:110589355 | G | A | 1 | a0001c0001t0003g0102 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1305+1293C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110589355 | |||||||
| chr11:110589653 | T | C | 3 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0044 |
3 | NA18940.hp2 NA18978.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1305+995A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110589653 | |||||||
| chr11:110589817 | A | G | 1 | a0013c0019t0004g0149 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1305+831T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110589817 | |||||||
| chr11:110590042 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1305+606T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110590042 | |||||||
| chr11:110590116 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1305+532C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110590116 | |||||||
| chr11:110590120 | C | CA | 17 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0168 others(14): Show |
17 | HG00323.hp1 HG00735.hp2 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.1305+527dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110590120 | |||||||
| chr11:110590120 | CA | C | 14 | a0001c0001t0002g0098 a0001c0001t0002g0120 a0001c0002t0005g0113 others(11): Show |
14 | HG00280.hp2 HG00733.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1305+527delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 11/14 | chr11 | 110590120 | |||||||
| chr11:110590820 | G | A | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1144-11C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/14 | chr11 | 110590820 | |||||||
| chr11:110590865 | T | C | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1144-56A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/14 | chr11 | 110590865 | |||||||
| chr11:110590903 | C | T | 1 | a0001c0001t0002g0024 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1144-94G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/14 | chr11 | 110590903 | |||||||
| chr11:110590947 | G | A | 2 | a0001c0001t0003g0001 a0001c0001t0003g0051 |
4 | HG01928.hp2 HG01981.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1144-138C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/14 | chr11 | 110590947 | |||||||
| chr11:110591224 | C | A | 2 | a0011c0015t0004g0151 a0013c0019t0004g0149 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1144-415G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/14 | chr11 | 110591224 | |||||||
| chr11:110591540 | T | C | 1 | a0001c0001t0002g0074 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1143+437A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/14 | chr11 | 110591540 | |||||||
| chr11:110591582 | G | A | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1143+395C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/14 | chr11 | 110591582 | |||||||
| chr11:110591762 | G | A | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1143+215C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/14 | chr11 | 110591762 | |||||||
| chr11:110591791 | T | C | 8 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(5): Show |
9 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1143+186A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 10/14 | chr11 | 110591791 | |||||||
| chr11:110592262 | G | C | 51 | a0001c0001t0001g0130 a0001c0001t0003g0001 a0001c0001t0003g0003 others(48): Show |
55 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.965-107C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110592262 | |||||||
| chr11:110592370 | G | T | 1 | a0001c0001t0002g0035 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.965-215C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110592370 | |||||||
| chr11:110592375 | T | C | 4 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-220A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110592375 | |||||||
| chr11:110592825 | T | C | 1 | a0001c0001t0003g0104 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.965-670A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110592825 | |||||||
| chr11:110593045 | T | C | 3 | a0002c0006t0012g0138 a0002c0014t0019g0204 a0003c0004t0017g0143 |
3 | HG01952.hp2 HG03017.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.965-890A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110593045 | |||||||
| chr11:110593270 | C | T | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.965-1115G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110593270 | |||||||
| chr11:110593510 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.965-1355A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110593510 | |||||||
| chr11:110593647 | A | G | 1 | a0002c0003t0007g0199 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.965-1492T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110593647 | |||||||
| chr11:110593904 | T | G | 129 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(126): Show |
134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.965-1749A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110593904 | |||||||
| chr11:110593976 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.965-1821A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110593976 | |||||||
| chr11:110594300 | C | A | 8 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(5): Show |
9 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.965-2145G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594300 | |||||||
| chr11:110594327 | C | T | 26 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0004g0006 others(23): Show |
27 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.965-2172G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594327 | |||||||
| chr11:110594493 | A | G | 4 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-2338T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594493 | |||||||
| chr11:110594587 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.965-2432G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594587 | |||||||
| chr11:110594668 | G | C | 4 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-2513C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594668 | |||||||
| chr11:110594805 | C | G | 2 | a0001c0001t0003g0005 a0001c0001t0003g0124 |
3 | NA18942.hp2 NA18948.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.965-2650G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594805 | |||||||
| chr11:110594819 | T | G | 1 | a0001c0001t0001g0150 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.965-2664A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594819 | |||||||
| chr11:110594833 | CA | C | 75 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0024 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.965-2679delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594833 | |||||||
| chr11:110594951 | C | A | 128 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(125): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.965-2796G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594951 | |||||||
| chr11:110594992 | C | T | 48 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0003g0001 others(45): Show |
53 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.965-2837G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110594992 | |||||||
| chr11:110595137 | C | T | 27 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0004g0006 others(24): Show |
28 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.965-2982G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595137 | |||||||
| chr11:110595208 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.965-3053C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595208 | |||||||
| chr11:110595217 | A | C | 1 | a0001c0001t0002g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.965-3062T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595217 | |||||||
| chr11:110595533 | C | A | 1 | a0001c0001t0001g0058 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.965-3378G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595533 | |||||||
| chr11:110595544 | T | C | 1 | a0001c0001t0003g0083 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.965-3389A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595544 | |||||||
| chr11:110595614 | C | T | 7 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(4): Show |
8 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.965-3459G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595614 | |||||||
| chr11:110595730 | A | G | 42 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0003g0001 others(39): Show |
46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.965-3575T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595730 | |||||||
| chr11:110595752 | C | G | 3 | a0001c0001t0001g0127 a0001c0008t0003g0099 a0001c0008t0003g0100 |
3 | NA19000.hp2 NA19003.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.965-3597G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595752 | |||||||
| chr11:110595874 | C | T | 2 | a0003c0004t0002g0142 a0012c0017t0002g0139 |
2 | HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.965-3719G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595874 | |||||||
| chr11:110595899 | C | T | 1 | a0002c0006t0012g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.965-3744G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595899 | |||||||
| chr11:110595923 | A | G | 1 | a0002c0006t0012g0138 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.965-3768T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595923 | |||||||
| chr11:110595976 | T | C | 79 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0024 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.965-3821A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595976 | |||||||
| chr11:110595989 | A | G | 128 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(125): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.965-3834T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110595989 | |||||||
| chr11:110596025 | C | G | 9 | a0001c0001t0002g0028 a0001c0001t0002g0031 a0001c0001t0002g0033 others(6): Show |
9 | HG01109.hp2 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.965-3870G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596025 | |||||||
| chr11:110596035 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.965-3880G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596035 | |||||||
| chr11:110596070 | C | T | 26 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0004g0006 others(23): Show |
27 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.965-3915G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596070 | |||||||
| chr11:110596076 | A | G | 49 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0200 others(46): Show |
53 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.965-3921T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596076 | |||||||
| chr11:110596239 | G | A | 1 | a0001c0002t0005g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.965-4084C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596239 | |||||||
| chr11:110596273 | CA | C | 45 | a0001c0001t0002g0010 a0001c0001t0002g0024 a0001c0001t0002g0025 others(42): Show |
45 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.965-4119delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596273 | |||||||
| chr11:110596276 | G | A | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.965-4121C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596276 | |||||||
| chr11:110596277 | G | A | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.965-4122C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596277 | |||||||
| chr11:110596310 | A | G | 122 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(119): Show |
127 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.965-4155T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596310 | |||||||
| chr11:110596313 | G | A | 2 | a0003c0004t0002g0142 a0012c0017t0002g0139 |
2 | HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.965-4158C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596313 | |||||||
| chr11:110596365 | A | G | 124 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(121): Show |
129 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.965-4210T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596365 | |||||||
| chr11:110596376 | C | A | 1 | a0001c0001t0001g0027 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.965-4221G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596376 | |||||||
| chr11:110596387 | C | T | 47 | a0001c0001t0002g0010 a0001c0001t0002g0024 a0001c0001t0002g0025 others(44): Show |
47 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.965-4232G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596387 | |||||||
| chr11:110596426 | G | A | 128 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(125): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.965-4271C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596426 | |||||||
| chr11:110596427 | T | A | 4 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.965-4272A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596427 | |||||||
| chr11:110596438 | G | A | 128 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(125): Show |
133 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.965-4283C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596438 | |||||||
| chr11:110596477 | A | G | 10 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.965-4322T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596477 | |||||||
| chr11:110596556 | C | G | 9 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
9 | HG01981.hp1 HG02040.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.965-4401G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596556 | |||||||
| chr11:110596615 | G | A | 2 | a0002c0006t0012g0138 a0002c0014t0019g0204 |
2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.965-4460C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596615 | |||||||
| chr11:110596668 | C | T | 25 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0004g0006 others(22): Show |
26 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.965-4513G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596668 | |||||||
| chr11:110596729 | A | G | 129 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(126): Show |
134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.965-4574T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596729 | |||||||
| chr11:110596734 | G | A | 26 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0004g0006 others(23): Show |
27 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.965-4579C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596734 | |||||||
| chr11:110596825 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0170 |
2 | HG01169.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.965-4670A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596825 | |||||||
| chr11:110596904 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0137 |
2 | HG00735.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.965-4749C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596904 | |||||||
| chr11:110596975 | GTTCAT | G | 3 | a0007c0018t0015g0009 a0011c0015t0004g0151 a0013c0019t0004g0149 |
3 | HG02809.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.965-4825_965-4821d others(7): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110596975 | |||||||
| chr11:110597035 | G | A | 5 | a0001c0001t0001g0184 a0001c0001t0002g0045 a0001c0001t0003g0015 others(2): Show |
5 | HG01261.hp2 HG01433.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-4880C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597035 | |||||||
| chr11:110597056 | C | T | 48 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0200 others(45): Show |
52 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.965-4901G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597056 | |||||||
| chr11:110597136 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.965-4981C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597136 | |||||||
| chr11:110597139 | G | T | 1 | a0001c0001t0001g0060 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.965-4984C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597139 | |||||||
| chr11:110597145 | T | TG | 8 | a0001c0001t0001g0091 a0001c0001t0001g0131 a0001c0001t0002g0074 others(5): Show |
8 | HG02602.hp2 HG03017.hp2 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.965-4991dupC | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597145 | |||||||
| chr11:110597294 | T | TA | 19 | a0001c0001t0001g0207 a0001c0001t0003g0104 a0001c0001t0003g0209 others(16): Show |
19 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.965-5140dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597294 | |||||||
| chr11:110597294 | T | TAA | 45 | a0001c0001t0002g0010 a0001c0001t0002g0024 a0001c0001t0002g0025 others(42): Show |
45 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.965-5141_965-5140d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597294 | |||||||
| chr11:110597294 | TA | T | 5 | a0001c0001t0003g0023 a0001c0001t0003g0086 a0001c0001t0003g0087 others(2): Show |
5 | HG03834.hp2 HG03942.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.965-5140delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597294 | |||||||
| chr11:110597394 | T | C | 1 | a0001c0001t0003g0040 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.965-5239A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597394 | |||||||
| chr11:110597471 | T | C | 1 | a0011c0015t0004g0151 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.965-5316A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597471 | |||||||
| chr11:110597565 | T | C | 7 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(4): Show |
8 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.965-5410A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110597565 | |||||||
| chr11:110598137 | G | A | 2 | a0001c0001t0003g0067 a0001c0001t0003g0121 |
2 | HG02683.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.965-5982C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110598137 | |||||||
| chr11:110598172 | C | CT | 121 | a0001c0001t0001g0114 a0001c0001t0001g0130 a0001c0001t0001g0161 others(118): Show |
126 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.965-6018dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110598172 | |||||||
| chr11:110598185 | T | TC | 4 | a0001c0005t0005g0140 a0001c0005t0005g0194 a0003c0004t0002g0142 others(1): Show |
4 | HG01891.hp1 HG02451.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.965-6031dupG | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110598185 | |||||||
| chr11:110598602 | A | G | 75 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0024 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.965-6447T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110598602 | |||||||
| chr11:110598744 | T | C | 1 | a0002c0003t0007g0148 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.965-6589A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110598744 | |||||||
| chr11:110598773 | G | A | 75 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0024 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.965-6618C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110598773 | |||||||
| chr11:110598886 | G | A | 1 | a0002c0006t0012g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.965-6731C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110598886 | |||||||
| chr11:110598901 | C | T | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.965-6746G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110598901 | |||||||
| chr11:110599182 | A | G | 1 | a0001c0001t0003g0083 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.965-7027T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599182 | |||||||
| chr11:110599231 | C | G | 3 | a0001c0001t0006g0196 a0001c0001t0006g0197 a0001c0001t0006g0198 |
3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.965-7076G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599231 | |||||||
| chr11:110599386 | C | A | 23 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0004g0006 others(20): Show |
24 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.964+7175G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599386 | |||||||
| chr11:110599402 | AC | A | 4 | a0001c0001t0002g0010 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+7158delG | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599402 | |||||||
| chr11:110599425 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.964+7136C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599425 | |||||||
| chr11:110599434 | C | T | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.964+7127G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599434 | |||||||
| chr11:110599456 | G | T | 1 | a0001c0001t0001g0022 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.964+7105C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599456 | |||||||
| chr11:110599498 | G | A | 1 | a0001c0001t0003g0003 | 2 | NA18951.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.964+7063C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599498 | |||||||
| chr11:110599766 | GACTACCC | G | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.964+6788_964+6794d others(9): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599766 | |||||||
| chr11:110599831 | G | A | 2 | a0002c0006t0012g0138 a0002c0014t0019g0204 |
2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.964+6730C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599831 | |||||||
| chr11:110599862 | C | G | 127 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(124): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.964+6699G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599862 | |||||||
| chr11:110599867 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG01261.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.964+6694G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599867 | |||||||
| chr11:110599915 | G | T | 4 | a0001c0001t0003g0209 a0001c0002t0005g0208 a0001c0002t0005g0214 others(1): Show |
4 | HG02015.hp1 HG02080.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+6646C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110599915 | |||||||
| chr11:110600088 | C | G | 2 | a0003c0004t0002g0142 a0012c0017t0002g0139 |
2 | HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.964+6473G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600088 | |||||||
| chr11:110600190 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.964+6371C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600190 | |||||||
| chr11:110600235 | T | G | 2 | a0001c0001t0003g0092 a0001c0001t0003g0102 |
2 | HG01346.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.964+6326A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600235 | |||||||
| chr11:110600327 | T | C | 4 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+6234A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600327 | |||||||
| chr11:110600404 | A | C | 47 | a0001c0001t0002g0010 a0001c0001t0002g0024 a0001c0001t0002g0025 others(44): Show |
47 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.964+6157T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600404 | |||||||
| chr11:110600443 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.964+6118G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600443 | |||||||
| chr11:110600510 | G | A | 1 | a0003c0004t0002g0160 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.964+6051C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600510 | |||||||
| chr11:110600514 | C | A | 30 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0004g0006 others(27): Show |
31 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.964+6047G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600514 | |||||||
| chr11:110600588 | T | G | 79 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0024 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.964+5973A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600588 | |||||||
| chr11:110600700 | ATAACAGT others(12): Show |
A | 10 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.964+5842_964+5860d others(21): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600700 | |||||||
| chr11:110600753 | G | T | 1 | a0004c0010t0001g0179 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.964+5808C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600753 | |||||||
| chr11:110600812 | GA | G | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.964+5748delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110600812 | |||||||
| chr11:110601107 | G | A | 2 | a0002c0006t0012g0138 a0002c0014t0019g0204 |
2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.964+5454C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601107 | |||||||
| chr11:110601306 | T | C | 41 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0003g0001 others(38): Show |
45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.964+5255A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601306 | |||||||
| chr11:110601444 | A | G | 13 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(10): Show |
13 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.964+5117T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601444 | |||||||
| chr11:110601763 | C | A | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.964+4798G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601763 | |||||||
| chr11:110601829 | C | CA | 7 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(4): Show |
8 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.964+4731dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601829 | |||||||
| chr11:110601835 | A | T | 1 | a0001c0001t0003g0085 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.964+4726T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601835 | |||||||
| chr11:110601837 | A | G | 45 | a0001c0001t0002g0010 a0001c0001t0002g0024 a0001c0001t0002g0025 others(42): Show |
45 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.964+4724T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601837 | |||||||
| chr11:110601898 | GA | G | 4 | a0001c0001t0001g0049 a0001c0001t0001g0073 a0001c0001t0001g0097 others(1): Show |
4 | HG01928.hp1 NA18948.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+4662delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601898 | |||||||
| chr11:110601981 | C | CA | 14 | a0001c0001t0001g0131 a0001c0001t0002g0200 a0001c0001t0002g0201 others(11): Show |
14 | HG01074.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.964+4579dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601981 | |||||||
| chr11:110601981 | CA | C | 67 | a0001c0001t0001g0082 a0001c0001t0001g0088 a0001c0001t0001g0106 others(64): Show |
67 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.964+4579delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601981 | |||||||
| chr11:110601998 | A | T | 1 | a0002c0014t0019g0204 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.964+4563T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110601998 | |||||||
| chr11:110602112 | T | A | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.964+4449A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110602112 | |||||||
| chr11:110602214 | C | T | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.964+4347G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110602214 | |||||||
| chr11:110602222 | C | CT | 121 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(118): Show |
126 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.964+4338dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110602222 | |||||||
| chr11:110602399 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.964+4162A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110602399 | |||||||
| chr11:110602513 | T | C | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.964+4048A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110602513 | |||||||
| chr11:110602999 | G | C | 75 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0024 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.964+3562C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110602999 | |||||||
| chr11:110603251 | T | C | 2 | a0001c0005t0005g0140 a0001c0005t0005g0194 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.964+3310A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110603251 | |||||||
| chr11:110603359 | A | G | 7 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(4): Show |
8 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.964+3202T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110603359 | |||||||
| chr11:110603555 | T | A | 4 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.964+3006A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110603555 | |||||||
| chr11:110603574 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0170 |
2 | HG01169.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.964+2987A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110603574 | |||||||
| chr11:110603803 | C | A | 41 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0003g0001 others(38): Show |
45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.964+2758G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110603803 | |||||||
| chr11:110604064 | T | C | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.964+2497A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110604064 | |||||||
| chr11:110604250 | G | A | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.964+2311C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110604250 | |||||||
| chr11:110604271 | C | T | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.964+2290G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110604271 | |||||||
| chr11:110604585 | T | C | 13 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(10): Show |
13 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.964+1976A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110604585 | |||||||
| chr11:110604684 | A | G | 75 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0024 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.964+1877T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110604684 | |||||||
| chr11:110604761 | G | A | 75 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0024 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.964+1800C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110604761 | |||||||
| chr11:110604766 | T | C | 30 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0004g0006 others(27): Show |
31 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.964+1795A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110604766 | |||||||
| chr11:110604814 | C | G | 2 | a0006c0011t0002g0030 a0006c0011t0002g0126 |
2 | NA19075.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.964+1747G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110604814 | |||||||
| chr11:110604996 | A | G | 2 | a0003c0004t0002g0142 a0012c0017t0002g0139 |
2 | HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.964+1565T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110604996 | |||||||
| chr11:110605010 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.964+1551C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605010 | |||||||
| chr11:110605176 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.964+1385A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605176 | |||||||
| chr11:110605202 | T | A | 2 | a0001c0001t0002g0201 a0001c0001t0002g0202 |
2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.964+1359A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605202 | |||||||
| chr11:110605335 | T | C | 49 | a0001c0001t0002g0010 a0001c0001t0002g0024 a0001c0001t0002g0025 others(46): Show |
49 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.964+1226A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605335 | |||||||
| chr11:110605516 | G | A | 3 | a0007c0018t0015g0009 a0011c0015t0004g0151 a0013c0019t0004g0149 |
3 | HG02809.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.964+1045C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605516 | |||||||
| chr11:110605724 | T | G | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 |
3 | HG00280.hp1 HG01074.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.964+837A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605724 | |||||||
| chr11:110605812 | C | T | 47 | a0001c0001t0002g0010 a0001c0001t0002g0024 a0001c0001t0002g0025 others(44): Show |
47 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(44): Show |
intron_variant | MODIFIER | c.964+749G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605812 | |||||||
| chr11:110605822 | C | G | 41 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0003g0001 others(38): Show |
45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.964+739G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605822 | |||||||
| chr11:110605823 | G | A | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.964+738C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605823 | |||||||
| chr11:110605870 | T | C | 1 | a0002c0006t0012g0138 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.964+691A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605870 | |||||||
| chr11:110605907 | AC | A | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.964+653delG | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605907 | |||||||
| chr11:110605961 | G | A | 41 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0003g0001 others(38): Show |
45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.964+600C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110605961 | |||||||
| chr11:110606148 | A | G | 2 | a0002c0006t0012g0138 a0002c0014t0019g0204 |
2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.964+413T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110606148 | |||||||
| chr11:110606167 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.964+394T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110606167 | |||||||
| chr11:110606191 | T | C | 1 | a0001c0001t0011g0018 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.964+370A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110606191 | |||||||
| chr11:110606202 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.964+359G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110606202 | |||||||
| chr11:110606309 | T | C | 1 | a0002c0014t0019g0204 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.964+252A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110606309 | |||||||
| chr11:110606488 | C | A | 36 | a0001c0001t0002g0026 a0001c0001t0002g0028 a0001c0001t0002g0031 others(33): Show |
36 | HG00558.hp2 HG01109.hp2 HG01192.hp2 others(33): Show |
intron_variant | MODIFIER | c.964+73G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110606488 | |||||||
| chr11:110606546 | C | T | 1 | a0001c0001t0003g0067 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.964+15G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 9/14 | chr11 | 110606546 | |||||||
| chr11:110607075 | T | C | 23 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0004g0006 others(20): Show |
24 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.776-326A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110607075 | |||||||
| chr11:110607183 | A | G | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.776-434T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110607183 | |||||||
| chr11:110607484 | G | A | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.776-735C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110607484 | |||||||
| chr11:110607673 | A | G | 1 | a0001c0001t0006g0154 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.776-924T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110607673 | |||||||
| chr11:110607816 | A | G | 1 | a0002c0006t0012g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.776-1067T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110607816 | |||||||
| chr11:110607868 | A | G | 50 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(47): Show |
51 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.775+1116T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110607868 | |||||||
| chr11:110607929 | A | C | 1 | a0011c0015t0004g0151 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.775+1055T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110607929 | |||||||
| chr11:110607998 | C | T | 79 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0024 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.775+986G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110607998 | |||||||
| chr11:110608147 | A | T | 49 | a0001c0001t0002g0010 a0001c0001t0002g0024 a0001c0001t0002g0025 others(46): Show |
49 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.775+837T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110608147 | |||||||
| chr11:110608839 | T | C | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.775+145A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 8/14 | chr11 | 110608839 | |||||||
| chr11:110609072 | T | C | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.709-22A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110609072 | |||||||
| chr11:110609115 | A | ATT | 23 | a0001c0001t0001g0207 a0001c0001t0002g0026 a0001c0001t0003g0209 others(20): Show |
24 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.709-67_709-66dupAA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110609115 | |||||||
| chr11:110609115 | ATTT | A | 41 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0003g0001 others(38): Show |
45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.709-68_709-66delAA others(1): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110609115 | |||||||
| chr11:110609120 | T | A | 4 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.709-70A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110609120 | |||||||
| chr11:110609305 | T | C | 1 | a0001c0001t0002g0200 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.709-255A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110609305 | |||||||
| chr11:110609681 | T | C | 8 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(5): Show |
9 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.709-631A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110609681 | |||||||
| chr11:110609692 | C | A | 4 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.709-642G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110609692 | |||||||
| chr11:110609797 | T | C | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.709-747A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110609797 | |||||||
| chr11:110609833 | C | T | 2 | a0003c0004t0002g0142 a0012c0017t0002g0139 |
2 | HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.709-783G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110609833 | |||||||
| chr11:110610051 | A | T | 2 | a0002c0006t0012g0138 a0002c0014t0019g0204 |
2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.709-1001T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610051 | |||||||
| chr11:110610082 | A | T | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.709-1032T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610082 | |||||||
| chr11:110610310 | C | CAATT | 129 | a0001c0001t0001g0039 a0001c0001t0001g0130 a0001c0001t0001g0161 others(126): Show |
134 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.708+998_708+999ins others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610310 | |||||||
| chr11:110610326 | T | C | 3 | a0001c0001t0003g0023 a0001c0001t0003g0086 a0001c0001t0003g0087 |
3 | NA18954.hp1 NA18999.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.708+983A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610326 | |||||||
| chr11:110610391 | T | A | 1 | a0001c0001t0001g0155 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.708+918A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610391 | |||||||
| chr11:110610430 | T | A | 2 | a0002c0006t0012g0138 a0002c0014t0019g0204 |
2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.708+879A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610430 | |||||||
| chr11:110610431 | G | T | 2 | a0002c0006t0012g0138 a0002c0014t0019g0204 |
2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.708+878C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610431 | |||||||
| chr11:110610554 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.708+755A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610554 | |||||||
| chr11:110610647 | C | G | 1 | a0013c0019t0004g0149 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.708+662G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610647 | |||||||
| chr11:110610658 | C | G | 2 | a0003c0004t0002g0142 a0012c0017t0002g0139 |
2 | HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.708+651G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610658 | |||||||
| chr11:110610659 | T | C | 1 | a0001c0001t0002g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.708+650A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110610659 | |||||||
| chr11:110611032 | A | G | 16 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0006g0154 others(13): Show |
16 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.708+277T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 7/14 | chr11 | 110611032 | |||||||
| chr11:110611420 | A | G | 4 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0002c0003t0007g0203 others(1): Show |
4 | HG01891.hp2 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.631-34T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110611420 | |||||||
| chr11:110611470 | G | A | 2 | a0011c0015t0004g0151 a0013c0019t0004g0149 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.631-84C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110611470 | |||||||
| chr11:110611505 | C | A | 77 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(74): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.631-119G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110611505 | |||||||
| chr11:110611574 | C | T | 1 | a0001c0002t0005g0208 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.631-188G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110611574 | |||||||
| chr11:110611602 | T | C | 1 | a0002c0006t0012g0138 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.631-216A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110611602 | |||||||
| chr11:110611748 | G | A | 2 | a0001c0005t0005g0140 a0001c0005t0005g0194 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.631-362C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110611748 | |||||||
| chr11:110611789 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.631-403T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110611789 | |||||||
| chr11:110611818 | C | CAGG | 77 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(74): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.631-433_631-432ins others(3): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110611818 | |||||||
| chr11:110612137 | A | T | 4 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.631-751T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612137 | |||||||
| chr11:110612214 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.631-828G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612214 | |||||||
| chr11:110612254 | T | TAA | 51 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(48): Show |
52 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.631-870_631-869dup others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612254 | |||||||
| chr11:110612317 | A | G | 6 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(3): Show |
6 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.631-931T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612317 | |||||||
| chr11:110612347 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.631-961C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612347 | |||||||
| chr11:110612357 | G | A | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.631-971C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612357 | |||||||
| chr11:110612560 | C | T | 2 | a0001c0008t0003g0099 a0001c0008t0003g0100 |
2 | NA19000.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.631-1174G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612560 | |||||||
| chr11:110612875 | G | A | 42 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(39): Show |
46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.631-1489C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612875 | |||||||
| chr11:110612899 | C | T | 48 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(45): Show |
52 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.631-1513G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612899 | |||||||
| chr11:110612916 | C | T | 1 | a0012c0017t0002g0139 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.631-1530G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612916 | |||||||
| chr11:110612983 | C | T | 2 | a0001c0005t0005g0140 a0001c0005t0005g0194 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.630+1578G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110612983 | |||||||
| chr11:110613040 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0172 a0001c0001t0001g0190 |
4 | HG02622.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+1521A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110613040 | |||||||
| chr11:110613421 | C | T | 1 | a0001c0001t0004g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.630+1140G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110613421 | |||||||
| chr11:110613529 | T | G | 19 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0006g0154 others(16): Show |
19 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.630+1032A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110613529 | |||||||
| chr11:110613697 | A | G | 2 | a0001c0001t0006g0197 a0001c0001t0006g0198 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.630+864T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110613697 | |||||||
| chr11:110613827 | C | A | 50 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(47): Show |
51 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.630+734G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110613827 | |||||||
| chr11:110613883 | T | C | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.630+678A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110613883 | |||||||
| chr11:110614038 | C | T | 1 | a0001c0001t0006g0154 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.630+523G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110614038 | |||||||
| chr11:110614175 | TTAA | T | 10 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(7): Show |
11 | HG01891.hp1 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.630+383_630+385del others(3): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110614175 | |||||||
| chr11:110614266 | A | G | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.630+295T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110614266 | |||||||
| chr11:110614417 | C | T | 4 | a0002c0003t0007g0148 a0007c0018t0015g0009 a0011c0015t0004g0151 others(1): Show |
4 | HG02257.hp1 HG02809.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+144G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110614417 | |||||||
| chr11:110614466 | A | AGCCT | 6 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(3): Show |
6 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.630+91_630+94dupAG others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110614466 | |||||||
| chr11:110614502 | G | A | 1 | a0002c0003t0007g0199 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.630+59C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110614502 | |||||||
| chr11:110614508 | T | C | 1 | a0001c0001t0003g0051 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.630+53A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 6/14 | chr11 | 110614508 | |||||||
| chr11:110614660 | C | T | 2 | a0001c0005t0005g0140 a0001c0005t0005g0194 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.546-15G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 5/14 | chr11 | 110614660 | |||||||
| chr11:110614670 | A | G | 1 | a0001c0001t0001g0027 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.546-25T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 5/14 | chr11 | 110614670 | |||||||
| chr11:110614771 | T | C | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.546-126A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 5/14 | chr11 | 110614771 | |||||||
| chr11:110615019 | A | T | 7 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(4): Show |
8 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.546-374T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 5/14 | chr11 | 110615019 | |||||||
| chr11:110615279 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.545+274C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 5/14 | chr11 | 110615279 | |||||||
| chr11:110615327 | C | T | 1 | a0002c0006t0012g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.545+226G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 5/14 | chr11 | 110615327 | |||||||
| chr11:110615396 | G | C | 45 | a0001c0001t0001g0039 a0001c0001t0002g0010 a0001c0001t0002g0024 others(42): Show |
45 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(42): Show |
intron_variant | MODIFIER | c.545+157C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 5/14 | chr11 | 110615396 | |||||||
| chr11:110615746 | C | G | 29 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0004g0006 others(26): Show |
30 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.504-152G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110615746 | |||||||
| chr11:110615892 | T | A | 1 | a0002c0006t0012g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.504-298A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110615892 | |||||||
| chr11:110616096 | G | C | 1 | a0001c0002t0005g0214 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.504-502C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110616096 | |||||||
| chr11:110616155 | T | TA | 41 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(38): Show |
45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.504-562dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110616155 | |||||||
| chr11:110616427 | T | C | 46 | a0001c0001t0001g0039 a0001c0001t0002g0010 a0001c0001t0002g0024 others(43): Show |
46 | HG00558.hp2 HG00738.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.504-833A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110616427 | |||||||
| chr11:110616507 | A | G | 81 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(78): Show |
86 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.504-913T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110616507 | |||||||
| chr11:110616686 | C | CT | 57 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(54): Show |
61 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.504-1093dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110616686 | |||||||
| chr11:110616686 | C | T | 1 | a0001c0001t0003g0133 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.504-1092G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110616686 | |||||||
| chr11:110616686 | CT | C | 17 | a0001c0001t0001g0191 a0001c0001t0004g0006 a0001c0001t0004g0011 others(14): Show |
18 | HG01952.hp2 HG02145.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.504-1093delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110616686 | |||||||
| chr11:110617120 | G | A | 1 | a0001c0002t0005g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.504-1526C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110617120 | |||||||
| chr11:110617419 | C | T | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.504-1825G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110617419 | |||||||
| chr11:110617515 | C | G | 81 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(78): Show |
86 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.504-1921G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110617515 | |||||||
| chr11:110617824 | C | A | 2 | a0002c0006t0012g0138 a0002c0014t0019g0204 |
2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.504-2230G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110617824 | |||||||
| chr11:110617891 | C | T | 3 | a0001c0001t0006g0196 a0001c0001t0006g0197 a0001c0001t0006g0198 |
3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.504-2297G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110617891 | |||||||
| chr11:110618161 | G | GA | 28 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0004g0006 others(25): Show |
29 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.504-2568dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618161 | |||||||
| chr11:110618161 | G | GAAAAAAA others(13): Show |
1 | a0001c0002t0005g0213 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.504-2568_504-2567i others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618161 | |||||||
| chr11:110618190 | A | G | 29 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0004g0006 others(26): Show |
30 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.504-2596T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618190 | |||||||
| chr11:110618291 | C | G | 2 | a0003c0004t0002g0142 a0012c0017t0002g0139 |
2 | HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.504-2697G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618291 | |||||||
| chr11:110618449 | G | T | 83 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(80): Show |
88 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.504-2855C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618449 | |||||||
| chr11:110618491 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.504-2897G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618491 | |||||||
| chr11:110618501 | G | A | 2 | a0011c0015t0004g0151 a0013c0019t0004g0149 |
2 | NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.504-2907C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618501 | |||||||
| chr11:110618543 | T | C | 1 | a0001c0002t0005g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.504-2949A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618543 | |||||||
| chr11:110618546 | G | A | 1 | a0001c0002t0005g0211 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.504-2952C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618546 | |||||||
| chr11:110618581 | TAGTGATA others(10): Show |
T | 4 | a0002c0006t0012g0138 a0002c0014t0019g0204 a0005c0007t0010g0145 others(1): Show |
4 | HG01952.hp2 HG02622.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.504-3004_504-2988d others(19): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618581 | |||||||
| chr11:110618655 | T | C | 2 | a0003c0004t0002g0142 a0012c0017t0002g0139 |
2 | HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.504-3061A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618655 | |||||||
| chr11:110618671 | ATAGAGTA others(223): Show |
A | 5 | a0001c0001t0001g0080 a0001c0001t0002g0010 a0001c0001t0002g0024 others(2): Show |
5 | HG02280.hp2 HG03017.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.504-3307_504-3078d others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618671 | |||||||
| chr11:110618751 | G | A | 2 | a0001c0005t0005g0140 a0001c0005t0005g0194 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.504-3157C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618751 | |||||||
| chr11:110618761 | ATATGTAG others(10): Show |
A | 1 | a0001c0008t0003g0099 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.504-3184_504-3168d others(19): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618761 | |||||||
| chr11:110618783 | CAGTGATA others(436): Show |
C | 7 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(4): Show |
8 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.504-3632_504-3190d others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618783 | |||||||
| chr11:110618809 | AGT | A | 2 | a0001c0005t0005g0140 a0001c0005t0005g0194 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.504-3217_504-3216d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618809 | |||||||
| chr11:110618871 | A | C | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0216 |
3 | HG00099.hp1 HG00741.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.504-3277T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618871 | |||||||
| chr11:110618871 | AGTATATG others(453): Show |
A | 74 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(71): Show |
78 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.504-3737_504-3278d others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618871 | |||||||
| chr11:110618874 | ATATGCAG others(161): Show |
A | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3448_504-3281d others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618874 | |||||||
| chr11:110618896 | C | T | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.504-3302G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618896 | |||||||
| chr11:110618901 | G | A | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.504-3307C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618901 | |||||||
| chr11:110618905 | A | C | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.504-3311T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618905 | |||||||
| chr11:110618906 | G | A | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.504-3312C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618906 | |||||||
| chr11:110618906 | GTATATGC others(453): Show |
G | 2 | a0001c0001t0002g0033 a0001c0001t0014g0008 |
2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.504-3772_504-3313d others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618906 | |||||||
| chr11:110618912 | GCAGTGAT others(470): Show |
G | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.504-3795_504-3319d others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618912 | |||||||
| chr11:110618996 | TAGTGATA others(10): Show |
T | 1 | a0001c0008t0003g0099 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.504-3419_504-3403d others(19): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110618996 | |||||||
| chr11:110619008 | G | A | 4 | a0001c0001t0002g0010 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.504-3414C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619008 | |||||||
| chr11:110619038 | G | C | 1 | a0001c0001t0001g0150 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.504-3444C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619038 | |||||||
| chr11:110619059 | A | G | 1 | a0001c0001t0002g0120 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.504-3465T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619059 | |||||||
| chr11:110619064 | C | T | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3470G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619064 | |||||||
| chr11:110619087 | G | A | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3493C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619087 | |||||||
| chr11:110619101 | AGTATATG others(223): Show |
A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0019 others(122): Show |
129 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.504-3737_504-3508d others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619101 | |||||||
| chr11:110619160 | C | T | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3566G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619160 | |||||||
| chr11:110619169 | A | T | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3575T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619169 | |||||||
| chr11:110619172 | ATATGCAG others(138): Show |
A | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3723_504-3579d others(2): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619172 | |||||||
| chr11:110619322 | C | T | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3728G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619322 | |||||||
| chr11:110619331 | G | A | 12 | a0001c0001t0002g0010 a0001c0001t0002g0024 a0001c0001t0002g0025 others(9): Show |
13 | HG02145.hp2 HG02280.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.504-3737C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619331 | |||||||
| chr11:110619360 | G | A | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.504-3766C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619360 | |||||||
| chr11:110619361 | ATAGCATA others(4): Show |
A | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3778_504-3768d others(13): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619361 | |||||||
| chr11:110619376 | A | G | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3782T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619376 | |||||||
| chr11:110619393 | A | G | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3799T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619393 | |||||||
| chr11:110619406 | ATAGAGTA others(10): Show |
A | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.504-3829_504-3813d others(19): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619406 | |||||||
| chr11:110619440 | A | G | 4 | a0001c0001t0002g0064 a0002c0006t0012g0138 a0002c0014t0019g0204 others(1): Show |
4 | HG01952.hp2 HG02257.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.504-3846T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619440 | |||||||
| chr11:110619467 | T | G | 1 | a0009c0021t0005g0217 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.504-3873A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619467 | |||||||
| chr11:110619571 | T | C | 2 | a0002c0006t0012g0138 a0002c0014t0019g0204 |
2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.504-3977A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619571 | |||||||
| chr11:110619580 | C | A | 2 | a0002c0006t0012g0138 a0002c0014t0019g0204 |
2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.504-3986G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619580 | |||||||
| chr11:110619597 | A | C | 2 | a0002c0006t0012g0138 a0002c0014t0019g0204 |
2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.504-4003T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619597 | |||||||
| chr11:110619600 | G | A | 2 | a0002c0006t0012g0138 a0002c0014t0019g0204 |
2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.504-4006C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619600 | |||||||
| chr11:110619634 | A | G | 17 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0006g0154 others(14): Show |
17 | HG00099.hp2 HG00280.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.504-4040T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619634 | |||||||
| chr11:110619645 | T | C | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.504-4051A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619645 | |||||||
| chr11:110619656 | T | C | 2 | a0002c0006t0012g0138 a0002c0014t0019g0204 |
2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.504-4062A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619656 | |||||||
| chr11:110619673 | C | T | 4 | a0001c0001t0003g0209 a0001c0002t0005g0208 a0001c0002t0005g0214 others(1): Show |
4 | HG02015.hp1 HG02080.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.504-4079G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619673 | |||||||
| chr11:110619673 | CAGTGATA others(10): Show |
C | 48 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(45): Show |
52 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.504-4096_504-4080d others(19): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619673 | |||||||
| chr11:110619690 | T | C | 2 | a0002c0006t0012g0138 a0002c0014t0019g0204 |
2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.504-4096A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619690 | |||||||
| chr11:110619705 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.504-4111A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619705 | |||||||
| chr11:110619706 | A | G | 2 | a0002c0006t0012g0138 a0002c0014t0019g0204 |
2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.504-4112T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619706 | |||||||
| chr11:110619707 | C | CAGTGATA others(10): Show |
3 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0044 |
3 | NA18940.hp2 NA18978.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.504-4130_504-4114d others(19): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619707 | |||||||
| chr11:110619707 | C | T | 2 | a0002c0006t0012g0138 a0002c0014t0019g0204 |
2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.504-4113G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619707 | |||||||
| chr11:110619769 | T | C | 2 | a0001c0001t0006g0154 a0012c0017t0002g0139 |
2 | HG02559.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.504-4175A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619769 | |||||||
| chr11:110619958 | T | C | 2 | a0001c0001t0004g0011 a0001c0001t0004g0012 |
2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.503+4204A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110619958 | |||||||
| chr11:110620217 | GA | G | 42 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(39): Show |
46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.503+3944delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620217 | |||||||
| chr11:110620351 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.503+3811T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620351 | |||||||
| chr11:110620353 | A | G | 1 | a0009c0021t0005g0217 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.503+3809T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620353 | |||||||
| chr11:110620374 | CT | C | 2 | a0001c0008t0003g0099 a0001c0008t0003g0100 |
2 | NA19000.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.503+3787delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620374 | |||||||
| chr11:110620376 | C | A | 2 | a0001c0008t0003g0099 a0001c0008t0003g0100 |
2 | NA19000.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.503+3786G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620376 | |||||||
| chr11:110620405 | C | T | 10 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(7): Show |
11 | HG01891.hp1 HG02145.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.503+3757G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620405 | |||||||
| chr11:110620682 | T | C | 1 | a0001c0001t0003g0040 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.503+3480A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620682 | |||||||
| chr11:110620687 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.503+3475T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620687 | |||||||
| chr11:110620800 | G | A | 8 | a0001c0001t0002g0093 a0001c0001t0002g0156 a0001c0001t0002g0157 others(5): Show |
8 | HG00673.hp2 HG02040.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.503+3362C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620800 | |||||||
| chr11:110620995 | A | C | 4 | a0002c0006t0012g0138 a0002c0014t0019g0204 a0003c0004t0002g0142 others(1): Show |
4 | HG01952.hp2 HG03017.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.503+3167T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110620995 | |||||||
| chr11:110621071 | T | C | 4 | a0002c0003t0007g0148 a0007c0018t0015g0009 a0011c0015t0004g0151 others(1): Show |
4 | HG02257.hp1 HG02809.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.503+3091A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621071 | |||||||
| chr11:110621074 | C | CA | 125 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0022 others(122): Show |
130 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.503+3087dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621074 | |||||||
| chr11:110621074 | C | CAA | 17 | a0001c0001t0001g0019 a0001c0001t0001g0058 a0001c0001t0001g0103 others(14): Show |
17 | HG00280.hp1 HG00733.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.503+3086_503+3087d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621074 | |||||||
| chr11:110621232 | G | A | 63 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(60): Show |
67 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.503+2930C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621232 | |||||||
| chr11:110621292 | T | A | 1 | a0001c0002t0005g0113 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.503+2870A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621292 | |||||||
| chr11:110621356 | C | T | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.503+2806G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621356 | |||||||
| chr11:110621359 | G | A | 42 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(39): Show |
46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.503+2803C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621359 | |||||||
| chr11:110621403 | G | C | 1 | a0001c0001t0002g0065 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.503+2759C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621403 | |||||||
| chr11:110621452 | C | CT | 63 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(60): Show |
67 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.503+2709dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621452 | |||||||
| chr11:110621678 | C | T | 4 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.503+2484G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621678 | |||||||
| chr11:110621746 | A | AAGATTGG others(61): Show |
1 | a0001c0001t0008g0016 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.503+2348_503+2415d others(70): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621746 | |||||||
| chr11:110621947 | G | A | 77 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(74): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.503+2215C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621947 | |||||||
| chr11:110621957 | G | A | 77 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(74): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.503+2205C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110621957 | |||||||
| chr11:110622705 | A | G | 1 | a0001c0001t0011g0020 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.503+1457T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110622705 | |||||||
| chr11:110622999 | T | TAAAATTA others(6945): Show |
1 | a0011c0015t0004g0151 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.503+1162_503+1163i others(6954): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110622999 | |||||||
| chr11:110623237 | T | C | 77 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(74): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.503+925A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110623237 | |||||||
| chr11:110623371 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.503+791C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110623371 | |||||||
| chr11:110623377 | T | C | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.503+785A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110623377 | |||||||
| chr11:110623379 | G | A | 2 | a0002c0006t0012g0138 a0002c0014t0019g0204 |
2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.503+783C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110623379 | |||||||
| chr11:110623624 | CTATT | C | 2 | a0001c0005t0005g0140 a0001c0005t0005g0194 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.503+534_503+537del others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110623624 | |||||||
| chr11:110623724 | T | C | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.503+438A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110623724 | |||||||
| chr11:110623788 | GA | G | 48 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(45): Show |
52 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.503+373delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110623788 | |||||||
| chr11:110623852 | CTGTTGTT others(2): Show |
C | 19 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0006g0154 others(16): Show |
19 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.503+301_503+309del others(9): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110623852 | |||||||
| chr11:110624000 | T | C | 35 | a0001c0001t0001g0207 a0001c0001t0002g0200 a0001c0001t0002g0201 others(32): Show |
36 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.503+162A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110624000 | |||||||
| chr11:110624150 | T | C | 6 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(3): Show |
6 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.503+12A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | 110624150 | |||||||
| chr11:110624515 | G | C | 6 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(3): Show |
6 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.354-204C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624515 | |||||||
| chr11:110624552 | T | A | 2 | a0003c0004t0002g0142 a0012c0017t0002g0139 |
2 | HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.354-241A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624552 | |||||||
| chr11:110624560 | A | T | 83 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(80): Show |
88 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.354-249T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624560 | |||||||
| chr11:110624583 | G | A | 2 | a0001c0005t0005g0140 a0001c0005t0005g0194 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.354-272C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624583 | |||||||
| chr11:110624589 | C | T | 2 | a0001c0001t0002g0064 a0008c0016t0002g0062 |
2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.354-278G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624589 | |||||||
| chr11:110624617 | A | G | 35 | a0001c0001t0001g0207 a0001c0001t0002g0200 a0001c0001t0002g0201 others(32): Show |
36 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.354-306T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624617 | |||||||
| chr11:110624626 | G | GT | 42 | a0001c0001t0001g0039 a0001c0001t0002g0028 a0001c0001t0002g0031 others(39): Show |
43 | HG00558.hp2 HG01109.hp2 HG01192.hp2 others(40): Show |
intron_variant | MODIFIER | c.354-316dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624626 | |||||||
| chr11:110624633 | T | C | 6 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0002c0006t0012g0138 others(3): Show |
6 | HG00735.hp2 HG01496.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.354-322A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624633 | |||||||
| chr11:110624829 | T | G | 19 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0006g0154 others(16): Show |
19 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.354-518A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624829 | |||||||
| chr11:110624845 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.354-534G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624845 | |||||||
| chr11:110624877 | G | C | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.354-566C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110624877 | |||||||
| chr11:110625012 | T | TA | 16 | a0001c0001t0002g0096 a0001c0001t0003g0001 a0001c0001t0003g0023 others(13): Show |
18 | HG00323.hp1 HG01099.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.354-702_354-701ins others(1): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625012 | |||||||
| chr11:110625012 | TTTTTTTT others(7): Show |
T | 4 | a0002c0003t0007g0148 a0007c0018t0015g0009 a0011c0015t0004g0151 others(1): Show |
4 | HG02257.hp1 HG02809.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.354-715_354-702del others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625012 | |||||||
| chr11:110625016 | T | A | 16 | a0001c0001t0002g0096 a0001c0001t0003g0001 a0001c0001t0003g0023 others(13): Show |
18 | HG00323.hp1 HG01099.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.354-705A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625016 | |||||||
| chr11:110625016 | T | TA | 26 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0003g0003 others(23): Show |
28 | HG00621.hp2 HG00673.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.354-706_354-705ins others(1): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625016 | |||||||
| chr11:110625017 | TTTATTTT others(8): Show |
T | 31 | a0001c0001t0001g0207 a0001c0001t0002g0200 a0001c0001t0002g0201 others(28): Show |
32 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.354-721_354-707del others(15): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625017 | |||||||
| chr11:110625024 | T | A | 42 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(39): Show |
46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.354-713A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625024 | |||||||
| chr11:110625026 | A | T | 42 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(39): Show |
46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.354-715T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625026 | |||||||
| chr11:110625028 | T | A | 42 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(39): Show |
46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.354-717A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625028 | |||||||
| chr11:110625032 | A | T | 1 | a0001c0001t0001g0039 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.354-721T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625032 | |||||||
| chr11:110625033 | T | A | 35 | a0001c0001t0001g0207 a0001c0001t0002g0200 a0001c0001t0002g0201 others(32): Show |
36 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.354-722A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625033 | |||||||
| chr11:110625033 | T | TTTA | 42 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(39): Show |
46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.354-723_354-722ins others(3): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625033 | |||||||
| chr11:110625034 | T | A | 31 | a0001c0001t0001g0207 a0001c0001t0002g0200 a0001c0001t0002g0201 others(28): Show |
32 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.354-723A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625034 | |||||||
| chr11:110625035 | T | A | 1 | a0001c0001t0021g0177 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.354-724A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625035 | |||||||
| chr11:110625036 | T | A | 5 | a0001c0001t0001g0181 a0001c0001t0002g0037 a0002c0006t0012g0138 others(2): Show |
5 | HG00733.hp2 HG01952.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.354-725A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625036 | |||||||
| chr11:110625037 | T | A | 37 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(34): Show |
41 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.354-726A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625037 | |||||||
| chr11:110625038 | T | A | 7 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0001g0152 others(4): Show |
7 | HG00735.hp2 HG01496.hp2 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.354-727A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625038 | |||||||
| chr11:110625040 | T | C | 10 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.354-729A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625040 | |||||||
| chr11:110625054 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.354-743C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625054 | |||||||
| chr11:110625056 | A | G | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.354-745T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625056 | |||||||
| chr11:110625095 | T | C | 11 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(8): Show |
11 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.354-784A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625095 | |||||||
| chr11:110625123 | C | T | 42 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(39): Show |
46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.354-812G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625123 | |||||||
| chr11:110625192 | C | T | 42 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(39): Show |
46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.354-881G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625192 | |||||||
| chr11:110625239 | T | C | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.354-928A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625239 | |||||||
| chr11:110625283 | C | T | 7 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(4): Show |
8 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.354-972G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625283 | |||||||
| chr11:110625305 | G | T | 42 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(39): Show |
46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.354-994C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625305 | |||||||
| chr11:110625328 | T | C | 85 | a0001c0001t0001g0029 a0001c0001t0001g0130 a0001c0001t0001g0137 others(82): Show |
90 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.354-1017A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625328 | |||||||
| chr11:110625333 | A | G | 77 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(74): Show |
82 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.354-1022T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625333 | |||||||
| chr11:110625378 | G | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.354-1067C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625378 | |||||||
| chr11:110625470 | G | C | 3 | a0001c0001t0003g0023 a0001c0001t0003g0086 a0001c0001t0003g0087 |
3 | NA18954.hp1 NA18999.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.354-1159C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625470 | |||||||
| chr11:110625541 | G | C | 35 | a0001c0001t0001g0207 a0001c0001t0002g0200 a0001c0001t0002g0201 others(32): Show |
36 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.354-1230C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625541 | |||||||
| chr11:110625553 | A | C | 1 | a0001c0001t0008g0016 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.354-1242T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625553 | |||||||
| chr11:110625662 | G | A | 2 | a0001c0001t0003g0067 a0001c0001t0003g0121 |
2 | HG02683.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.354-1351C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625662 | |||||||
| chr11:110625676 | A | T | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.354-1365T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625676 | |||||||
| chr11:110625688 | C | T | 1 | a0001c0002t0005g0212 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.354-1377G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625688 | |||||||
| chr11:110625707 | CAT | C | 42 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(39): Show |
46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.354-1398_354-1397d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625707 | |||||||
| chr11:110625956 | G | A | 35 | a0001c0001t0001g0207 a0001c0001t0002g0200 a0001c0001t0002g0201 others(32): Show |
36 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.354-1645C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110625956 | |||||||
| chr11:110626248 | G | A | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.354-1937C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110626248 | |||||||
| chr11:110626281 | C | T | 4 | a0001c0001t0002g0010 a0001c0001t0002g0024 a0001c0001t0002g0025 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.354-1970G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110626281 | |||||||
| chr11:110626312 | A | C | 1 | a0001c0001t0001g0078 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.354-2001T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110626312 | |||||||
| chr11:110626586 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.354-2275A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110626586 | |||||||
| chr11:110626734 | C | CT | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.354-2424dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110626734 | |||||||
| chr11:110626908 | T | C | 6 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(3): Show |
6 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.354-2597A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110626908 | |||||||
| chr11:110626980 | T | A | 1 | a0001c0001t0002g0031 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.354-2669A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110626980 | |||||||
| chr11:110627099 | T | TA | 35 | a0001c0001t0001g0207 a0001c0001t0002g0200 a0001c0001t0002g0201 others(32): Show |
36 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.354-2789_354-2788i others(3): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627099 | |||||||
| chr11:110627249 | C | T | 41 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(38): Show |
45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.354-2938G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627249 | |||||||
| chr11:110627423 | A | G | 19 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0006g0154 others(16): Show |
19 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.354-3112T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627423 | |||||||
| chr11:110627515 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.353+3113T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627515 | |||||||
| chr11:110627551 | G | A | 6 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(3): Show |
6 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.353+3077C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627551 | |||||||
| chr11:110627599 | C | T | 41 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(38): Show |
45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.353+3029G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627599 | |||||||
| chr11:110627720 | G | A | 3 | a0001c0001t0002g0162 a0001c0001t0002g0163 a0001c0001t0002g0164 |
3 | HG02071.hp2 HG02132.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.353+2908C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627720 | |||||||
| chr11:110627921 | C | A | 1 | a0001c0001t0008g0016 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.353+2707G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627921 | |||||||
| chr11:110627922 | A | C | 1 | a0001c0001t0008g0016 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.353+2706T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627922 | |||||||
| chr11:110627995 | T | C | 35 | a0001c0001t0001g0207 a0001c0001t0002g0200 a0001c0001t0002g0201 others(32): Show |
36 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.353+2633A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110627995 | |||||||
| chr11:110628042 | A | T | 84 | a0001c0001t0001g0029 a0001c0001t0001g0130 a0001c0001t0001g0137 others(81): Show |
89 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.353+2586T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628042 | |||||||
| chr11:110628063 | C | T | 12 | a0001c0001t0002g0075 a0001c0001t0004g0006 a0001c0001t0004g0011 others(9): Show |
13 | HG01891.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.353+2565G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628063 | |||||||
| chr11:110628130 | T | A | 84 | a0001c0001t0001g0029 a0001c0001t0001g0130 a0001c0001t0001g0137 others(81): Show |
89 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.353+2498A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628130 | |||||||
| chr11:110628283 | C | T | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.353+2345G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628283 | |||||||
| chr11:110628457 | T | C | 7 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(4): Show |
8 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.353+2171A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628457 | |||||||
| chr11:110628482 | A | T | 1 | a0002c0014t0019g0204 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.353+2146T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628482 | |||||||
| chr11:110628527 | A | C | 1 | a0001c0001t0002g0041 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.353+2101T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628527 | |||||||
| chr11:110628530 | A | C | 73 | a0001c0001t0001g0039 a0001c0001t0001g0153 a0001c0001t0002g0010 others(70): Show |
74 | HG00558.hp2 HG00673.hp2 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.353+2098T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628530 | |||||||
| chr11:110628533 | C | A | 2 | a0002c0006t0012g0138 a0002c0014t0019g0204 |
2 | HG01952.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.353+2095G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628533 | |||||||
| chr11:110628609 | G | A | 5 | a0001c0001t0002g0042 a0001c0001t0002g0043 a0001c0001t0002g0044 others(2): Show |
5 | NA18940.hp2 NA18978.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.353+2019C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628609 | |||||||
| chr11:110628742 | AAAGTT | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.353+1881_353+1885d others(7): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628742 | |||||||
| chr11:110628813 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | NA19065.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.353+1815T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628813 | |||||||
| chr11:110628871 | C | A | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.353+1757G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628871 | |||||||
| chr11:110628965 | C | A | 76 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(73): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.353+1663G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110628965 | |||||||
| chr11:110629030 | G | C | 1 | a0001c0001t0002g0041 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.353+1598C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629030 | |||||||
| chr11:110629038 | A | C | 6 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(3): Show |
6 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.353+1590T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629038 | |||||||
| chr11:110629158 | CTATT | C | 41 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(38): Show |
45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.353+1466_353+1469d others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629158 | |||||||
| chr11:110629227 | C | T | 1 | a0001c0001t0003g0015 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.353+1401G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629227 | |||||||
| chr11:110629498 | C | A | 1 | a0001c0001t0008g0016 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.353+1130G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629498 | |||||||
| chr11:110629528 | A | T | 84 | a0001c0001t0001g0029 a0001c0001t0001g0130 a0001c0001t0001g0137 others(81): Show |
89 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.353+1100T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629528 | |||||||
| chr11:110629551 | T | TA | 62 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(59): Show |
66 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.353+1076dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629551 | |||||||
| chr11:110629561 | T | A | 84 | a0001c0001t0001g0029 a0001c0001t0001g0130 a0001c0001t0001g0137 others(81): Show |
89 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.353+1067A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629561 | |||||||
| chr11:110629597 | G | T | 15 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0006g0154 others(12): Show |
15 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.353+1031C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629597 | |||||||
| chr11:110629602 | G | A | 76 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(73): Show |
81 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.353+1026C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629602 | |||||||
| chr11:110629881 | G | T | 2 | a0001c0005t0005g0140 a0001c0005t0005g0194 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.353+747C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629881 | |||||||
| chr11:110629987 | A | G | 1 | a0002c0003t0007g0148 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.353+641T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110629987 | |||||||
| chr11:110630036 | T | C | 1 | a0001c0001t0002g0034 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.353+592A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110630036 | |||||||
| chr11:110630245 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.353+383A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110630245 | |||||||
| chr11:110630275 | A | G | 62 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(59): Show |
66 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.353+353T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110630275 | |||||||
| chr11:110630312 | C | T | 1 | a0001c0001t0003g0040 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.353+316G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110630312 | |||||||
| chr11:110630421 | CATGGCAC others(7): Show |
C | 14 | a0001c0001t0004g0006 a0001c0001t0004g0011 a0001c0001t0004g0012 others(11): Show |
15 | HG01891.hp1 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.353+193_353+206del others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110630421 | |||||||
| chr11:110630473 | AT | A | 41 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(38): Show |
45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.353+154delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 3/14 | chr11 | 110630473 | |||||||
| chr11:110630975 | T | C | 16 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(13): Show |
16 | HG01074.hp1 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.189-183A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110630975 | |||||||
| chr11:110631049 | C | T | 84 | a0001c0001t0001g0029 a0001c0001t0001g0130 a0001c0001t0001g0137 others(81): Show |
89 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.189-257G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110631049 | |||||||
| chr11:110631106 | T | C | 10 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(7): Show |
10 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.189-314A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110631106 | |||||||
| chr11:110631160 | T | G | 60 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(57): Show |
64 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.189-368A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110631160 | |||||||
| chr11:110631203 | C | A | 26 | a0001c0001t0001g0207 a0001c0001t0002g0200 a0001c0001t0002g0201 others(23): Show |
27 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.189-411G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110631203 | |||||||
| chr11:110631383 | T | C | 42 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(39): Show |
46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.189-591A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110631383 | |||||||
| chr11:110631550 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.189-758G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110631550 | |||||||
| chr11:110631693 | T | C | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-901A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110631693 | |||||||
| chr11:110631736 | C | T | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-944G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110631736 | |||||||
| chr11:110631943 | C | A | 1 | a0008c0016t0002g0062 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.189-1151G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110631943 | |||||||
| chr11:110632230 | A | T | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-1438T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632230 | |||||||
| chr11:110632233 | A | T | 121 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0130 others(118): Show |
125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.189-1441T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632233 | |||||||
| chr11:110632352 | C | G | 1 | a0001c0001t0001g0161 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.189-1560G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632352 | |||||||
| chr11:110632587 | T | A | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.189-1795A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632587 | |||||||
| chr11:110632625 | G | A | 2 | a0001c0001t0002g0201 a0001c0001t0002g0202 |
2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.189-1833C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632625 | |||||||
| chr11:110632743 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.189-1951A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632743 | |||||||
| chr11:110632803 | G | C | 5 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-2011C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632803 | |||||||
| chr11:110632817 | G | A | 127 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0130 others(124): Show |
132 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.189-2025C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632817 | |||||||
| chr11:110632898 | AT | A | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0002c0006t0012g0138 others(1): Show |
5 | HG01952.hp2 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-2107delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632898 | |||||||
| chr11:110632902 | GTTTTGGA others(5): Show |
G | 2 | a0001c0005t0005g0140 a0001c0005t0005g0194 |
2 | HG01891.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.189-2122_189-2111d others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110632902 | |||||||
| chr11:110633048 | C | T | 1 | a0003c0004t0002g0142 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.189-2256G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110633048 | |||||||
| chr11:110633321 | T | C | 60 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(57): Show |
64 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.189-2529A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110633321 | |||||||
| chr11:110633347 | C | T | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-2555G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110633347 | |||||||
| chr11:110633582 | A | G | 6 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(3): Show |
6 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.189-2790T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110633582 | |||||||
| chr11:110633710 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.189-2918C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110633710 | |||||||
| chr11:110634034 | C | A | 1 | a0001c0001t0001g0123 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.189-3242G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110634034 | |||||||
| chr11:110634088 | A | G | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-3296T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110634088 | |||||||
| chr11:110634148 | A | G | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-3356T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110634148 | |||||||
| chr11:110634289 | G | A | 41 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(38): Show |
45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.189-3497C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110634289 | |||||||
| chr11:110634656 | A | C | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-3864T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110634656 | |||||||
| chr11:110634742 | C | T | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-3950G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110634742 | |||||||
| chr11:110634942 | GT | G | 121 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0130 others(118): Show |
125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.189-4151delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110634942 | |||||||
| chr11:110634970 | T | C | 3 | a0001c0001t0006g0196 a0001c0001t0006g0197 a0001c0001t0006g0198 |
3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.189-4178A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110634970 | |||||||
| chr11:110634998 | G | A | 121 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0130 others(118): Show |
125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.189-4206C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110634998 | |||||||
| chr11:110635096 | C | A | 1 | a0001c0001t0002g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.189-4304G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110635096 | |||||||
| chr11:110635438 | T | A | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-4646A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110635438 | |||||||
| chr11:110635438 | T | G | 120 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0130 others(117): Show |
124 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.189-4646A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110635438 | |||||||
| chr11:110635683 | T | A | 121 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0130 others(118): Show |
125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.189-4891A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110635683 | |||||||
| chr11:110635785 | T | A | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0002c0006t0012g0138 others(1): Show |
5 | HG01952.hp2 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-4993A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110635785 | |||||||
| chr11:110635790 | G | GA | 6 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(3): Show |
6 | HG01074.hp1 HG01891.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.189-4999dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110635790 | |||||||
| chr11:110636201 | G | A | 1 | a0002c0003t0007g0205 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.189-5409C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110636201 | |||||||
| chr11:110636217 | G | A | 121 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0130 others(118): Show |
125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.189-5425C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110636217 | |||||||
| chr11:110636276 | G | A | 121 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0130 others(118): Show |
125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.189-5484C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110636276 | |||||||
| chr11:110636306 | T | A | 1 | a0001c0001t0002g0041 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.189-5514A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110636306 | |||||||
| chr11:110636542 | C | G | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-5750G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110636542 | |||||||
| chr11:110636750 | C | A | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-5958G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110636750 | |||||||
| chr11:110636967 | C | A | 8 | a0001c0001t0003g0001 a0001c0001t0003g0023 a0001c0001t0003g0051 others(5): Show |
10 | HG01928.hp2 HG01981.hp2 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-6175G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110636967 | |||||||
| chr11:110637009 | C | T | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0002c0006t0012g0138 others(1): Show |
5 | HG01952.hp2 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-6217G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637009 | |||||||
| chr11:110637153 | C | T | 72 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0207 others(69): Show |
72 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.189-6361G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637153 | |||||||
| chr11:110637317 | G | A | 49 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(46): Show |
53 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.189-6525C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637317 | |||||||
| chr11:110637423 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.189-6631G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637423 | |||||||
| chr11:110637435 | ATTAG | A | 2 | a0001c0001t0002g0074 a0001c0001t0016g0059 |
2 | HG03239.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.189-6647_189-6644d others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637435 | |||||||
| chr11:110637444 | A | T | 120 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0130 others(117): Show |
124 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.189-6652T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637444 | |||||||
| chr11:110637526 | G | A | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0002c0006t0012g0138 others(1): Show |
5 | HG01952.hp2 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-6734C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637526 | |||||||
| chr11:110637611 | G | A | 2 | a0001c0001t0013g0110 a0001c0001t0013g0187 |
2 | HG02015.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.189-6819C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637611 | |||||||
| chr11:110637617 | A | T | 121 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0130 others(118): Show |
125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.189-6825T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637617 | |||||||
| chr11:110637738 | A | G | 121 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0130 others(118): Show |
125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.189-6946T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110637738 | |||||||
| chr11:110638130 | T | G | 1 | a0001c0001t0001g0027 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.189-7338A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638130 | |||||||
| chr11:110638341 | A | T | 8 | a0001c0001t0002g0093 a0001c0001t0002g0156 a0001c0001t0002g0157 others(5): Show |
8 | HG00673.hp2 HG02040.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.189-7549T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638341 | |||||||
| chr11:110638444 | C | T | 118 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0130 others(115): Show |
122 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.189-7652G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638444 | |||||||
| chr11:110638512 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.189-7720C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638512 | |||||||
| chr11:110638604 | C | G | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-7812G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638604 | |||||||
| chr11:110638618 | G | A | 1 | a0001c0001t0004g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.189-7826C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638618 | |||||||
| chr11:110638751 | C | CA | 10 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-7960dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638751 | |||||||
| chr11:110638814 | T | C | 115 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0130 others(112): Show |
119 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.189-8022A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638814 | |||||||
| chr11:110638887 | T | C | 7 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0001t0004g0006 others(4): Show |
8 | HG01891.hp2 HG01952.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.189-8095A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110638887 | |||||||
| chr11:110639033 | C | T | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-8241G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639033 | |||||||
| chr11:110639141 | C | T | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-8349G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639141 | |||||||
| chr11:110639201 | G | A | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-8409C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639201 | |||||||
| chr11:110639238 | AC | A | 13 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(10): Show |
14 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.189-8447delG | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639238 | |||||||
| chr11:110639238 | ACC | A | 64 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0001g0207 others(61): Show |
64 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.189-8448_189-8447d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639238 | |||||||
| chr11:110639247 | C | CG | 9 | a0001c0001t0003g0066 a0001c0001t0006g0154 a0001c0001t0006g0196 others(6): Show |
9 | HG01261.hp2 HG02109.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.189-8456_189-8455i others(3): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639247 | |||||||
| chr11:110639247 | C | G | 41 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(38): Show |
45 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.189-8455G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639247 | |||||||
| chr11:110639249 | A | AC | 3 | a0001c0001t0001g0007 a0001c0001t0001g0172 a0001c0001t0001g0190 |
4 | HG02622.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-8458dupG | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639249 | |||||||
| chr11:110639307 | T | C | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-8515A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639307 | |||||||
| chr11:110639381 | CT | C | 12 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0003g0067 others(9): Show |
12 | HG00735.hp2 HG01496.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.189-8590delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639381 | |||||||
| chr11:110639444 | T | C | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.189-8652A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639444 | |||||||
| chr11:110639484 | C | T | 131 | a0001c0001t0001g0029 a0001c0001t0001g0039 a0001c0001t0001g0049 others(128): Show |
136 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.189-8692G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639484 | |||||||
| chr11:110639578 | A | G | 7 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0001t0004g0006 others(4): Show |
8 | HG01891.hp2 HG01952.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.189-8786T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639578 | |||||||
| chr11:110639579 | T | C | 3 | a0001c0001t0002g0200 a0002c0003t0007g0199 a0002c0003t0007g0205 |
3 | HG01074.hp1 HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.189-8787A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639579 | |||||||
| chr11:110639637 | T | A | 1 | a0001c0001t0003g0066 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.189-8845A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639637 | |||||||
| chr11:110639753 | G | T | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-8961C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639753 | |||||||
| chr11:110639791 | A | G | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-8999T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639791 | |||||||
| chr11:110639804 | C | T | 3 | a0001c0001t0002g0200 a0002c0003t0007g0199 a0002c0003t0007g0205 |
3 | HG01074.hp1 HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.189-9012G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639804 | |||||||
| chr11:110639992 | T | G | 53 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(50): Show |
57 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.189-9200A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110639992 | |||||||
| chr11:110640129 | T | A | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0002c0006t0012g0138 others(1): Show |
5 | HG01952.hp2 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-9337A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110640129 | |||||||
| chr11:110640191 | C | G | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-9399G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110640191 | |||||||
| chr11:110640325 | C | G | 20 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0002g0026 others(17): Show |
20 | HG00558.hp2 HG01358.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.189-9533G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110640325 | |||||||
| chr11:110640423 | G | C | 3 | a0001c0001t0002g0200 a0002c0003t0007g0199 a0002c0003t0007g0205 |
3 | HG01074.hp1 HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.189-9631C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110640423 | |||||||
| chr11:110640527 | C | T | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.189-9735G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110640527 | |||||||
| chr11:110640867 | C | T | 66 | a0001c0001t0001g0130 a0001c0001t0001g0207 a0001c0001t0002g0010 others(63): Show |
68 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.189-10075G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110640867 | |||||||
| chr11:110640876 | C | T | 79 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0001g0207 others(76): Show |
83 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.189-10084G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110640876 | |||||||
| chr11:110640899 | T | C | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-10107A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110640899 | |||||||
| chr11:110641088 | A | G | 42 | a0001c0001t0001g0130 a0001c0001t0001g0161 a0001c0001t0002g0096 others(39): Show |
46 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.189-10296T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110641088 | |||||||
| chr11:110641099 | C | T | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-10307G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110641099 | |||||||
| chr11:110641606 | G | C | 1 | a0001c0001t0003g0047 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.189-10814C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110641606 | |||||||
| chr11:110641755 | T | C | 7 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(4): Show |
7 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-10963A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110641755 | |||||||
| chr11:110641906 | T | C | 90 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.189-11114A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110641906 | |||||||
| chr11:110641913 | G | A | 90 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.189-11121C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110641913 | |||||||
| chr11:110641923 | T | C | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-11131A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110641923 | |||||||
| chr11:110642068 | G | A | 1 | a0001c0001t0003g0085 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.189-11276C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642068 | |||||||
| chr11:110642072 | T | G | 97 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(94): Show |
99 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.189-11280A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642072 | |||||||
| chr11:110642167 | T | G | 13 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0002g0201 others(10): Show |
14 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.189-11375A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642167 | |||||||
| chr11:110642218 | G | A | 4 | a0001c0001t0002g0200 a0002c0003t0007g0199 a0002c0003t0007g0205 others(1): Show |
4 | HG01074.hp1 HG01952.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-11426C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642218 | |||||||
| chr11:110642230 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.189-11438G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642230 | |||||||
| chr11:110642326 | G | A | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-11534C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642326 | |||||||
| chr11:110642353 | C | T | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-11561G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642353 | |||||||
| chr11:110642469 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-11677G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642469 | |||||||
| chr11:110642698 | C | T | 95 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(92): Show |
97 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.189-11906G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642698 | |||||||
| chr11:110642701 | G | A | 1 | a0001c0001t0018g0084 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.189-11909C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642701 | |||||||
| chr11:110642827 | C | T | 1 | a0001c0001t0004g0095 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.189-12035G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642827 | |||||||
| chr11:110642979 | G | A | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.189-12187C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642979 | |||||||
| chr11:110642984 | A | G | 5 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0021g0177 others(2): Show |
5 | HG01981.hp1 NA18962.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-12192T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110642984 | |||||||
| chr11:110643012 | C | T | 6 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(3): Show |
6 | HG00735.hp2 HG01496.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-12220G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643012 | |||||||
| chr11:110643201 | G | C | 10 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0004g0006 others(7): Show |
11 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.189-12409C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643201 | |||||||
| chr11:110643233 | T | C | 92 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(89): Show |
94 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.189-12441A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643233 | |||||||
| chr11:110643373 | G | C | 1 | a0001c0001t0009g0004 | 2 | HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.189-12581C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643373 | |||||||
| chr11:110643394 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.189-12602C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643394 | |||||||
| chr11:110643408 | C | T | 91 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(88): Show |
93 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.189-12616G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643408 | |||||||
| chr11:110643453 | G | C | 1 | a0001c0001t0016g0059 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.189-12661C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643453 | |||||||
| chr11:110643489 | C | T | 1 | a0002c0003t0007g0203 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.189-12697G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643489 | |||||||
| chr11:110643594 | A | T | 10 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-12802T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643594 | |||||||
| chr11:110643611 | T | C | 10 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-12819A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643611 | |||||||
| chr11:110643643 | AT | A | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-12852delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110643643 | |||||||
| chr11:110644115 | A | T | 95 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(92): Show |
97 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.189-13323T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644115 | |||||||
| chr11:110644337 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.189-13545C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644337 | |||||||
| chr11:110644341 | T | G | 13 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0002g0201 others(10): Show |
14 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.189-13549A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644341 | |||||||
| chr11:110644362 | A | G | 2 | a0001c0001t0002g0201 a0001c0001t0002g0202 |
2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.189-13570T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644362 | |||||||
| chr11:110644532 | G | A | 4 | a0001c0001t0002g0200 a0002c0003t0007g0199 a0002c0003t0007g0205 others(1): Show |
4 | HG01074.hp1 HG01952.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-13740C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644532 | |||||||
| chr11:110644544 | A | G | 84 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(81): Show |
85 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.189-13752T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644544 | |||||||
| chr11:110644785 | T | A | 95 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(92): Show |
97 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.189-13993A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644785 | |||||||
| chr11:110644997 | T | TTCTATCT others(9): Show |
2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-14206_189-1420 others(20): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644997 | |||||||
| chr11:110644997 | T | TTCTC | 77 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(74): Show |
78 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.189-14209_189-1420 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644997 | |||||||
| chr11:110644997 | T | TTCTCTCT others(3): Show |
3 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0002c0003t0007g0203 |
3 | HG01891.hp2 HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.189-14215_189-1420 others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644997 | |||||||
| chr11:110644997 | T | TTCTCTCT others(5): Show |
4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-14217_189-1420 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110644997 | |||||||
| chr11:110645171 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.189-14379G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110645171 | |||||||
| chr11:110645302 | G | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-14510C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110645302 | |||||||
| chr11:110645505 | C | A | 5 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-14713G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110645505 | |||||||
| chr11:110645547 | T | C | 1 | a0001c0001t0002g0065 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.189-14755A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110645547 | |||||||
| chr11:110645652 | G | C | 1 | a0001c0002t0005g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.189-14860C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110645652 | |||||||
| chr11:110645763 | T | C | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-14971A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110645763 | |||||||
| chr11:110645847 | T | C | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.189-15055A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110645847 | |||||||
| chr11:110645887 | A | G | 80 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.189-15095T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110645887 | |||||||
| chr11:110645959 | A | G | 76 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(73): Show |
77 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.189-15167T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110645959 | |||||||
| chr11:110646002 | A | G | 1 | a0001c0001t0003g0069 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.189-15210T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110646002 | |||||||
| chr11:110646012 | G | C | 52 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(49): Show |
53 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.189-15220C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110646012 | |||||||
| chr11:110646100 | T | A | 76 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(73): Show |
77 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.189-15308A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110646100 | |||||||
| chr11:110646401 | G | C | 1 | a0001c0001t0001g0117 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.189-15609C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110646401 | |||||||
| chr11:110646439 | C | T | 1 | a0001c0001t0003g0092 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.189-15647G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110646439 | |||||||
| chr11:110646529 | T | C | 10 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-15737A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110646529 | |||||||
| chr11:110646570 | A | C | 92 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(89): Show |
94 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.189-15778T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110646570 | |||||||
| chr11:110646952 | A | C | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-16160T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110646952 | |||||||
| chr11:110647159 | T | TTG | 6 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(3): Show |
6 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-16369_189-1636 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110647159 | |||||||
| chr11:110647516 | G | C | 1 | a0002c0003t0007g0205 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.189-16724C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110647516 | |||||||
| chr11:110647705 | A | C | 88 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(85): Show |
90 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.189-16913T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110647705 | |||||||
| chr11:110647816 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-17024G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110647816 | |||||||
| chr11:110647954 | A | C | 1 | a0001c0001t0001g0077 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.189-17162T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110647954 | |||||||
| chr11:110648153 | T | TAATATAT others(31): Show |
1 | a0001c0001t0003g0081 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.189-17399_189-1736 others(42): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648153 | |||||||
| chr11:110648154 | AAT | A | 2 | a0001c0005t0005g0194 a0007c0018t0015g0009 |
2 | HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.189-17364_189-1736 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648154 | |||||||
| chr11:110648154 | AATATATA others(13): Show |
A | 1 | a0001c0001t0011g0020 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.189-17382_189-1736 others(24): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648154 | |||||||
| chr11:110648166 | TATGTAA | T | 6 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(3): Show |
6 | HG00280.hp2 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.189-17380_189-1737 others(10): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648166 | |||||||
| chr11:110648167 | A | G | 62 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(59): Show |
63 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.189-17375T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648167 | |||||||
| chr11:110648168 | TGTAA | T | 62 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(59): Show |
63 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.189-17380_189-1737 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648168 | |||||||
| chr11:110648170 | TA | T | 4 | a0001c0001t0002g0125 a0001c0001t0003g0015 a0001c0001t0003g0133 others(1): Show |
4 | HG01433.hp2 HG01516.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-17379delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648170 | |||||||
| chr11:110648172 | A | AAT | 8 | a0001c0001t0001g0002 a0001c0001t0001g0029 a0001c0001t0001g0073 others(5): Show |
8 | HG00735.hp2 HG01496.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.189-17382_189-1738 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648172 | |||||||
| chr11:110648172 | A | AATATATA others(33): Show |
1 | a0001c0001t0001g0088 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.189-17420_189-1738 others(44): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648172 | |||||||
| chr11:110648172 | A | C | 4 | a0001c0005t0005g0194 a0005c0007t0010g0145 a0005c0007t0010g0146 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-17380T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648172 | |||||||
| chr11:110648172 | AAT | A | 39 | a0001c0001t0001g0097 a0001c0001t0001g0130 a0001c0001t0002g0024 others(36): Show |
43 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.189-17382_189-1738 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648172 | |||||||
| chr11:110648173 | A | G | 6 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(3): Show |
6 | HG00280.hp2 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.189-17381T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648173 | |||||||
| chr11:110648174 | T | C | 62 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(59): Show |
63 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.189-17382A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648174 | |||||||
| chr11:110648174 | TATATATA others(73): Show |
T | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.189-17462_189-1738 others(84): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648174 | |||||||
| chr11:110648176 | T | C | 6 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(3): Show |
6 | HG00280.hp2 HG02145.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.189-17384A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648176 | |||||||
| chr11:110648176 | TATATATA others(9): Show |
T | 1 | a0002c0003t0007g0199 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.189-17400_189-1738 others(20): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648176 | |||||||
| chr11:110648176 | TATATATA others(71): Show |
T | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-17462_189-1738 others(82): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648176 | |||||||
| chr11:110648187 | A | G | 4 | a0001c0001t0003g0066 a0001c0001t0003g0090 a0005c0007t0010g0145 others(1): Show |
4 | HG01261.hp2 HG02602.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-17395T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648187 | |||||||
| chr11:110648188 | TGTAA | T | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-17400_189-1739 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648188 | |||||||
| chr11:110648189 | G | A | 2 | a0001c0001t0003g0066 a0001c0001t0003g0090 |
2 | HG01261.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.189-17397C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648189 | |||||||
| chr11:110648190 | T | A | 2 | a0001c0001t0003g0066 a0001c0001t0003g0090 |
2 | HG01261.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.189-17398A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648190 | |||||||
| chr11:110648192 | A | C | 77 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(74): Show |
79 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.189-17400T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648192 | |||||||
| chr11:110648192 | A | T | 2 | a0001c0001t0003g0066 a0001c0001t0003g0090 |
2 | HG01261.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.189-17400T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648192 | |||||||
| chr11:110648192 | AAT | A | 5 | a0001c0001t0001g0097 a0001c0001t0002g0055 a0001c0001t0003g0005 others(2): Show |
5 | HG01192.hp1 HG02145.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.189-17402_189-1740 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648192 | |||||||
| chr11:110648194 | T | C | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-17402A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648194 | |||||||
| chr11:110648194 | TATATATA others(53): Show |
T | 69 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(66): Show |
70 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.189-17462_189-1740 others(64): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648194 | |||||||
| chr11:110648198 | TATATATA others(5): Show |
T | 1 | a0001c0001t0002g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.189-17418_189-1740 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648198 | |||||||
| chr11:110648205 | A | G | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-17413T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648205 | |||||||
| chr11:110648207 | G | A | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-17415C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648207 | |||||||
| chr11:110648208 | T | C | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-17416A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648208 | |||||||
| chr11:110648210 | A | T | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-17418T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648210 | |||||||
| chr11:110648210 | AATATATA others(5): Show |
A | 1 | a0001c0001t0003g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.189-17430_189-1741 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648210 | |||||||
| chr11:110648210 | AATATATA others(9): Show |
A | 1 | a0001c0001t0003g0109 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.189-17434_189-1741 others(20): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648210 | |||||||
| chr11:110648210 | AATATATA others(11): Show |
A | 6 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(3): Show |
6 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-17436_189-1741 others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648210 | |||||||
| chr11:110648215 | ATATATG | A | 6 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
7 | HG00280.hp1 HG00639.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.189-17429_189-1742 others(10): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648215 | |||||||
| chr11:110648221 | G | A | 10 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0002c0003t0007g0148 others(7): Show |
10 | HG00735.hp2 HG01496.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-17429C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648221 | |||||||
| chr11:110648221 | GTA | G | 57 | a0001c0001t0001g0078 a0001c0001t0001g0097 a0001c0001t0001g0130 others(54): Show |
60 | HG00621.hp2 HG00673.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.189-17431_189-1743 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648221 | |||||||
| chr11:110648221 | GTATA | G | 4 | a0001c0001t0001g0091 a0001c0001t0003g0005 a0001c0001t0003g0069 others(1): Show |
4 | HG02602.hp2 HG02738.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-17433_189-1743 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648221 | |||||||
| chr11:110648223 | A | G | 10 | a0001c0001t0001g0029 a0001c0001t0001g0105 a0001c0001t0001g0137 others(7): Show |
10 | HG00735.hp2 HG01496.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-17431T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648223 | |||||||
| chr11:110648224 | T | A | 2 | a0001c0001t0002g0010 a0001c0001t0006g0154 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.189-17432A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648224 | |||||||
| chr11:110648224 | T | C | 7 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0001t0006g0196 others(4): Show |
8 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.189-17432A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648224 | |||||||
| chr11:110648225 | A | G | 1 | a0002c0003t0007g0199 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.189-17433T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648225 | |||||||
| chr11:110648226 | T | C | 9 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0002c0003t0007g0148 others(6): Show |
9 | HG00735.hp2 HG01496.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.189-17434A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648226 | |||||||
| chr11:110648226 | T | TATATATA others(19): Show |
1 | a0001c0001t0002g0025 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.189-17435_189-1743 others(30): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648226 | |||||||
| chr11:110648226 | TATATATA others(7): Show |
T | 7 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0001t0006g0196 others(4): Show |
8 | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.189-17448_189-1743 others(18): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648226 | |||||||
| chr11:110648228 | T | A | 1 | a0002c0003t0007g0199 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.189-17436A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648228 | |||||||
| chr11:110648228 | TATATATA others(5): Show |
T | 3 | a0002c0003t0007g0148 a0011c0015t0004g0151 a0013c0019t0004g0149 |
3 | HG02257.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.189-17448_189-1743 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648228 | |||||||
| chr11:110648237 | G | T | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-17445C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648237 | |||||||
| chr11:110648240 | A | C | 15 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0002g0010 others(12): Show |
15 | HG00735.hp2 HG01074.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.189-17448T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648240 | |||||||
| chr11:110648242 | TATATATA others(5): Show |
T | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-17462_189-1745 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648242 | |||||||
| chr11:110648244 | TATATATG others(3): Show |
T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-17462_189-1745 others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648244 | |||||||
| chr11:110648254 | A | C | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-17462T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648254 | |||||||
| chr11:110648265 | G | T | 70 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(67): Show |
71 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.189-17473C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648265 | |||||||
| chr11:110648268 | A | C | 78 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(75): Show |
80 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.189-17476T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648268 | |||||||
| chr11:110648348 | G | A | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-17556C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648348 | |||||||
| chr11:110648351 | T | C | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-17559A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648351 | |||||||
| chr11:110648353 | C | CAT | 185 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(182): Show |
191 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.189-17563_189-1756 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648353 | |||||||
| chr11:110648353 | C | T | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-17561G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648353 | |||||||
| chr11:110648484 | A | AT | 46 | a0001c0001t0001g0049 a0001c0001t0001g0097 a0001c0001t0001g0127 others(43): Show |
50 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.189-17693dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648484 | |||||||
| chr11:110648484 | AT | A | 64 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(61): Show |
66 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.189-17693delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648484 | |||||||
| chr11:110648615 | A | G | 84 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(81): Show |
86 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.189-17823T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648615 | |||||||
| chr11:110648671 | C | T | 70 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(67): Show |
71 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.189-17879G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648671 | |||||||
| chr11:110648979 | T | C | 5 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-18187A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110648979 | |||||||
| chr11:110649201 | C | CT | 14 | a0001c0001t0001g0039 a0001c0001t0001g0131 a0001c0001t0002g0028 others(11): Show |
14 | HG00673.hp1 HG01109.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.189-18410dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649201 | |||||||
| chr11:110649201 | CT | C | 23 | a0001c0001t0001g0130 a0001c0001t0001g0152 a0001c0001t0002g0032 others(20): Show |
23 | HG00280.hp2 HG01074.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.189-18410delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649201 | |||||||
| chr11:110649201 | CTT | C | 15 | a0001c0001t0001g0029 a0001c0001t0001g0135 a0001c0001t0001g0137 others(12): Show |
16 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.189-18411_189-1841 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649201 | |||||||
| chr11:110649201 | CTTT | C | 42 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(39): Show |
43 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.189-18412_189-1841 others(7): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649201 | |||||||
| chr11:110649201 | CTTTTTTT others(5): Show |
C | 9 | a0001c0001t0001g0155 a0001c0001t0001g0165 a0001c0001t0001g0173 others(6): Show |
9 | HG01981.hp1 HG02165.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.189-18421_189-1841 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649201 | |||||||
| chr11:110649369 | A | C | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.189-18577T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649369 | |||||||
| chr11:110649394 | G | A | 70 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(67): Show |
71 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.189-18602C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649394 | |||||||
| chr11:110649417 | A | T | 1 | a0001c0001t0001g0165 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.189-18625T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649417 | |||||||
| chr11:110649567 | G | A | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-18775C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649567 | |||||||
| chr11:110649635 | G | A | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-18843C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649635 | |||||||
| chr11:110649656 | G | C | 5 | a0001c0001t0002g0031 a0001c0001t0002g0035 a0001c0001t0002g0036 others(2): Show |
5 | HG01109.hp2 HG02486.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-18864C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649656 | |||||||
| chr11:110649828 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.189-19036T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110649828 | |||||||
| chr11:110650146 | T | C | 9 | a0001c0001t0002g0028 a0001c0001t0002g0031 a0001c0001t0002g0033 others(6): Show |
9 | HG01109.hp2 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.189-19354A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650146 | |||||||
| chr11:110650215 | T | C | 97 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(94): Show |
99 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.189-19423A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650215 | |||||||
| chr11:110650218 | T | C | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-19426A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650218 | |||||||
| chr11:110650237 | C | A | 1 | a0006c0011t0002g0126 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.189-19445G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650237 | |||||||
| chr11:110650424 | G | C | 7 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(4): Show |
7 | HG02145.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.189-19632C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650424 | |||||||
| chr11:110650703 | T | C | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-19911A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650703 | |||||||
| chr11:110650741 | A | G | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-19949T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650741 | |||||||
| chr11:110650837 | A | G | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-20045T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650837 | |||||||
| chr11:110650852 | G | A | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-20060C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650852 | |||||||
| chr11:110650884 | T | C | 67 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(64): Show |
68 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.189-20092A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650884 | |||||||
| chr11:110650904 | C | T | 1 | a0002c0003t0007g0205 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.189-20112G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650904 | |||||||
| chr11:110650909 | A | G | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-20117T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110650909 | |||||||
| chr11:110651035 | G | C | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-20243C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651035 | |||||||
| chr11:110651193 | A | C | 1 | a0001c0001t0006g0154 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.189-20401T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651193 | |||||||
| chr11:110651324 | C | A | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-20532G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651324 | |||||||
| chr11:110651400 | C | A | 69 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(66): Show |
70 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.189-20608G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651400 | |||||||
| chr11:110651453 | T | G | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-20661A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651453 | |||||||
| chr11:110651747 | C | CA | 19 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0002g0028 others(16): Show |
19 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.189-20956dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651747 | |||||||
| chr11:110651747 | CA | C | 72 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(69): Show |
73 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.189-20956delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651747 | |||||||
| chr11:110651747 | CAA | C | 6 | a0001c0001t0001g0191 a0001c0001t0004g0013 a0001c0001t0004g0014 others(3): Show |
6 | HG02145.hp2 HG02809.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-20957_189-2095 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651747 | |||||||
| chr11:110651856 | G | C | 1 | a0001c0001t0001g0022 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.189-21064C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651856 | |||||||
| chr11:110651873 | C | T | 7 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(4): Show |
7 | HG02145.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.189-21081G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651873 | |||||||
| chr11:110651886 | T | C | 79 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.189-21094A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110651886 | |||||||
| chr11:110652093 | T | C | 6 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(3): Show |
7 | HG01891.hp1 HG02622.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-21301A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652093 | |||||||
| chr11:110652101 | T | C | 78 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(75): Show |
79 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.189-21309A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652101 | |||||||
| chr11:110652304 | G | A | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-21512C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652304 | |||||||
| chr11:110652321 | C | G | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.189-21529G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652321 | |||||||
| chr11:110652490 | C | T | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.189-21698G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652490 | |||||||
| chr11:110652709 | A | G | 78 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(75): Show |
79 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.189-21917T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652709 | |||||||
| chr11:110652780 | A | G | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-21988T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652780 | |||||||
| chr11:110652792 | A | G | 89 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(86): Show |
91 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.189-22000T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652792 | |||||||
| chr11:110652847 | G | A | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-22055C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652847 | |||||||
| chr11:110652871 | T | C | 60 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(57): Show |
61 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.189-22079A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652871 | |||||||
| chr11:110652875 | T | C | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-22083A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110652875 | |||||||
| chr11:110653130 | T | G | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-22338A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653130 | |||||||
| chr11:110653178 | G | A | 1 | a0001c0001t0003g0047 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.189-22386C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653178 | |||||||
| chr11:110653208 | G | A | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-22416C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653208 | |||||||
| chr11:110653213 | T | C | 1 | a0001c0002t0005g0208 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.189-22421A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653213 | |||||||
| chr11:110653224 | G | A | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-22432C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653224 | |||||||
| chr11:110653297 | G | A | 3 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 |
4 | HG01891.hp1 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-22505C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653297 | |||||||
| chr11:110653391 | C | T | 1 | a0002c0014t0019g0204 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.189-22599G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653391 | |||||||
| chr11:110653727 | T | TAC | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-22937_189-2293 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653727 | |||||||
| chr11:110653814 | T | C | 77 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(74): Show |
78 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.189-23022A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653814 | |||||||
| chr11:110653914 | A | G | 59 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(56): Show |
60 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.189-23122T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653914 | |||||||
| chr11:110653946 | A | G | 97 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(94): Show |
99 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.189-23154T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653946 | |||||||
| chr11:110653969 | C | T | 5 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-23177G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653969 | |||||||
| chr11:110653971 | A | G | 3 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 |
4 | HG01891.hp1 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-23179T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110653971 | |||||||
| chr11:110654083 | T | C | 1 | a0001c0001t0002g0061 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.189-23291A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110654083 | |||||||
| chr11:110654436 | A | T | 1 | a0003c0004t0002g0142 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.189-23644T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110654436 | |||||||
| chr11:110654472 | A | G | 10 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-23680T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110654472 | |||||||
| chr11:110654487 | A | C | 10 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0004g0006 others(7): Show |
11 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.189-23695T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110654487 | |||||||
| chr11:110654590 | T | C | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-23798A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110654590 | |||||||
| chr11:110654652 | G | C | 5 | a0001c0001t0002g0010 a0001c0001t0006g0154 a0001c0001t0006g0196 others(2): Show |
5 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-23860C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110654652 | |||||||
| chr11:110654670 | C | T | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-23878G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110654670 | |||||||
| chr11:110654902 | G | A | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-24110C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110654902 | |||||||
| chr11:110654958 | C | A | 1 | a0001c0001t0002g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.189-24166G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110654958 | |||||||
| chr11:110655103 | T | G | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-24311A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655103 | |||||||
| chr11:110655104 | A | C | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-24312T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655104 | |||||||
| chr11:110655251 | T | TA | 5 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-24460dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655251 | |||||||
| chr11:110655443 | T | C | 1 | a0001c0001t0011g0020 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.189-24651A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655443 | |||||||
| chr11:110655449 | T | C | 10 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-24657A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655449 | |||||||
| chr11:110655453 | G | A | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-24661C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655453 | |||||||
| chr11:110655610 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0002g0045 a0001c0001t0002g0046 others(1): Show |
4 | HG02080.hp2 NA18989.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-24818C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655610 | |||||||
| chr11:110655644 | G | A | 1 | a0001c0001t0003g0124 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.189-24852C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655644 | |||||||
| chr11:110655666 | G | A | 1 | a0001c0001t0004g0144 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.189-24874C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655666 | |||||||
| chr11:110655700 | G | C | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-24908C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655700 | |||||||
| chr11:110655809 | T | C | 10 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-25017A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655809 | |||||||
| chr11:110655835 | T | C | 2 | a0001c0001t0002g0045 a0001c0001t0002g0046 |
2 | NA18989.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.189-25043A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655835 | |||||||
| chr11:110655959 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.189-25167C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110655959 | |||||||
| chr11:110656029 | C | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0004g0006 others(7): Show |
11 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.189-25237G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656029 | |||||||
| chr11:110656079 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.189-25287C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656079 | |||||||
| chr11:110656107 | T | C | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-25315A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656107 | |||||||
| chr11:110656238 | T | C | 4 | a0001c0001t0001g0039 a0001c0001t0002g0045 a0001c0001t0002g0046 others(1): Show |
4 | HG02080.hp2 NA18989.hp1 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-25446A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656238 | |||||||
| chr11:110656411 | A | G | 60 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(57): Show |
61 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.189-25619T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656411 | |||||||
| chr11:110656455 | G | T | 1 | a0001c0001t0003g0109 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.189-25663C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656455 | |||||||
| chr11:110656500 | C | T | 2 | a0001c0001t0002g0064 a0008c0016t0002g0062 |
2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.189-25708G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656500 | |||||||
| chr11:110656528 | A | G | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-25736T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656528 | |||||||
| chr11:110656531 | A | G | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.189-25739T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656531 | |||||||
| chr11:110656544 | C | A | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189-25752G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656544 | |||||||
| chr11:110656718 | A | G | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-25926T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656718 | |||||||
| chr11:110656776 | T | G | 5 | a0001c0001t0002g0010 a0001c0001t0006g0154 a0001c0001t0006g0196 others(2): Show |
5 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-25984A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656776 | |||||||
| chr11:110656917 | C | T | 1 | a0001c0001t0016g0059 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.189-26125G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110656917 | |||||||
| chr11:110657201 | G | A | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-26409C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657201 | |||||||
| chr11:110657243 | C | A | 1 | a0002c0006t0012g0138 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.189-26451G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657243 | |||||||
| chr11:110657291 | T | G | 1 | a0001c0001t0002g0037 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.189-26499A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657291 | |||||||
| chr11:110657403 | G | A | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.189-26611C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657403 | |||||||
| chr11:110657404 | A | T | 10 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0004g0006 others(7): Show |
11 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.189-26612T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657404 | |||||||
| chr11:110657514 | C | T | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-26722G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657514 | |||||||
| chr11:110657657 | G | A | 2 | a0001c0001t0003g0089 a0001c0013t0003g0068 |
2 | HG03834.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.189-26865C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657657 | |||||||
| chr11:110657752 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.189-26960G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657752 | |||||||
| chr11:110657819 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-27027G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657819 | |||||||
| chr11:110657825 | GC | G | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-27034delG | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657825 | |||||||
| chr11:110657889 | C | T | 1 | a0001c0001t0013g0187 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.189-27097G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657889 | |||||||
| chr11:110657920 | G | GAGGA | 18 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0058 others(15): Show |
18 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.189-27132_189-2712 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657920 | |||||||
| chr11:110657920 | G | GAGGAAGG others(1): Show |
9 | a0001c0001t0001g0049 a0001c0001t0001g0127 a0001c0001t0002g0032 others(6): Show |
10 | HG01891.hp1 HG02622.hp2 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.189-27136_189-2712 others(12): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657920 | |||||||
| chr11:110657920 | G | GAGGAAGG others(5): Show |
2 | a0001c0001t0004g0141 a0002c0006t0012g0138 |
2 | HG03017.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.189-27140_189-2712 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657920 | |||||||
| chr11:110657920 | G | GAGGAAGG others(9): Show |
1 | a0001c0001t0002g0065 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.189-27144_189-2712 others(20): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657920 | |||||||
| chr11:110657920 | GAGGA | G | 28 | a0001c0001t0001g0103 a0001c0001t0001g0130 a0001c0001t0002g0033 others(25): Show |
32 | HG00323.hp1 HG00621.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.189-27132_189-2712 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657920 | |||||||
| chr11:110657920 | GAGGAAGG others(1): Show |
G | 90 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(87): Show |
91 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.189-27136_189-2712 others(12): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657920 | |||||||
| chr11:110657920 | GAGGAAGG others(5): Show |
G | 6 | a0001c0001t0001g0152 a0001c0001t0001g0172 a0001c0001t0001g0188 others(3): Show |
6 | HG02809.hp1 HG02809.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-27140_189-2712 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657920 | |||||||
| chr11:110657946 | G | C | 1 | a0011c0015t0004g0151 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.189-27154C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657946 | |||||||
| chr11:110657949 | A | G | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-27157T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657949 | |||||||
| chr11:110657958 | G | C | 85 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(82): Show |
86 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.189-27166C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110657958 | |||||||
| chr11:110658045 | C | A | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.189-27253G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658045 | |||||||
| chr11:110658246 | A | C | 2 | a0001c0001t0002g0024 a0001c0001t0002g0025 |
2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.189-27454T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658246 | |||||||
| chr11:110658404 | G | A | 5 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-27612C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658404 | |||||||
| chr11:110658443 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.189-27651G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658443 | |||||||
| chr11:110658742 | A | T | 2 | a0001c0001t0002g0024 a0001c0001t0002g0025 |
2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.189-27950T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658742 | |||||||
| chr11:110658780 | A | ATTGTTTT others(3): Show |
63 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(60): Show |
65 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.189-27998_189-2798 others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658780 | |||||||
| chr11:110658780 | A | ATTGTTTT others(8): Show |
17 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0001g0207 others(14): Show |
17 | HG00099.hp2 HG00280.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.189-27989_189-2798 others(19): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658780 | |||||||
| chr11:110658780 | A | ATTGTTTT others(13): Show |
2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-27989_189-2798 others(24): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658780 | |||||||
| chr11:110658932 | C | T | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.189-28140G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658932 | |||||||
| chr11:110658951 | A | G | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.189-28159T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110658951 | |||||||
| chr11:110659009 | G | A | 10 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0004g0095 others(7): Show |
10 | HG00735.hp2 HG01496.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.189-28217C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659009 | |||||||
| chr11:110659094 | C | A | 10 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0004g0006 others(7): Show |
11 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.189-28302G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659094 | |||||||
| chr11:110659119 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.189-28327G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659119 | |||||||
| chr11:110659174 | C | T | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.189-28382G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659174 | |||||||
| chr11:110659188 | T | G | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.189-28396A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659188 | |||||||
| chr11:110659256 | C | G | 8 | a0001c0001t0002g0010 a0001c0001t0006g0154 a0001c0001t0006g0196 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.189-28464G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659256 | |||||||
| chr11:110659307 | C | G | 1 | a0002c0003t0007g0148 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.189-28515G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659307 | |||||||
| chr11:110659396 | T | C | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.189-28604A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659396 | |||||||
| chr11:110659446 | G | A | 1 | a0001c0001t0002g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.189-28654C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659446 | |||||||
| chr11:110659637 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.189-28845A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659637 | |||||||
| chr11:110659717 | C | T | 90 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.189-28925G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659717 | |||||||
| chr11:110659755 | G | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0101 |
2 | NA19057.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.189-28963C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659755 | |||||||
| chr11:110659876 | G | A | 52 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(49): Show |
53 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.189-29084C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659876 | |||||||
| chr11:110659911 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.189-29119C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659911 | |||||||
| chr11:110659918 | T | G | 1 | a0001c0001t0002g0055 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.189-29126A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659918 | |||||||
| chr11:110659922 | G | C | 1 | a0001c0001t0002g0055 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.189-29130C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110659922 | |||||||
| chr11:110660054 | T | TAAAAAAC others(8): Show |
1 | a0012c0017t0002g0139 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.189-29277_189-2926 others(19): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660054 | |||||||
| chr11:110660061 | C | CA | 10 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(7): Show |
10 | HG00323.hp1 HG01099.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-29270dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660061 | |||||||
| chr11:110660061 | CAAAA | C | 7 | a0001c0001t0002g0010 a0001c0001t0006g0154 a0001c0001t0006g0196 others(4): Show |
7 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-29273_189-2927 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660061 | |||||||
| chr11:110660062 | A | AAAAAAAA others(7): Show |
3 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 |
3 | HG00735.hp2 HG01496.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.189-29271_189-2927 others(18): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660062 | |||||||
| chr11:110660063 | A | AAAAAAAA others(4): Show |
2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.189-29272_189-2927 others(15): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660063 | |||||||
| chr11:110660064 | A | AAAAAAAA others(19): Show |
2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.189-29273_189-2927 others(30): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660064 | |||||||
| chr11:110660064 | A | AAAAAAAA others(3): Show |
1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.189-29273_189-2927 others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660064 | |||||||
| chr11:110660064 | A | ACAAAAAA others(5): Show |
52 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(49): Show |
53 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.189-29273_189-2927 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660064 | |||||||
| chr11:110660064 | A | ACAAAAAA others(4): Show |
5 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-29273_189-2927 others(15): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660064 | |||||||
| chr11:110660068 | A | AAAAAAAA others(5): Show |
4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-29277_189-2927 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660068 | |||||||
| chr11:110660069 | A | AAAAAAAC others(5): Show |
9 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(6): Show |
9 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.189-29278_189-2927 others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660069 | |||||||
| chr11:110660069 | A | AAAAAACA others(4): Show |
10 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.189-29278_189-2927 others(15): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660069 | |||||||
| chr11:110660069 | A | C | 57 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(54): Show |
58 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.189-29277T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660069 | |||||||
| chr11:110660212 | G | A | 40 | a0001c0001t0001g0130 a0001c0001t0002g0096 a0001c0001t0003g0001 others(37): Show |
44 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.189-29420C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660212 | |||||||
| chr11:110660717 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.188+29830G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660717 | |||||||
| chr11:110660759 | A | C | 5 | a0001c0001t0002g0093 a0001c0001t0002g0156 a0001c0001t0002g0157 others(2): Show |
5 | HG00673.hp2 HG02040.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+29788T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660759 | |||||||
| chr11:110660785 | C | CT | 5 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+29761dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660785 | |||||||
| chr11:110660828 | G | T | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+29719C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660828 | |||||||
| chr11:110660834 | A | T | 8 | a0001c0001t0002g0010 a0001c0001t0006g0154 a0001c0001t0006g0196 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+29713T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660834 | |||||||
| chr11:110660837 | T | C | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+29710A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660837 | |||||||
| chr11:110660896 | G | T | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+29651C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660896 | |||||||
| chr11:110660959 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.188+29588G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110660959 | |||||||
| chr11:110661024 | A | G | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+29523T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661024 | |||||||
| chr11:110661102 | T | C | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.188+29445A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661102 | |||||||
| chr11:110661117 | A | T | 1 | a0001c0001t0001g0131 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.188+29430T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661117 | |||||||
| chr11:110661208 | A | T | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.188+29339T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661208 | |||||||
| chr11:110661453 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.188+29094G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661453 | |||||||
| chr11:110661460 | C | A | 1 | a0001c0001t0001g0131 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.188+29087G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661460 | |||||||
| chr11:110661573 | AT | A | 10 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.188+28973delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661573 | |||||||
| chr11:110661625 | C | T | 81 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(78): Show |
82 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.188+28922G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661625 | |||||||
| chr11:110661676 | T | C | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+28871A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661676 | |||||||
| chr11:110661740 | T | C | 10 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0004g0006 others(7): Show |
11 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.188+28807A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661740 | |||||||
| chr11:110661993 | G | A | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.188+28554C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110661993 | |||||||
| chr11:110662093 | A | C | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+28454T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110662093 | |||||||
| chr11:110662179 | G | A | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+28368C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110662179 | |||||||
| chr11:110662220 | A | G | 98 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(95): Show |
100 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.188+28327T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110662220 | |||||||
| chr11:110662476 | T | C | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+28071A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110662476 | |||||||
| chr11:110662581 | A | C | 10 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0004g0006 others(7): Show |
11 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.188+27966T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110662581 | |||||||
| chr11:110662658 | C | T | 1 | a0001c0001t0002g0158 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.188+27889G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110662658 | |||||||
| chr11:110663599 | C | T | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+26948G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110663599 | |||||||
| chr11:110663795 | C | A | 1 | a0001c0001t0001g0178 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.188+26752G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110663795 | |||||||
| chr11:110663795 | C | G | 96 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(93): Show |
98 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.188+26752G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110663795 | |||||||
| chr11:110664054 | T | C | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+26493A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664054 | |||||||
| chr11:110664299 | C | T | 7 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(4): Show |
7 | HG02145.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.188+26248G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664299 | |||||||
| chr11:110664349 | C | CAT | 6 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0001t0004g0144 others(3): Show |
7 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+26196_188+2619 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664349 | |||||||
| chr11:110664417 | A | G | 2 | a0001c0009t0002g0185 a0001c0009t0002g0193 |
2 | NA18978.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.188+26130T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664417 | |||||||
| chr11:110664439 | A | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0216 |
3 | HG00099.hp1 HG00741.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.188+26108T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664439 | |||||||
| chr11:110664449 | C | A | 52 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(49): Show |
53 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.188+26098G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664449 | |||||||
| chr11:110664455 | G | A | 7 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(4): Show |
7 | HG02145.hp2 HG02451.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.188+26092C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664455 | |||||||
| chr11:110664491 | G | A | 8 | a0001c0001t0002g0010 a0001c0001t0006g0154 a0001c0001t0006g0196 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+26056C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664491 | |||||||
| chr11:110664615 | C | G | 5 | a0001c0001t0002g0061 a0001c0001t0002g0063 a0001c0001t0002g0064 others(2): Show |
5 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+25932G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664615 | |||||||
| chr11:110664644 | C | T | 60 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(57): Show |
61 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.188+25903G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664644 | |||||||
| chr11:110664706 | C | T | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+25841G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664706 | |||||||
| chr11:110664727 | C | CA | 8 | a0001c0001t0001g0088 a0001c0001t0001g0114 a0001c0001t0002g0036 others(5): Show |
8 | HG00733.hp1 HG01169.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+25819dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664727 | |||||||
| chr11:110664727 | CA | C | 10 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0004g0006 others(7): Show |
11 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.188+25819delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664727 | |||||||
| chr11:110664727 | CAA | C | 80 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(77): Show |
81 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.188+25818_188+2581 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664727 | |||||||
| chr11:110664727 | CAAAAAAA | C | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+25813_188+2581 others(11): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664727 | |||||||
| chr11:110664727 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0073 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.188+25810_188+2581 others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664727 | |||||||
| chr11:110664774 | C | T | 5 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+25773G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664774 | |||||||
| chr11:110664820 | T | C | 1 | a0001c0001t0003g0109 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.188+25727A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110664820 | |||||||
| chr11:110665145 | G | A | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+25402C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665145 | |||||||
| chr11:110665156 | C | A | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+25391G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665156 | |||||||
| chr11:110665244 | A | G | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.188+25303T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665244 | |||||||
| chr11:110665373 | C | T | 2 | a0001c0001t0003g0092 a0001c0001t0003g0102 |
2 | HG01346.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.188+25174G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665373 | |||||||
| chr11:110665617 | G | A | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+24930C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665617 | |||||||
| chr11:110665628 | A | G | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+24919T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665628 | |||||||
| chr11:110665813 | T | C | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+24734A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665813 | |||||||
| chr11:110665835 | A | G | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+24712T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665835 | |||||||
| chr11:110665905 | A | T | 1 | a0002c0006t0012g0138 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.188+24642T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665905 | |||||||
| chr11:110665970 | TAC | T | 88 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(85): Show |
90 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.188+24575_188+2457 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665970 | |||||||
| chr11:110665972 | C | T | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+24575G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665972 | |||||||
| chr11:110665976 | TACAC | T | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+24567_188+2457 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665976 | |||||||
| chr11:110665978 | C | T | 87 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(84): Show |
89 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.188+24569G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110665978 | |||||||
| chr11:110666011 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.188+24536C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666011 | |||||||
| chr11:110666048 | T | C | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+24499A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666048 | |||||||
| chr11:110666177 | T | C | 8 | a0001c0001t0002g0010 a0001c0001t0006g0154 a0001c0001t0006g0196 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+24370A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666177 | |||||||
| chr11:110666273 | T | C | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+24274A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666273 | |||||||
| chr11:110666409 | G | A | 90 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.188+24138C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666409 | |||||||
| chr11:110666544 | G | A | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+24003C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666544 | |||||||
| chr11:110666571 | T | C | 97 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(94): Show |
99 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.188+23976A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666571 | |||||||
| chr11:110666596 | A | T | 1 | a0001c0001t0002g0071 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.188+23951T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666596 | |||||||
| chr11:110666639 | C | A | 5 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+23908G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666639 | |||||||
| chr11:110666784 | C | T | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+23763G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666784 | |||||||
| chr11:110666834 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+23713G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666834 | |||||||
| chr11:110666849 | T | G | 2 | a0001c0001t0002g0061 a0001c0001t0002g0063 |
2 | HG02109.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.188+23698A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666849 | |||||||
| chr11:110666866 | G | C | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+23681C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110666866 | |||||||
| chr11:110667054 | A | G | 1 | a0001c0001t0002g0098 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.188+23493T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110667054 | |||||||
| chr11:110667365 | T | C | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+23182A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110667365 | |||||||
| chr11:110667557 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.188+22990C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110667557 | |||||||
| chr11:110667566 | A | C | 85 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(82): Show |
86 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.188+22981T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110667566 | |||||||
| chr11:110667614 | A | C | 4 | a0001c0001t0003g0209 a0001c0002t0005g0208 a0001c0002t0005g0214 others(1): Show |
4 | HG02015.hp1 HG02080.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+22933T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110667614 | |||||||
| chr11:110667703 | T | C | 8 | a0001c0001t0002g0010 a0001c0001t0006g0154 a0001c0001t0006g0196 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+22844A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110667703 | |||||||
| chr11:110668008 | G | A | 1 | a0001c0001t0003g0089 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.188+22539C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110668008 | |||||||
| chr11:110668101 | A | G | 6 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(3): Show |
7 | HG01891.hp1 HG02622.hp2 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+22446T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110668101 | |||||||
| chr11:110668374 | G | A | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0013g0110 others(1): Show |
4 | HG02015.hp2 NA18940.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+22173C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110668374 | |||||||
| chr11:110668467 | G | A | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+22080C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110668467 | |||||||
| chr11:110668666 | AAAAGAAA others(2): Show |
A | 8 | a0001c0001t0002g0010 a0001c0001t0006g0154 a0001c0001t0006g0196 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+21872_188+2188 others(13): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110668666 | |||||||
| chr11:110668720 | A | G | 3 | a0001c0001t0002g0156 a0001c0001t0002g0157 a0001c0012t0002g0186 |
3 | HG02040.hp1 NA18951.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.188+21827T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110668720 | |||||||
| chr11:110668785 | T | A | 1 | a0001c0001t0001g0165 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.188+21762A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110668785 | |||||||
| chr11:110669098 | A | G | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188+21449T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669098 | |||||||
| chr11:110669117 | A | C | 8 | a0001c0001t0002g0010 a0001c0001t0006g0154 a0001c0001t0006g0196 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+21430T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669117 | |||||||
| chr11:110669285 | C | T | 10 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.188+21262G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669285 | |||||||
| chr11:110669411 | C | G | 8 | a0001c0001t0002g0010 a0001c0001t0006g0154 a0001c0001t0006g0196 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+21136G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669411 | |||||||
| chr11:110669418 | T | C | 77 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(74): Show |
78 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.188+21129A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669418 | |||||||
| chr11:110669483 | C | A | 1 | a0001c0001t0001g0165 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.188+21064G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669483 | |||||||
| chr11:110669510 | T | C | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+21037A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669510 | |||||||
| chr11:110669573 | A | G | 60 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(57): Show |
61 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.188+20974T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669573 | |||||||
| chr11:110669632 | A | G | 8 | a0001c0001t0002g0010 a0001c0001t0006g0154 a0001c0001t0006g0196 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+20915T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669632 | |||||||
| chr11:110669818 | T | C | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+20729A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669818 | |||||||
| chr11:110669904 | A | G | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+20643T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110669904 | |||||||
| chr11:110670032 | C | A | 1 | a0002c0014t0019g0204 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.188+20515G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670032 | |||||||
| chr11:110670218 | C | T | 1 | a0001c0001t0003g0210 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.188+20329G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670218 | |||||||
| chr11:110670329 | AC | A | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188+20217delG | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670329 | |||||||
| chr11:110670331 | T | A | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188+20216A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670331 | |||||||
| chr11:110670506 | G | A | 8 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0001t0004g0144 others(5): Show |
9 | HG01891.hp1 HG02622.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.188+20041C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670506 | |||||||
| chr11:110670574 | A | G | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.188+19973T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670574 | |||||||
| chr11:110670655 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.188+19892G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670655 | |||||||
| chr11:110670858 | G | A | 10 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(7): Show |
10 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.188+19689C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670858 | |||||||
| chr11:110670914 | G | T | 1 | a0002c0014t0019g0204 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.188+19633C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110670914 | |||||||
| chr11:110671025 | T | G | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 |
3 | HG00280.hp1 HG01074.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.188+19522A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671025 | |||||||
| chr11:110671229 | G | GA | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+19317dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671229 | |||||||
| chr11:110671244 | C | T | 69 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(66): Show |
70 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.188+19303G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671244 | |||||||
| chr11:110671396 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0003g0090 |
2 | HG02602.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.188+19151A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671396 | |||||||
| chr11:110671403 | T | C | 5 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+19144A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671403 | |||||||
| chr11:110671415 | G | T | 1 | a0001c0001t0002g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.188+19132C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671415 | |||||||
| chr11:110671417 | A | G | 1 | a0001c0001t0002g0162 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.188+19130T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671417 | |||||||
| chr11:110671509 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+19038G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671509 | |||||||
| chr11:110671519 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.188+19028T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671519 | |||||||
| chr11:110671539 | T | C | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+19008A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671539 | |||||||
| chr11:110671642 | A | C | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188+18905T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671642 | |||||||
| chr11:110671865 | G | T | 1 | a0001c0001t0004g0095 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.188+18682C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110671865 | |||||||
| chr11:110672437 | C | A | 1 | a0001c0002t0005g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.188+18110G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110672437 | |||||||
| chr11:110672474 | AT | A | 8 | a0001c0001t0002g0010 a0001c0001t0006g0154 a0001c0001t0006g0196 others(5): Show |
8 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+18072delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110672474 | |||||||
| chr11:110672606 | G | A | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188+17941C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110672606 | |||||||
| chr11:110672797 | C | T | 70 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(67): Show |
71 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.188+17750G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110672797 | |||||||
| chr11:110672893 | G | C | 18 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0002g0010 others(15): Show |
19 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.188+17654C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110672893 | |||||||
| chr11:110672928 | G | A | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+17619C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110672928 | |||||||
| chr11:110673075 | T | A | 2 | a0001c0001t0003g0092 a0001c0001t0003g0102 |
2 | HG01346.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.188+17472A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673075 | |||||||
| chr11:110673109 | A | T | 4 | a0001c0001t0008g0016 a0001c0001t0008g0017 a0001c0001t0008g0021 others(1): Show |
4 | NA18997.hp1 NA19003.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+17438T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673109 | |||||||
| chr11:110673182 | A | G | 70 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(67): Show |
71 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.188+17365T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673182 | |||||||
| chr11:110673373 | T | C | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.188+17174A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673373 | |||||||
| chr11:110673477 | C | T | 1 | a0013c0019t0004g0149 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.188+17070G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673477 | |||||||
| chr11:110673725 | G | A | 1 | a0001c0001t0006g0171 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.188+16822C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673725 | |||||||
| chr11:110673934 | G | T | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+16613C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673934 | |||||||
| chr11:110673941 | A | AT | 6 | a0001c0001t0001g0105 a0001c0001t0003g0104 a0001c0001t0011g0020 others(3): Show |
6 | HG02622.hp2 HG03540.hp2 NA18972.hp1 others(3): Show |
intron_variant | MODIFIER | c.188+16605dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673941 | |||||||
| chr11:110673941 | AT | A | 73 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(70): Show |
74 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.188+16605delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673941 | |||||||
| chr11:110673941 | ATTT | A | 5 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0013 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+16603_188+1660 others(7): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673941 | |||||||
| chr11:110673964 | C | T | 1 | a0002c0003t0007g0148 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.188+16583G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110673964 | |||||||
| chr11:110674102 | C | G | 52 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(49): Show |
53 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.188+16445G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674102 | |||||||
| chr11:110674147 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | HG00280.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.188+16400C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674147 | |||||||
| chr11:110674160 | T | C | 2 | a0001c0001t0002g0010 a0001c0001t0006g0154 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.188+16387A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674160 | |||||||
| chr11:110674234 | A | G | 97 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(94): Show |
99 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.188+16313T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674234 | |||||||
| chr11:110674282 | A | G | 2 | a0001c0001t0002g0200 a0002c0003t0007g0199 |
2 | HG01074.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.188+16265T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674282 | |||||||
| chr11:110674630 | T | TTA | 5 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(2): Show |
5 | HG00735.hp2 HG01496.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+15915_188+1591 others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674630 | |||||||
| chr11:110674734 | T | C | 79 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(76): Show |
80 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.188+15813A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674734 | |||||||
| chr11:110674758 | C | G | 4 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0003c0004t0002g0142 others(1): Show |
4 | HG00735.hp2 HG01496.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+15789G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674758 | |||||||
| chr11:110674775 | T | G | 59 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0027 others(56): Show |
60 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.188+15772A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674775 | |||||||
| chr11:110674807 | T | C | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+15740A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674807 | |||||||
| chr11:110674977 | T | C | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+15570A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110674977 | |||||||
| chr11:110675270 | C | T | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+15277G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110675270 | |||||||
| chr11:110675347 | C | T | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188+15200G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110675347 | |||||||
| chr11:110675479 | A | T | 4 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 others(1): Show |
5 | HG01891.hp1 HG03017.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+15068T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110675479 | |||||||
| chr11:110675490 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.188+15057C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110675490 | |||||||
| chr11:110675573 | A | G | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.188+14974T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110675573 | |||||||
| chr11:110675656 | C | T | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+14891G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110675656 | |||||||
| chr11:110675675 | C | T | 1 | a0001c0001t0003g0129 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.188+14872G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110675675 | |||||||
| chr11:110675904 | A | T | 9 | a0001c0001t0001g0029 a0001c0001t0001g0137 a0001c0001t0004g0006 others(6): Show |
10 | HG00735.hp2 HG01496.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.188+14643T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110675904 | |||||||
| chr11:110676202 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0137 |
2 | HG00735.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.188+14345A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676202 | |||||||
| chr11:110676303 | T | C | 1 | a0003c0004t0002g0160 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.188+14244A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676303 | |||||||
| chr11:110676382 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.188+14165C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676382 | |||||||
| chr11:110676427 | C | T | 1 | a0001c0001t0008g0016 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.188+14120G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676427 | |||||||
| chr11:110676431 | C | G | 1 | a0002c0006t0012g0138 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.188+14116G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676431 | |||||||
| chr11:110676453 | G | A | 6 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+14094C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676453 | |||||||
| chr11:110676523 | A | T | 11 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0003g0210 others(8): Show |
11 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.188+14024T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676523 | |||||||
| chr11:110676563 | G | A | 3 | a0001c0001t0001g0137 a0003c0004t0002g0142 a0012c0017t0002g0139 |
3 | HG00735.hp2 HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.188+13984C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676563 | |||||||
| chr11:110676588 | T | G | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.188+13959A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676588 | |||||||
| chr11:110676817 | G | GT | 31 | a0001c0001t0001g0192 a0001c0001t0001g0207 a0001c0001t0002g0010 others(28): Show |
32 | HG00099.hp2 HG00280.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.188+13729dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676817 | |||||||
| chr11:110676827 | T | A | 5 | a0001c0001t0001g0137 a0001c0001t0002g0098 a0002c0006t0012g0138 others(2): Show |
5 | HG00735.hp2 HG03017.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.188+13720A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676827 | |||||||
| chr11:110676828 | A | T | 65 | a0001c0001t0001g0022 a0001c0001t0001g0027 a0001c0001t0001g0134 others(62): Show |
65 | HG00280.hp2 HG00621.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.188+13719T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676828 | |||||||
| chr11:110676829 | A | T | 1 | a0001c0001t0001g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.188+13718T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676829 | |||||||
| chr11:110676981 | T | C | 1 | a0001c0001t0002g0096 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.188+13566A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110676981 | |||||||
| chr11:110677036 | C | T | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+13511G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110677036 | |||||||
| chr11:110677112 | A | C | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.188+13435T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110677112 | |||||||
| chr11:110677113 | G | C | 1 | a0011c0015t0004g0151 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.188+13434C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110677113 | |||||||
| chr11:110677387 | C | G | 12 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0003g0210 others(9): Show |
12 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.188+13160G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110677387 | |||||||
| chr11:110677647 | GA | G | 22 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0003g0209 others(19): Show |
22 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.188+12899delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110677647 | |||||||
| chr11:110677735 | G | A | 48 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(45): Show |
49 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.188+12812C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110677735 | |||||||
| chr11:110677848 | C | T | 2 | a0001c0001t0001g0131 a0001c0005t0005g0194 |
2 | HG02451.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.188+12699G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110677848 | |||||||
| chr11:110678062 | A | G | 35 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0200 others(32): Show |
35 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.188+12485T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110678062 | |||||||
| chr11:110678085 | T | C | 3 | a0001c0001t0006g0196 a0001c0001t0006g0197 a0001c0001t0006g0198 |
3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.188+12462A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110678085 | |||||||
| chr11:110678357 | A | G | 9 | a0001c0001t0002g0028 a0001c0001t0002g0031 a0001c0001t0002g0033 others(6): Show |
9 | HG01109.hp2 HG02486.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.188+12190T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110678357 | |||||||
| chr11:110678509 | G | T | 8 | a0001c0001t0002g0010 a0001c0001t0004g0011 a0001c0001t0004g0012 others(5): Show |
8 | HG02145.hp2 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+12038C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110678509 | |||||||
| chr11:110678545 | G | A | 1 | a0001c0001t0002g0064 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.188+12002C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110678545 | |||||||
| chr11:110678597 | T | C | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+11950A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110678597 | |||||||
| chr11:110678755 | A | G | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188+11792T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110678755 | |||||||
| chr11:110678807 | C | G | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.188+11740G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110678807 | |||||||
| chr11:110678896 | C | T | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.188+11651G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110678896 | |||||||
| chr11:110679288 | C | T | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+11259G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110679288 | |||||||
| chr11:110679348 | G | C | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.188+11199C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110679348 | |||||||
| chr11:110679656 | T | C | 12 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0003g0210 others(9): Show |
12 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.188+10891A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110679656 | |||||||
| chr11:110679670 | T | C | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+10877A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110679670 | |||||||
| chr11:110679903 | C | A | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.188+10644G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110679903 | |||||||
| chr11:110679915 | T | C | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.188+10632A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110679915 | |||||||
| chr11:110679943 | G | A | 3 | a0001c0001t0006g0196 a0001c0001t0006g0197 a0001c0001t0006g0198 |
3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.188+10604C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110679943 | |||||||
| chr11:110680152 | A | T | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.188+10395T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110680152 | |||||||
| chr11:110680214 | G | A | 1 | a0013c0019t0004g0149 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.188+10333C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110680214 | |||||||
| chr11:110680590 | T | G | 2 | a0001c0009t0002g0185 a0001c0009t0002g0193 |
2 | NA18978.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.188+9957A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110680590 | |||||||
| chr11:110680883 | A | C | 1 | a0001c0001t0002g0200 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.188+9664T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110680883 | |||||||
| chr11:110680887 | T | C | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+9660A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110680887 | |||||||
| chr11:110680942 | T | C | 47 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(44): Show |
48 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.188+9605A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110680942 | |||||||
| chr11:110681048 | T | C | 4 | a0001c0001t0003g0209 a0001c0002t0005g0208 a0001c0002t0005g0214 others(1): Show |
4 | HG02015.hp1 HG02080.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+9499A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110681048 | |||||||
| chr11:110681049 | G | A | 10 | a0001c0001t0002g0010 a0001c0001t0004g0011 a0001c0001t0004g0012 others(7): Show |
10 | HG02145.hp2 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.188+9498C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110681049 | |||||||
| chr11:110681143 | G | A | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.188+9404C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110681143 | |||||||
| chr11:110681274 | G | T | 5 | a0001c0001t0002g0010 a0001c0001t0004g0011 a0001c0001t0004g0012 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+9273C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110681274 | |||||||
| chr11:110681398 | T | C | 2 | a0001c0001t0002g0065 a0001c0001t0002g0112 |
2 | HG01192.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.188+9149A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110681398 | |||||||
| chr11:110681549 | T | G | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+8998A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110681549 | |||||||
| chr11:110681666 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.188+8881A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110681666 | |||||||
| chr11:110681729 | G | C | 4 | a0001c0001t0001g0027 a0001c0001t0002g0042 a0001c0001t0002g0043 others(1): Show |
4 | NA18940.hp2 NA18953.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+8818C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110681729 | |||||||
| chr11:110682052 | T | G | 44 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(41): Show |
45 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.188+8495A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110682052 | |||||||
| chr11:110682278 | A | G | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188+8269T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110682278 | |||||||
| chr11:110682302 | A | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0216 |
3 | HG00099.hp1 HG00741.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.188+8245T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110682302 | |||||||
| chr11:110682448 | A | G | 6 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+8099T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110682448 | |||||||
| chr11:110682483 | A | T | 2 | a0001c0001t0003g0001 a0001c0001t0003g0051 |
4 | HG01928.hp2 HG01981.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+8064T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110682483 | |||||||
| chr11:110682715 | T | C | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+7832A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110682715 | |||||||
| chr11:110682863 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.188+7684C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110682863 | |||||||
| chr11:110682957 | A | G | 3 | a0001c0001t0001g0105 a0001c0001t0011g0018 a0001c0001t0011g0020 |
3 | HG02155.hp1 NA18972.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.188+7590T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110682957 | |||||||
| chr11:110682999 | T | TA | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.188+7547dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110682999 | |||||||
| chr11:110683744 | T | C | 6 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+6803A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110683744 | |||||||
| chr11:110683778 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.188+6769A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110683778 | |||||||
| chr11:110683793 | C | T | 10 | a0001c0001t0001g0137 a0001c0001t0002g0162 a0001c0001t0002g0163 others(7): Show |
11 | HG00735.hp2 HG01891.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.188+6754G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110683793 | |||||||
| chr11:110683923 | T | C | 6 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+6624A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110683923 | |||||||
| chr11:110684035 | C | G | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.188+6512G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684035 | |||||||
| chr11:110684092 | A | G | 1 | a0001c0001t0003g0104 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.188+6455T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684092 | |||||||
| chr11:110684125 | T | C | 8 | a0001c0001t0002g0010 a0001c0001t0004g0011 a0001c0001t0004g0012 others(5): Show |
8 | HG02145.hp2 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+6422A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684125 | |||||||
| chr11:110684164 | G | GT | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+6382dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684164 | |||||||
| chr11:110684231 | A | T | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.188+6316T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684231 | |||||||
| chr11:110684234 | A | C | 6 | a0001c0001t0001g0130 a0001c0001t0003g0056 a0001c0001t0003g0066 others(3): Show |
6 | HG00323.hp1 HG01099.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+6313T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684234 | |||||||
| chr11:110684266 | T | A | 1 | a0005c0007t0010g0146 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.188+6281A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684266 | |||||||
| chr11:110684287 | G | A | 29 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0200 others(26): Show |
29 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.188+6260C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684287 | |||||||
| chr11:110684403 | T | A | 1 | a0001c0001t0001g0155 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.188+6144A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684403 | |||||||
| chr11:110684483 | G | T | 1 | a0001c0001t0001g0060 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.188+6064C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684483 | |||||||
| chr11:110684872 | G | GGGAACAC others(2): Show |
90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.188+5674_188+5675i others(11): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110684872 | |||||||
| chr11:110685131 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.188+5416A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685131 | |||||||
| chr11:110685138 | T | A | 1 | a0001c0001t0003g0015 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.188+5409A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685138 | |||||||
| chr11:110685197 | T | TAGA | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.188+5347_188+5349d others(5): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685197 | |||||||
| chr11:110685216 | A | G | 12 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0003g0210 others(9): Show |
12 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.188+5331T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685216 | |||||||
| chr11:110685422 | A | T | 1 | a0008c0016t0002g0062 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.188+5125T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685422 | |||||||
| chr11:110685494 | T | TA | 80 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(77): Show |
82 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.188+5052dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685494 | |||||||
| chr11:110685494 | T | TAA | 10 | a0001c0001t0002g0010 a0001c0001t0004g0011 a0001c0001t0004g0012 others(7): Show |
10 | HG02145.hp2 HG02622.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.188+5051_188+5052d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685494 | |||||||
| chr11:110685560 | T | C | 48 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(45): Show |
49 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.188+4987A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685560 | |||||||
| chr11:110685587 | AAT | A | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+4958_188+4959d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685587 | |||||||
| chr11:110685617 | A | C | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.188+4930T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685617 | |||||||
| chr11:110685702 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.188+4845C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685702 | |||||||
| chr11:110685759 | G | A | 35 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0200 others(32): Show |
35 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.188+4788C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685759 | |||||||
| chr11:110685936 | C | CG | 6 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+4610dupC | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685936 | |||||||
| chr11:110685953 | A | G | 11 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0003g0210 others(8): Show |
11 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.188+4594T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685953 | |||||||
| chr11:110685972 | C | A | 83 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(80): Show |
85 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.188+4575G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110685972 | |||||||
| chr11:110686127 | T | C | 2 | a0004c0010t0001g0159 a0004c0010t0001g0179 |
2 | HG01981.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.188+4420A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686127 | |||||||
| chr11:110686446 | A | C | 6 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+4101T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686446 | |||||||
| chr11:110686494 | C | T | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.188+4053G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686494 | |||||||
| chr11:110686561 | C | A | 12 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0003g0210 others(9): Show |
12 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.188+3986G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686561 | |||||||
| chr11:110686652 | C | T | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+3895G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686652 | |||||||
| chr11:110686699 | T | C | 11 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0003g0210 others(8): Show |
11 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.188+3848A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686699 | |||||||
| chr11:110686724 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.188+3823T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686724 | |||||||
| chr11:110686759 | T | G | 2 | a0001c0001t0008g0016 a0001c0001t0008g0021 |
2 | NA18997.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.188+3788A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686759 | |||||||
| chr11:110686829 | C | T | 6 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+3718G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686829 | |||||||
| chr11:110686943 | A | G | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+3604T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110686943 | |||||||
| chr11:110687010 | G | C | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.188+3537C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687010 | |||||||
| chr11:110687035 | C | CAT | 8 | a0001c0001t0001g0049 a0001c0001t0001g0192 a0001c0001t0002g0024 others(5): Show |
8 | HG00558.hp2 HG02809.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+3510_188+3511d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687035 | C | CATAT | 3 | a0001c0001t0001g0007 a0001c0001t0001g0172 a0001c0001t0001g0190 |
4 | HG02622.hp1 HG03041.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+3508_188+3511d others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687035 | C | CATATATA others(1): Show |
3 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 |
4 | HG01891.hp1 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+3504_188+3511d others(10): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687035 | C | CATATATA others(3): Show |
4 | a0001c0001t0002g0158 a0001c0005t0005g0194 a0003c0004t0002g0142 others(1): Show |
4 | HG00673.hp2 HG02451.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+3502_188+3511d others(12): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687035 | C | CATATATA others(5): Show |
4 | a0001c0001t0001g0153 a0001c0001t0004g0013 a0001c0001t0006g0171 others(1): Show |
4 | HG01361.hp1 HG02280.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+3500_188+3511d others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687035 | C | CATATATA others(7): Show |
5 | a0001c0001t0002g0010 a0001c0001t0004g0011 a0001c0001t0004g0012 others(2): Show |
5 | HG02109.hp1 HG02145.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.188+3498_188+3511d others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687035 | C | CATATATA others(9): Show |
4 | a0001c0001t0001g0207 a0001c0001t0006g0197 a0001c0001t0006g0198 others(1): Show |
4 | HG00099.hp2 HG02257.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+3496_188+3511d others(18): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687035 | C | CATATATA others(11): Show |
5 | a0001c0002t0005g0212 a0001c0002t0005g0213 a0001c0002t0005g0214 others(2): Show |
5 | HG02015.hp1 HG02080.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.188+3494_188+3511d others(20): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687035 | C | CATATATA others(13): Show |
8 | a0001c0001t0001g0137 a0001c0001t0001g0170 a0001c0001t0001g0180 others(5): Show |
8 | HG00621.hp1 HG00735.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+3492_188+3511d others(22): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687035 | C | CATATATA others(15): Show |
9 | a0001c0001t0001g0169 a0001c0001t0001g0188 a0001c0001t0002g0202 others(6): Show |
9 | HG02922.hp1 HG03139.hp2 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.188+3511_188+3512i others(24): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687035 | C | CATATATA others(17): Show |
8 | a0001c0001t0001g0134 a0001c0001t0001g0167 a0001c0001t0001g0168 others(5): Show |
8 | HG00733.hp2 HG01169.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.188+3511_188+3512i others(26): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687035 | C | CATATATA others(19): Show |
8 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0002g0162 others(5): Show |
8 | HG02071.hp2 HG02132.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.188+3511_188+3512i others(28): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687035 | C | CATATATA others(21): Show |
1 | a0001c0012t0002g0186 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.188+3511_188+3512i others(30): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687035 | C | CATATATA others(23): Show |
5 | a0001c0001t0001g0150 a0001c0001t0002g0156 a0001c0001t0002g0157 others(2): Show |
5 | HG01074.hp1 HG01891.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.188+3511_188+3512i others(32): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687035 | C | CATATATA others(25): Show |
7 | a0001c0001t0001g0152 a0001c0001t0001g0155 a0001c0001t0001g0161 others(4): Show |
7 | HG01433.hp2 HG02155.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+3511_188+3512i others(34): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687035 | C | CATATATA others(27): Show |
1 | a0001c0001t0001g0135 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.188+3511_188+3512i others(36): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687035 | C | CATATATA others(35): Show |
1 | a0003c0004t0002g0160 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.188+3511_188+3512i others(44): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687035 | CAT | C | 3 | a0001c0001t0002g0098 a0001c0001t0002g0125 a0001c0001t0008g0016 |
3 | HG01516.hp1 NA18997.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.188+3510_188+3511d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687035 | CATAT | C | 8 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(5): Show |
8 | HG00639.hp2 HG01981.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.188+3508_188+3511d others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687035 | |||||||
| chr11:110687055 | T | TATATATA others(7): Show |
1 | a0013c0019t0004g0149 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.188+3491_188+3492i others(16): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687055 | |||||||
| chr11:110687057 | G | C | 1 | a0013c0019t0004g0149 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.188+3490C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687057 | |||||||
| chr11:110687057 | G | GAC | 6 | a0001c0001t0001g0060 a0001c0001t0001g0101 a0001c0001t0003g0133 others(3): Show |
6 | HG01358.hp1 HG02015.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+3488_188+3489d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687057 | |||||||
| chr11:110687057 | G | T | 68 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(65): Show |
69 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.188+3490C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687057 | |||||||
| chr11:110687057 | GAC | G | 2 | a0001c0001t0002g0061 a0001c0001t0003g0121 |
2 | HG03139.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.188+3488_188+3489d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687057 | |||||||
| chr11:110687059 | C | G | 68 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(65): Show |
69 | HG00099.hp2 HG00621.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.188+3488G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687059 | |||||||
| chr11:110687061 | CACACACA others(19): Show |
C | 1 | a0001c0001t0003g0102 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.188+3460_188+3485d others(28): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687061 | |||||||
| chr11:110687077 | C | T | 12 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(9): Show |
12 | HG00280.hp2 HG00639.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.188+3470G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687077 | |||||||
| chr11:110687083 | T | TAGAC | 8 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG00639.hp2 HG01981.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.188+3463_188+3464i others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687083 | |||||||
| chr11:110687083 | T | TAGACAC | 2 | a0001c0001t0001g0174 a0001c0005t0005g0194 |
2 | HG02451.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.188+3463_188+3464i others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687083 | |||||||
| chr11:110687083 | T | TAGACACA others(1): Show |
2 | a0001c0002t0005g0206 a0010c0020t0020g0147 |
2 | HG00280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.188+3463_188+3464i others(10): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687083 | |||||||
| chr11:110687085 | T | C | 12 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(9): Show |
12 | HG00280.hp2 HG00639.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.188+3462A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687085 | |||||||
| chr11:110687087 | G | C | 12 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0175 others(9): Show |
12 | HG00280.hp2 HG00639.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.188+3460C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687087 | |||||||
| chr11:110687087 | G | GAC | 4 | a0001c0001t0001g0094 a0001c0001t0003g0003 a0001c0001t0006g0197 others(1): Show |
4 | HG02486.hp2 NA19084.hp2 NA19091.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+3458_188+3459d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687087 | |||||||
| chr11:110687087 | G | GACAC | 46 | a0001c0001t0001g0022 a0001c0001t0001g0105 a0001c0001t0001g0127 others(43): Show |
50 | HG00323.hp1 HG00621.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.188+3456_188+3459d others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687087 | |||||||
| chr11:110687087 | G | GACACAC | 49 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(46): Show |
50 | HG00621.hp1 HG00673.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.188+3454_188+3459d others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687087 | |||||||
| chr11:110687087 | G | GACACACA others(1): Show |
6 | a0001c0001t0001g0168 a0001c0001t0004g0144 a0003c0004t0017g0143 others(3): Show |
6 | HG02622.hp2 HG02809.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+3452_188+3459d others(10): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687087 | |||||||
| chr11:110687087 | G | GACACACA others(3): Show |
9 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0003g0210 others(6): Show |
9 | HG00099.hp2 HG02145.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.188+3450_188+3459d others(12): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687087 | |||||||
| chr11:110687087 | G | GACACACA others(5): Show |
6 | a0001c0001t0003g0209 a0001c0001t0004g0011 a0001c0001t0004g0012 others(3): Show |
6 | HG02015.hp1 HG02080.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+3448_188+3459d others(14): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687087 | |||||||
| chr11:110687139 | A | G | 47 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(44): Show |
48 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.188+3408T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687139 | |||||||
| chr11:110687472 | G | A | 55 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(52): Show |
57 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.188+3075C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687472 | |||||||
| chr11:110687574 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.188+2973C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687574 | |||||||
| chr11:110687707 | A | C | 1 | a0001c0002t0005g0208 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.188+2840T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110687707 | |||||||
| chr11:110688013 | T | C | 3 | a0001c0001t0001g0137 a0003c0004t0002g0142 a0012c0017t0002g0139 |
3 | HG00735.hp2 HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.188+2534A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688013 | |||||||
| chr11:110688063 | T | C | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+2484A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688063 | |||||||
| chr11:110688090 | C | G | 28 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0003g0209 others(25): Show |
28 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.188+2457G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688090 | |||||||
| chr11:110688095 | G | A | 1 | a0001c0001t0003g0121 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.188+2452C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688095 | |||||||
| chr11:110688282 | C | G | 1 | a0001c0001t0003g0067 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.188+2265G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688282 | |||||||
| chr11:110688775 | T | C | 1 | a0001c0001t0004g0013 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.188+1772A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688775 | |||||||
| chr11:110688792 | G | T | 1 | a0002c0003t0007g0199 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.188+1755C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688792 | |||||||
| chr11:110688895 | T | C | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+1652A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688895 | |||||||
| chr11:110688999 | G | GC | 11 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0003g0210 others(8): Show |
11 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.188+1547_188+1548i others(3): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688999 | |||||||
| chr11:110688999 | G | GT | 27 | a0001c0001t0001g0216 a0001c0001t0002g0010 a0001c0001t0002g0055 others(24): Show |
27 | HG00741.hp2 HG01074.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.188+1547dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688999 | |||||||
| chr11:110688999 | G | GTT | 52 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0150 others(49): Show |
54 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.188+1546_188+1547d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110688999 | |||||||
| chr11:110689000 | T | C | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+1547A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689000 | |||||||
| chr11:110689092 | C | G | 1 | a0001c0001t0009g0118 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.188+1455G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689092 | |||||||
| chr11:110689159 | C | T | 47 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(44): Show |
48 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.188+1388G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689159 | |||||||
| chr11:110689236 | C | T | 1 | a0004c0010t0001g0159 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.188+1311G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689236 | |||||||
| chr11:110689521 | ATAAAT | A | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.188+1021_188+1025d others(7): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689521 | |||||||
| chr11:110689682 | T | C | 11 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0003g0210 others(8): Show |
11 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.188+865A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689682 | |||||||
| chr11:110689740 | CGGGGAAA others(17): Show |
C | 7 | a0001c0001t0002g0010 a0001c0001t0004g0011 a0001c0001t0004g0012 others(4): Show |
7 | HG02145.hp2 HG02647.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.188+783_188+806del others(24): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689740 | |||||||
| chr11:110689856 | C | T | 2 | a0001c0001t0002g0026 a0001c0001t0002g0032 |
2 | HG03491.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.188+691G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689856 | |||||||
| chr11:110689869 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.188+678A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689869 | |||||||
| chr11:110689961 | C | CA | 57 | a0001c0001t0001g0007 a0001c0001t0001g0105 a0001c0001t0001g0134 others(54): Show |
58 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.188+585dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689961 | |||||||
| chr11:110689994 | T | C | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.188+553A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110689994 | |||||||
| chr11:110690190 | C | A | 1 | a0001c0001t0001g0216 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.188+357G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110690190 | |||||||
| chr11:110690453 | C | T | 11 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0003g0210 others(8): Show |
11 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.188+94G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | 110690453 | |||||||
| chr11:110690707 | T | G | 1 | a0001c0001t0001g0191 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.106-78A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110690707 | |||||||
| chr11:110690738 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.106-109C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110690738 | |||||||
| chr11:110690870 | G | C | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.106-241C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110690870 | |||||||
| chr11:110690905 | A | G | 3 | a0001c0001t0001g0137 a0003c0004t0002g0142 a0012c0017t0002g0139 |
3 | HG00735.hp2 HG03688.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.106-276T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110690905 | |||||||
| chr11:110691189 | T | G | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-560A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691189 | |||||||
| chr11:110691256 | T | C | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.106-627A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691256 | |||||||
| chr11:110691333 | G | C | 6 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-704C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691333 | |||||||
| chr11:110691366 | TA | T | 3 | a0001c0001t0006g0196 a0001c0001t0006g0197 a0001c0001t0006g0198 |
3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.106-738delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691366 | |||||||
| chr11:110691388 | C | T | 1 | a0001c0001t0009g0004 | 2 | HG00639.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.106-759G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691388 | |||||||
| chr11:110691591 | T | A | 1 | a0001c0002t0005g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.106-962A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691591 | |||||||
| chr11:110691702 | C | T | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.106-1073G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691702 | |||||||
| chr11:110691855 | A | G | 36 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0200 others(33): Show |
36 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.106-1226T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691855 | |||||||
| chr11:110691968 | T | C | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.106-1339A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691968 | |||||||
| chr11:110691989 | G | A | 1 | a0001c0001t0004g0014 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.106-1360C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110691989 | |||||||
| chr11:110692100 | T | C | 1 | a0001c0001t0002g0045 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.106-1471A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110692100 | |||||||
| chr11:110692176 | T | C | 4 | a0001c0001t0001g0029 a0001c0001t0001g0106 a0001c0001t0002g0125 others(1): Show |
4 | HG01496.hp2 HG01516.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-1547A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110692176 | |||||||
| chr11:110692365 | G | C | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.106-1736C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110692365 | |||||||
| chr11:110692643 | C | T | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.106-2014G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110692643 | |||||||
| chr11:110692715 | A | C | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-2086T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110692715 | |||||||
| chr11:110692741 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.106-2112A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110692741 | |||||||
| chr11:110692880 | T | C | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-2251A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110692880 | |||||||
| chr11:110692976 | A | G | 1 | a0001c0001t0002g0031 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.106-2347T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110692976 | |||||||
| chr11:110693175 | G | A | 5 | a0001c0001t0002g0046 a0001c0001t0003g0047 a0001c0001t0003g0107 others(2): Show |
5 | HG01192.hp1 HG02273.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-2546C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110693175 | |||||||
| chr11:110693263 | T | C | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.106-2634A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110693263 | |||||||
| chr11:110693633 | C | G | 1 | a0011c0015t0004g0151 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.106-3004G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110693633 | |||||||
| chr11:110693637 | A | C | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.106-3008T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110693637 | |||||||
| chr11:110693691 | T | C | 6 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-3062A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110693691 | |||||||
| chr11:110693825 | T | C | 1 | a0001c0001t0013g0110 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.106-3196A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110693825 | |||||||
| chr11:110694021 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.106-3392G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110694021 | |||||||
| chr11:110694325 | G | C | 1 | a0001c0001t0006g0154 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.106-3696C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110694325 | |||||||
| chr11:110694368 | C | A | 1 | a0002c0006t0012g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.106-3739G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110694368 | |||||||
| chr11:110694458 | TA | T | 55 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(52): Show |
57 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.106-3830delT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110694458 | |||||||
| chr11:110694555 | C | T | 83 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(80): Show |
85 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.106-3926G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110694555 | |||||||
| chr11:110694606 | T | C | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.106-3977A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110694606 | |||||||
| chr11:110694713 | A | G | 11 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0003g0210 others(8): Show |
11 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.106-4084T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110694713 | |||||||
| chr11:110694982 | G | C | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.106-4353C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110694982 | |||||||
| chr11:110695181 | A | G | 6 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-4552T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695181 | |||||||
| chr11:110695402 | A | C | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.106-4773T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695402 | |||||||
| chr11:110695419 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.106-4790A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695419 | |||||||
| chr11:110695435 | A | G | 6 | a0001c0001t0002g0061 a0001c0001t0002g0063 a0001c0001t0002g0064 others(3): Show |
6 | HG01192.hp2 HG02055.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-4806T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695435 | |||||||
| chr11:110695497 | T | C | 1 | a0001c0001t0002g0112 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.106-4868A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695497 | |||||||
| chr11:110695529 | T | C | 35 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0200 others(32): Show |
35 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.106-4900A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695529 | |||||||
| chr11:110695539 | C | T | 1 | a0006c0011t0002g0126 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.106-4910G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695539 | |||||||
| chr11:110695550 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.106-4921A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695550 | |||||||
| chr11:110695711 | C | T | 1 | a0001c0002t0005g0113 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.106-5082G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695711 | |||||||
| chr11:110695903 | C | A | 55 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(52): Show |
57 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.106-5274G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695903 | |||||||
| chr11:110695978 | G | A | 55 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(52): Show |
57 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.106-5349C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110695978 | |||||||
| chr11:110696264 | T | C | 35 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0200 others(32): Show |
35 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.106-5635A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696264 | |||||||
| chr11:110696280 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.106-5651G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696280 | |||||||
| chr11:110696423 | T | G | 2 | a0001c0009t0002g0185 a0001c0009t0002g0193 |
2 | NA18978.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.106-5794A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696423 | |||||||
| chr11:110696471 | A | AT | 47 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(44): Show |
48 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.106-5843dupA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696471 | |||||||
| chr11:110696502 | G | C | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.106-5873C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696502 | |||||||
| chr11:110696569 | A | T | 4 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(1): Show |
4 | HG02109.hp1 HG02486.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.106-5940T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696569 | |||||||
| chr11:110696583 | T | TCATGTG | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.106-5960_106-5955d others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696583 | |||||||
| chr11:110696616 | C | T | 83 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(80): Show |
85 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.106-5987G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696616 | |||||||
| chr11:110696730 | C | T | 1 | a0001c0001t0003g0121 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.106-6101G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696730 | |||||||
| chr11:110696762 | T | C | 35 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0200 others(32): Show |
35 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.106-6133A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696762 | |||||||
| chr11:110696818 | G | T | 1 | a0002c0003t0007g0148 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.106-6189C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696818 | |||||||
| chr11:110696833 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0003g0128 |
2 | NA18983.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.106-6204G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696833 | |||||||
| chr11:110696844 | T | C | 8 | a0001c0001t0002g0010 a0001c0001t0004g0011 a0001c0001t0004g0012 others(5): Show |
8 | HG02145.hp2 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.106-6215A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696844 | |||||||
| chr11:110696872 | C | T | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.106-6243G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696872 | |||||||
| chr11:110696946 | A | G | 1 | a0001c0001t0016g0059 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.106-6317T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110696946 | |||||||
| chr11:110697062 | A | G | 1 | a0001c0001t0014g0008 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.106-6433T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110697062 | |||||||
| chr11:110697159 | A | G | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-6530T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110697159 | |||||||
| chr11:110697302 | A | G | 55 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(52): Show |
57 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.106-6673T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110697302 | |||||||
| chr11:110697531 | G | T | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-6902C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110697531 | |||||||
| chr11:110697677 | G | A | 1 | a0007c0018t0015g0009 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.106-7048C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110697677 | |||||||
| chr11:110698018 | T | C | 47 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(44): Show |
48 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.106-7389A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698018 | |||||||
| chr11:110698072 | A | G | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.106-7443T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698072 | |||||||
| chr11:110698127 | C | T | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.106-7498G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698127 | |||||||
| chr11:110698163 | A | G | 35 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0200 others(32): Show |
35 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.106-7534T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698163 | |||||||
| chr11:110698242 | A | G | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.106-7613T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698242 | |||||||
| chr11:110698314 | C | T | 47 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(44): Show |
48 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.106-7685G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698314 | |||||||
| chr11:110698389 | A | G | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.106-7760T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698389 | |||||||
| chr11:110698566 | A | G | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.106-7937T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698566 | |||||||
| chr11:110698627 | C | A | 1 | a0001c0001t0002g0055 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.106-7998G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698627 | |||||||
| chr11:110698701 | G | T | 1 | a0001c0001t0001g0029 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.106-8072C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698701 | |||||||
| chr11:110698908 | T | C | 35 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0200 others(32): Show |
35 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.106-8279A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110698908 | |||||||
| chr11:110699092 | C | T | 47 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(44): Show |
48 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.106-8463G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699092 | |||||||
| chr11:110699114 | A | G | 3 | a0001c0001t0006g0196 a0001c0001t0006g0197 a0001c0001t0006g0198 |
3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.106-8485T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699114 | |||||||
| chr11:110699170 | G | T | 47 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(44): Show |
48 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.106-8541C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699170 | |||||||
| chr11:110699305 | G | A | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.106-8676C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699305 | |||||||
| chr11:110699548 | TGTA | T | 2 | a0006c0011t0002g0030 a0006c0011t0002g0126 |
2 | NA19075.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.106-8922_106-8920d others(5): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699548 | |||||||
| chr11:110699602 | T | C | 2 | a0001c0001t0001g0049 a0001c0001t0002g0048 |
2 | HG00558.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.106-8973A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699602 | |||||||
| chr11:110699604 | T | C | 1 | a0013c0019t0004g0149 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.106-8975A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699604 | |||||||
| chr11:110699729 | T | C | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.106-9100A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699729 | |||||||
| chr11:110699765 | C | T | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.106-9136G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699765 | |||||||
| chr11:110699863 | T | C | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.106-9234A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699863 | |||||||
| chr11:110699875 | C | T | 47 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(44): Show |
48 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.106-9246G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110699875 | |||||||
| chr11:110700323 | T | C | 6 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
7 | HG00280.hp1 HG00639.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.106-9694A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700323 | |||||||
| chr11:110700405 | GACT | G | 6 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-9779_106-9777d others(5): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700405 | |||||||
| chr11:110700565 | C | A | 1 | a0001c0001t0002g0028 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.106-9936G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700565 | |||||||
| chr11:110700565 | CT | C | 20 | a0001c0001t0001g0137 a0001c0001t0001g0207 a0001c0001t0003g0209 others(17): Show |
21 | HG00099.hp2 HG00280.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.106-9937delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700565 | |||||||
| chr11:110700568 | T | C | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.106-9939A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700568 | |||||||
| chr11:110700678 | T | C | 83 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(80): Show |
85 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.106-10049A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700678 | |||||||
| chr11:110700680 | C | A | 6 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-10051G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700680 | |||||||
| chr11:110700738 | C | A | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.106-10109G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700738 | |||||||
| chr11:110700835 | C | A | 1 | a0012c0017t0002g0139 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.106-10206G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700835 | |||||||
| chr11:110700844 | G | C | 6 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-10215C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110700844 | |||||||
| chr11:110701098 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG01261.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.106-10469G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701098 | |||||||
| chr11:110701159 | C | T | 5 | a0001c0001t0002g0010 a0001c0001t0004g0011 a0001c0001t0004g0012 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.106-10530G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701159 | |||||||
| chr11:110701184 | G | A | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.106-10555C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701184 | |||||||
| chr11:110701198 | T | TCCCA | 6 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-10570_106-1056 others(8): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701198 | |||||||
| chr11:110701220 | T | C | 19 | a0001c0001t0001g0207 a0001c0001t0002g0200 a0001c0001t0002g0201 others(16): Show |
19 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.106-10591A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701220 | |||||||
| chr11:110701282 | C | G | 3 | a0001c0001t0006g0196 a0001c0001t0006g0197 a0001c0001t0006g0198 |
3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.106-10653G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701282 | |||||||
| chr11:110701333 | C | A | 1 | a0001c0001t0002g0050 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.106-10704G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701333 | |||||||
| chr11:110701346 | G | A | 6 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.106-10717C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701346 | |||||||
| chr11:110701507 | G | A | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.105+10620C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701507 | |||||||
| chr11:110701523 | T | G | 1 | a0001c0001t0003g0056 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.105+10604A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701523 | |||||||
| chr11:110701665 | T | G | 1 | a0001c0001t0006g0183 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.105+10462A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701665 | |||||||
| chr11:110701813 | T | C | 3 | a0001c0001t0004g0006 a0001c0001t0004g0141 a0001c0005t0005g0140 |
4 | HG01891.hp1 HG03098.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+10314A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701813 | |||||||
| chr11:110701904 | G | A | 11 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0003g0210 others(8): Show |
11 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.105+10223C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701904 | |||||||
| chr11:110701952 | G | T | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.105+10175C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110701952 | |||||||
| chr11:110702058 | C | T | 4 | a0001c0001t0002g0156 a0001c0001t0002g0157 a0001c0001t0002g0158 others(1): Show |
4 | HG00673.hp2 HG02040.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+10069G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702058 | |||||||
| chr11:110702063 | C | T | 2 | a0001c0001t0001g0029 a0011c0015t0004g0151 |
2 | HG01496.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.105+10064G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702063 | |||||||
| chr11:110702211 | G | A | 1 | a0002c0003t0007g0205 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.105+9916C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702211 | |||||||
| chr11:110702220 | G | T | 1 | a0003c0004t0017g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.105+9907C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702220 | |||||||
| chr11:110702278 | C | G | 1 | a0001c0001t0003g0056 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.105+9849G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702278 | |||||||
| chr11:110702320 | T | G | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.105+9807A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702320 | |||||||
| chr11:110702434 | G | T | 1 | a0001c0001t0014g0008 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.105+9693C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702434 | |||||||
| chr11:110702538 | C | A | 12 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0003g0210 others(9): Show |
12 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.105+9589G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702538 | |||||||
| chr11:110702718 | C | A | 28 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0003g0209 others(25): Show |
28 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.105+9409G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702718 | |||||||
| chr11:110702743 | G | C | 1 | a0001c0001t0001g0184 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.105+9384C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702743 | |||||||
| chr11:110702749 | T | C | 56 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(53): Show |
58 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.105+9378A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702749 | |||||||
| chr11:110702824 | T | C | 83 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(80): Show |
85 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.105+9303A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702824 | |||||||
| chr11:110702958 | C | T | 55 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(52): Show |
57 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.105+9169G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110702958 | |||||||
| chr11:110703025 | G | C | 1 | a0010c0020t0020g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.105+9102C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703025 | |||||||
| chr11:110703038 | C | T | 4 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(1): Show |
4 | HG00738.hp2 HG01099.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+9089G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703038 | |||||||
| chr11:110703060 | A | C | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.105+9067T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703060 | |||||||
| chr11:110703146 | T | C | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.105+8981A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703146 | |||||||
| chr11:110703201 | G | T | 2 | a0001c0001t0003g0001 a0001c0001t0003g0051 |
4 | HG01928.hp2 HG01981.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.105+8926C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703201 | |||||||
| chr11:110703326 | A | G | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.105+8801T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703326 | |||||||
| chr11:110703407 | A | G | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+8720T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703407 | |||||||
| chr11:110703410 | T | C | 44 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(41): Show |
45 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.105+8717A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703410 | |||||||
| chr11:110703637 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.105+8490C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703637 | |||||||
| chr11:110703678 | C | A | 3 | a0001c0001t0004g0144 a0003c0004t0017g0143 a0010c0020t0020g0147 |
3 | HG03225.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.105+8449G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703678 | |||||||
| chr11:110703710 | A | G | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+8417T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703710 | |||||||
| chr11:110703717 | T | C | 1 | a0001c0001t0008g0021 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.105+8410A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703717 | |||||||
| chr11:110703823 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.105+8304G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703823 | |||||||
| chr11:110703889 | A | G | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.105+8238T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703889 | |||||||
| chr11:110703967 | G | A | 47 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(44): Show |
48 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.105+8160C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110703967 | |||||||
| chr11:110704110 | C | A | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.105+8017G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704110 | |||||||
| chr11:110704256 | T | C | 1 | a0001c0002t0005g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.105+7871A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704256 | |||||||
| chr11:110704288 | C | T | 2 | a0001c0001t0004g0144 a0003c0004t0017g0143 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.105+7839G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704288 | |||||||
| chr11:110704389 | A | G | 12 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0003g0210 others(9): Show |
12 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.105+7738T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704389 | |||||||
| chr11:110704556 | T | C | 35 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0002g0200 others(32): Show |
35 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(32): Show |
intron_variant | MODIFIER | c.105+7571A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704556 | |||||||
| chr11:110704576 | GC | G | 29 | a0001c0001t0001g0039 a0001c0001t0001g0049 a0001c0001t0002g0026 others(26): Show |
29 | HG00558.hp2 HG01358.hp2 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.105+7550delG | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704576 | |||||||
| chr11:110704710 | T | G | 1 | a0001c0001t0003g0005 | 2 | NA18942.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.105+7417A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704710 | |||||||
| chr11:110704745 | G | A | 19 | a0001c0001t0001g0207 a0001c0001t0002g0200 a0001c0001t0002g0201 others(16): Show |
19 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.105+7382C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704745 | |||||||
| chr11:110704768 | A | C | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.105+7359T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704768 | |||||||
| chr11:110704866 | G | T | 1 | a0002c0006t0012g0138 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.105+7261C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704866 | |||||||
| chr11:110704990 | A | G | 2 | a0001c0001t0001g0029 a0001c0001t0002g0125 |
2 | HG01496.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.105+7137T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110704990 | |||||||
| chr11:110705009 | C | A | 7 | a0001c0001t0002g0200 a0001c0001t0002g0201 a0001c0001t0002g0202 others(4): Show |
7 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.105+7118G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705009 | |||||||
| chr11:110705191 | G | A | 48 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(45): Show |
49 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.105+6936C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705191 | |||||||
| chr11:110705207 | C | T | 55 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(52): Show |
57 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.105+6920G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705207 | |||||||
| chr11:110705302 | A | G | 1 | a0002c0003t0007g0148 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.105+6825T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705302 | |||||||
| chr11:110705465 | A | G | 44 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(41): Show |
45 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.105+6662T>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705465 | |||||||
| chr11:110705549 | C | T | 48 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(45): Show |
49 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.105+6578G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705549 | |||||||
| chr11:110705632 | G | A | 1 | a0001c0001t0009g0118 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.105+6495C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705632 | |||||||
| chr11:110705727 | C | A | 1 | a0001c0001t0002g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.105+6400G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705727 | |||||||
| chr11:110705807 | A | C | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+6320T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705807 | |||||||
| chr11:110705850 | C | T | 1 | a0001c0001t0002g0028 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.105+6277G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705850 | |||||||
| chr11:110705871 | G | A | 6 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.105+6256C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705871 | |||||||
| chr11:110705912 | G | A | 83 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(80): Show |
85 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.105+6215C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110705912 | |||||||
| chr11:110706105 | C | T | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.105+6022G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110706105 | |||||||
| chr11:110706323 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.105+5804G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110706323 | |||||||
| chr11:110706362 | T | A | 1 | a0001c0001t0001g0153 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.105+5765A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110706362 | |||||||
| chr11:110706581 | T | C | 1 | a0001c0001t0002g0120 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.105+5546A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110706581 | |||||||
| chr11:110706593 | ACCTACTC others(48): Show |
A | 1 | a0001c0002t0005g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.105+5479_105+5533d others(57): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110706593 | |||||||
| chr11:110707571 | T | A | 1 | a0003c0004t0002g0142 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.105+4556A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110707571 | |||||||
| chr11:110707575 | C | T | 1 | a0001c0001t0002g0026 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.105+4552G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110707575 | |||||||
| chr11:110707625 | T | C | 22 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0003g0209 others(19): Show |
22 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.105+4502A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110707625 | |||||||
| chr11:110707831 | A | C | 6 | a0001c0001t0006g0154 a0001c0001t0006g0196 a0001c0001t0006g0197 others(3): Show |
6 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.105+4296T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110707831 | |||||||
| chr11:110707863 | GT | G | 75 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(72): Show |
76 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.105+4263delA | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110707863 | |||||||
| chr11:110707924 | G | A | 2 | a0001c0009t0002g0185 a0001c0009t0002g0193 |
2 | NA18978.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.105+4203C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110707924 | |||||||
| chr11:110708002 | C | T | 2 | a0001c0001t0002g0024 a0001c0001t0002g0025 |
2 | HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.105+4125G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708002 | |||||||
| chr11:110708201 | A | C | 47 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(44): Show |
48 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.105+3926T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708201 | |||||||
| chr11:110708246 | T | C | 8 | a0001c0001t0002g0010 a0001c0001t0004g0011 a0001c0001t0004g0012 others(5): Show |
8 | HG02145.hp2 HG02647.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+3881A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708246 | |||||||
| chr11:110708452 | T | TTTTA | 76 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(73): Show |
77 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.105+3674_105+3675i others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708452 | |||||||
| chr11:110708567 | G | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0216 others(1): Show |
4 | HG00099.hp1 HG00741.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.105+3560C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708567 | |||||||
| chr11:110708652 | C | A | 1 | a0001c0002t0005g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.105+3475G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708652 | |||||||
| chr11:110708653 | A | C | 1 | a0001c0002t0005g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.105+3474T>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708653 | |||||||
| chr11:110708654 | T | A | 1 | a0001c0002t0005g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.105+3473A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708654 | |||||||
| chr11:110708667 | T | A | 1 | a0001c0002t0005g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.105+3460A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708667 | |||||||
| chr11:110708669 | T | TTGAAGAA others(47): Show |
1 | a0001c0002t0005g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.105+3457_105+3458i others(56): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708669 | |||||||
| chr11:110708674 | G | A | 55 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(52): Show |
57 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.105+3453C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708674 | |||||||
| chr11:110708675 | T | G | 1 | a0001c0002t0005g0206 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.105+3452A>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708675 | |||||||
| chr11:110708714 | T | C | 12 | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0001t0003g0210 others(9): Show |
12 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.105+3413A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708714 | |||||||
| chr11:110708726 | G | A | 1 | a0001c0001t0003g0124 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.105+3401C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110708726 | |||||||
| chr11:110709280 | G | A | 1 | a0001c0012t0002g0186 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.105+2847C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110709280 | |||||||
| chr11:110709363 | G | C | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.105+2764C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110709363 | |||||||
| chr11:110709415 | T | A | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+2712A>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110709415 | |||||||
| chr11:110709560 | G | C | 2 | a0005c0007t0010g0145 a0005c0007t0010g0146 |
2 | HG02622.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.105+2567C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110709560 | |||||||
| chr11:110709874 | A | T | 28 | a0001c0001t0001g0207 a0001c0001t0002g0010 a0001c0001t0003g0209 others(25): Show |
28 | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.105+2253T>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110709874 | |||||||
| chr11:110709900 | C | A | 1 | a0001c0001t0013g0187 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.105+2227G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110709900 | |||||||
| chr11:110709956 | C | T | 1 | a0001c0001t0006g0196 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.105+2171G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110709956 | |||||||
| chr11:110709957 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.105+2170C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110709957 | |||||||
| chr11:110710141 | G | A | 90 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(87): Show |
92 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.105+1986C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110710141 | |||||||
| chr11:110710435 | T | TA | 65 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(62): Show |
67 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.105+1691dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110710435 | |||||||
| chr11:110710878 | C | T | 19 | a0001c0001t0001g0207 a0001c0001t0002g0200 a0001c0001t0002g0201 others(16): Show |
19 | HG00099.hp2 HG00280.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.105+1249G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110710878 | |||||||
| chr11:110711005 | C | CA | 30 | a0001c0001t0001g0022 a0001c0001t0001g0127 a0001c0001t0001g0130 others(27): Show |
31 | HG00099.hp2 HG00280.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.105+1121dupT | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711005 | |||||||
| chr11:110711005 | C | CAA | 17 | a0001c0001t0002g0010 a0001c0001t0002g0200 a0001c0001t0002g0201 others(14): Show |
17 | HG01074.hp1 HG01891.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.105+1120_105+1121d others(4): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711005 | |||||||
| chr11:110711005 | C | CAAA | 9 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0153 others(6): Show |
9 | HG02109.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.105+1119_105+1121d others(5): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711005 | |||||||
| chr11:110711005 | C | CAAAA | 40 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 others(37): Show |
41 | HG00639.hp2 HG00673.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.105+1118_105+1121d others(6): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711005 | |||||||
| chr11:110711005 | C | CAAAAA | 5 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
5 | HG00621.hp1 HG03098.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.105+1117_105+1121d others(7): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711005 | |||||||
| chr11:110711033 | G | T | 7 | a0001c0001t0001g0137 a0001c0001t0004g0006 a0001c0001t0004g0141 others(4): Show |
8 | HG00735.hp2 HG01891.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.105+1094C>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711033 | |||||||
| chr11:110711267 | C | T | 1 | a0001c0001t0003g0023 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.105+860G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711267 | |||||||
| chr11:110711447 | G | A | 1 | a0001c0005t0005g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.105+680C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711447 | |||||||
| chr11:110711587 | T | C | 89 | a0001c0001t0001g0007 a0001c0001t0001g0137 a0001c0001t0001g0150 others(86): Show |
91 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.105+540A>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711587 | |||||||
| chr11:110711625 | C | G | 1 | a0001c0001t0001g0022 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.105+502G>C | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711625 | |||||||
| chr11:110711645 | C | T | 6 | a0001c0001t0001g0019 a0001c0001t0008g0016 a0001c0001t0008g0017 others(3): Show |
6 | HG02155.hp1 NA18972.hp2 NA18997.hp1 others(3): Show |
intron_variant | MODIFIER | c.105+482G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711645 | |||||||
| chr11:110711648 | C | T | 1 | a0001c0001t0003g0015 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.105+479G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711648 | |||||||
| chr11:110711807 | C | T | 5 | a0001c0001t0002g0010 a0001c0001t0004g0011 a0001c0001t0004g0012 others(2): Show |
5 | HG02145.hp2 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.105+320G>A | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711807 | |||||||
| chr11:110711904 | G | A | 1 | a0001c0001t0003g0195 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.105+223C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711904 | |||||||
| chr11:110711937 | G | C | 3 | a0001c0001t0006g0196 a0001c0001t0006g0197 a0001c0001t0006g0198 |
3 | HG02109.hp1 HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.105+190C>G | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110711937 | |||||||
| chr11:110712091 | C | A | 19 | a0001c0001t0001g0207 a0001c0001t0001g0216 a0001c0001t0002g0200 others(16): Show |
19 | HG00099.hp2 HG00741.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.105+36G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110712091 | |||||||
| chr11:110712092 | G | A | 20 | a0001c0001t0001g0207 a0001c0001t0001g0216 a0001c0001t0002g0200 others(17): Show |
20 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.105+35C>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110712092 | |||||||
| chr11:110712111 | C | A | 13 | a0001c0001t0001g0207 a0001c0001t0001g0216 a0001c0001t0003g0209 others(10): Show |
13 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.105+16G>T | ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 1/14 | chr11 | 110712111 |