Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 93663 |
|---|---|
| ensemblid | ENSG00000146376.11 |
| hgncid | 21035 |
| symbol | ARHGAP18 |
| name | Rho GTPase activating protein 18 |
| refseq_nuc | NM_033515.3 |
| refseq_prot | NP_277050.2 |
| ensembl_nuc | ENST00000368149.3 |
| ensembl_prot | ENSP00000357131.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 129576132 |
| end | 129710177 |
| strand | - |
| ver | v1.2 |
| region | chr6:129576132-129710177 |
| region5000 | chr6:129571132-129715177 |
| regionname0 | ARHGAP18_chr6_129576132_129710177 |
| regionname5000 | ARHGAP18_chr6_129571132_129715177 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 663 | 179 | 50 | 40 | 65 | 9 | 15 | 40 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0002 | 1/1 | 663 | 51 | 8 | 10 | 28 | 1 | 2 | 17 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0003 | 0/0 | 663 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0004 | 0/0 | 663 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0005 | 0/0 | 663 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0006 | 0/0 | 663 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0007 | 0/0 | 663 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0008 | 0/0 | 663 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0009 | 0/0 | 663 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1992 | 174 | 48 | 39 | 65 | 8 | 14 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| c0002 | 1/1 | 1992 | 50 | 8 | 10 | 27 | 1 | 2 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| c0003 | 0/0 | 1992 | 3 | 1 | 0 | 0 | 1 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| c0004 | 0/0 | 1992 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| c0005 | 0/0 | 1992 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| c0006 | 0/0 | 1992 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| c0007 | 0/0 | 1992 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| c0008 | 0/0 | 1992 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| c0009 | 0/0 | 1992 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| c0010 | 0/0 | 1992 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| c0011 | 0/0 | 1992 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| c0012 | 0/0 | 1992 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| c0013 | 0/0 | 1992 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2423 | 143 | 21 | 40 | 63 | 8 | 9 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| t0002 | 0/0 | 2422 | 47 | 13 | 8 | 16 | 2 | 8 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| t0003 | 0/0 | 2423 | 21 | 13 | 1 | 7 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| t0004 | 0/0 | 2420 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| t0005 | 0/0 | 2425 | 4 | 1 | 0 | 3 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| t0006 | 0/0 | 2420 | 3 | 0 | 0 | 0 | 0 | 3 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| t0007 | 0/0 | 2423 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| t0008 | 0/0 | 2423 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| t0009 | 0/0 | 2425 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| t0010 | 0/0 | 2420 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| t0011 | 0/0 | 2420 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| t0012 | 0/0 | 2422 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| t0013 | 0/0 | 2422 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| t0014 | 0/0 | 2423 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| t0015 | 0/0 | 2423 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| t0016 | 0/0 | 2423 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| t0017 | 0/0 | 2423 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| t0018 | 0/0 | 2423 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| t0019 | 0/0 | 2423 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0005 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1992 | 174 | 48 | 39 | 65 | 8 | 14 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0003 | 0/0 | 1992 | 3 | 1 | 0 | 0 | 1 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0009 | 0/0 | 1992 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0011 | 0/0 | 1992 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0002c0002 | 1/1 | 1992 | 50 | 8 | 10 | 27 | 1 | 2 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0002c0006 | 0/0 | 1992 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0003c0004 | 0/0 | 1992 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0004c0013 | 0/0 | 1992 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0005c0012 | 0/0 | 1992 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0006c0010 | 0/0 | 1992 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0007c0008 | 0/0 | 1992 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0008c0005 | 0/0 | 1992 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0009c0007 | 0/0 | 1992 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4414 | 105 | 15 | 33 | 44 | 7 | 6 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0001t0002 | 0/0 | 4413 | 35 | 11 | 6 | 11 | 1 | 6 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0001t0003 | 0/0 | 4414 | 14 | 10 | 0 | 4 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0001t0004 | 0/0 | 4411 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0001t0005 | 0/0 | 4416 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0001t0006 | 0/0 | 4411 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0001t0007 | 0/0 | 4414 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0001t0008 | 0/0 | 4414 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0001t0009 | 0/0 | 4416 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0001t0010 | 0/0 | 4411 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0001t0011 | 0/0 | 4411 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0001t0013 | 0/0 | 4413 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0001t0015 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0001t0016 | 0/0 | 4414 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0001t0017 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0001t0019 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0003t0002 | 0/0 | 4413 | 3 | 1 | 0 | 0 | 1 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0009t0001 | 0/0 | 4414 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0001c0011t0001 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0002c0002t0001 | 1/1 | 4414 | 32 | 4 | 6 | 18 | 1 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0002c0002t0002 | 0/0 | 4413 | 8 | 1 | 2 | 5 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0002c0002t0003 | 0/0 | 4414 | 6 | 2 | 1 | 3 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0002c0002t0005 | 0/0 | 4416 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0002c0002t0006 | 0/0 | 4411 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0002c0002t0014 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0002c0002t0018 | 0/0 | 4414 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0002c0006t0012 | 0/0 | 4413 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0003c0004t0001 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0003c0004t0005 | 0/0 | 4416 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0004c0013t0001 | 0/0 | 4414 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0005c0012t0002 | 0/0 | 4413 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0006c0010t0001 | 0/0 | 4414 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0007c0008t0004 | 0/0 | 4411 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0008c0005t0003 | 0/0 | 4414 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| a0009c0007t0001 | 0/0 | 4414 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | copy fasta | chr6 | 129571132 | 129715177 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0006g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0006g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0008g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0008g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0009g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0009g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0010g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0011g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0013g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0015g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0016g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0017g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0001t0019g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0003t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0003t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0009t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0001c0011t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0005 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0006g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0014g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0002t0018g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0002c0006t0012g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0003c0004t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0003c0004t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0004c0013t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0005c0012t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0006c0010t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0007c0008t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0008c0005t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| a0009c0007t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0002 | g0190 | EUR | GBR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | GBR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | GBR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | GBR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00558 | hp1 | a0002 | c0002 | t0003 | g0023 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00597 | hp2 | a0001 | c0001 | t0005 | g0207 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | CHS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00733 | hp2 | a0002 | c0002 | t0018 | g0009 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01099 | hp2 | a0001 | c0009 | t0001 | g0122 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01192 | hp2 | a0002 | c0002 | t0003 | g0027 | AMR | PUR | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | CLM | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | CLM | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | IBS | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0050 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02027 | hp2 | a0001 | c0001 | t0016 | g0149 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02129 | hp1 | a0002 | c0002 | t0003 | g0022 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | CDX | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | CDX | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0020 | AMR | PEL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02451 | hp2 | a0002 | c0002 | t0003 | g0043 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02615 | hp1 | a0001 | c0001 | t0011 | g0141 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02615 | hp2 | a0007 | c0008 | t0004 | g0055 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0123 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0052 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0225 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02717 | hp1 | a0001 | c0001 | t0015 | g0110 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0044 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0077 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0118 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02965 | hp1 | a0008 | c0005 | t0003 | g0002 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0223 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0133 | AFR | MSL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03098 | hp2 | a0003 | c0004 | t0001 | g0151 | AFR | MSL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0224 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03130 | hp2 | a0001 | c0001 | t0017 | g0174 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0137 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0226 | AFR | MSL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03209 | hp2 | a0001 | c0011 | t0001 | g0056 | AFR | MSL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0134 | AFR | MSL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0028 | AFR | MSL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03491 | hp1 | a0002 | c0002 | t0006 | g0032 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0128 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03540 | hp2 | a0002 | c0002 | t0014 | g0045 | AFR | GWD | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03669 | hp2 | a0001 | c0003 | t0002 | g0211 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03704 | hp2 | a0006 | c0010 | t0001 | g0197 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0167 | SAS | BEB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0060 | SAS | BEB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG04115 | hp1 | a0005 | c0012 | t0002 | g0095 | SAS | STU | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG04115 | hp2 | a0004 | c0013 | t0001 | g0208 | SAS | STU | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0031 | SAS | STU | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG04228 | hp2 | a0001 | c0001 | t0006 | g0198 | SAS | STU | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18522 | hp1 | a0002 | c0002 | t0003 | g0029 | AFR | YRI | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | YRI | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18612 | hp1 | a0001 | c0001 | t0009 | g0071 | EAS | CHB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | CHB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18954 | hp1 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18983 | hp1 | a0001 | c0001 | t0013 | g0119 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18987 | hp1 | a0002 | c0002 | t0003 | g0037 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19004 | hp1 | a0002 | c0002 | t0005 | g0024 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19011 | hp1 | a0001 | c0001 | t0005 | g0212 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19043 | hp1 | a0001 | c0001 | t0019 | g0233 | AFR | LWK | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | LWK | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19056 | hp2 | a0002 | c0006 | t0012 | g0034 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19070 | hp2 | a0009 | c0007 | t0001 | g0030 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19090 | hp2 | a0001 | c0001 | t0009 | g0069 | EAS | JPT | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | YRI | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0082 | EUR | TSI | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0053 | EUR | TSI | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | TSI | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | ACB | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0228 | AFR | USA | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| HG06807 | hp2 | a0001 | c0003 | t0002 | g0175 | AFR | USA | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA20300 | hp1 | a0003 | c0004 | t0005 | g0088 | AFR | USA | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | USA | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0005 | REF | REF | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0001 | g0003 | REF | REF | ARHGAP18_chr6_129571132_129715177 | ARHGAP18 | chr6 | 129571132 | 129715177 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:129584076
|
G | A | 1 | a0005 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.1750C>T | p.Pro584Ser | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/15 | 1791/4414 | 1750/1992 | 584/663 | chr6 | 129584076 | ||
| chr6:129599221
|
T | C | 1 | a0009 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.1708A>G | p.Asn570Asp | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/15 | 1749/4414 | 1708/1992 | 570/663 | chr6 | 129599221 | ||
| chr6:129608031
|
C | T | 1 | a0006 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.1144G>A | p.Ala382Thr | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/15 | 1185/4414 | 1144/1992 | 382/663 | chr6 | 129608031 | ||
| chr6:129629396
|
T | C | 1 | a0003 | 2 | HG03098.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.743A>G | p.Lys248Arg | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/15 | 784/4414 | 743/1992 | 248/663 | chr6 | 129629396 | ||
| chr6:129634101
|
G | A | 1 | a0004 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.557C>T | p.Pro186Leu | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/15 | 598/4414 | 557/1992 | 186/663 | chr6 | 129634101 | ||
| chr6:129710043
|
C | T | 1 | a0007 | 1 | HG02615.hp2 | missense_variant | MODERATE | c.94G>A | p.Gly32Arg | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/15 | 135/4414 | 94/1992 | 32/663 | chr6 | 129710043 | ||
| chr6:129710066
|
A | G | 1 | a0008 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.71T>C | p.Val24Ala | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/15 | 112/4414 | 71/1992 | 24/663 | chr6 | 129710066 | ||
| chr6:129710070
|
T | C | 6 | a0001a0003a0004others(3): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
missense_variant | MODERATE | c.67A>G | p.Thr23Ala | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/15 | 108/4414 | 67/1992 | 23/663 | chr6 | 129710070 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:129584104
|
A | G | 2 | a0001c0003a0002c0006 | 4 | HG00099.hp1 HG03669.hp2 HG06807.hp2 others(1): Show |
synonymous_variant | LOW | c.1722T>C | p.Val574Val | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/15 | 1763/4414 | 1722/1992 | 574/663 | chr6 | 129584104 | ||
| chr6:129600648
|
C | G | 1 | a0001c0011 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.1566G>C | p.Leu522Leu | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/15 | 1607/4414 | 1566/1992 | 522/663 | chr6 | 129600648 | ||
| chr6:129638484
|
C | T | 1 | a0001c0009 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.462G>A | p.Thr154Thr | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/15 | 503/4414 | 462/1992 | 154/663 | chr6 | 129638484 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:129576195
|
A | T | 1 | a0001c0001t0013 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2318T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 2318 | chr6 | 129576195 | |||||
| chr6:129576206
|
C | G | 4 | a0001c0001t0003a0001c0001t0008a0002c0002t0003others(1): Show | 23 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2307G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 2307 | chr6 | 129576206 | |||||
| chr6:129576390
|
G | T | 1 | a0002c0006t0012 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2123C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 2123 | chr6 | 129576390 | |||||
| chr6:129576411
|
C | T | 1 | a0001c0001t0016 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2102G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 2102 | chr6 | 129576411 | |||||
| chr6:129576554
|
G | C | 1 | a0001c0001t0011 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1959C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1959 | chr6 | 129576554 | |||||
| chr6:129576665
|
G | A | 2 | a0001c0001t0010a0001c0001t0011 | 2 | HG02615.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1848C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1848 | chr6 | 129576665 | |||||
| chr6:129576700
|
C | T | 1 | a0001c0001t0015 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1813G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1813 | chr6 | 129576700 | |||||
| chr6:129576725
|
T | C | 1 | a0001c0001t0017 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1788A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1788 | chr6 | 129576725 | |||||
| chr6:129576783
|
T | C | 1 | a0002c0002t0018 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1730A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1730 | chr6 | 129576783 | |||||
| chr6:129576922
|
A | G | 1 | a0002c0002t0014 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1591T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1591 | chr6 | 129576922 | |||||
| chr6:129577023
|
T | G | 1 | a0001c0001t0008 | 2 | HG02922.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1490A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1490 | chr6 | 129577023 | |||||
| chr6:129577033
|
TA | T | 6 | a0001c0001t0002a0001c0001t0013a0001c0003t0002others(3): Show | 49 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1479delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1479 | chr6 | 129577033 | |||||
| chr6:129577037
|
A | G | 8 | a0001c0001t0004a0001c0001t0006a0001c0001t0007others(5): Show | 12 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1476T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1476 | chr6 | 129577037 | |||||
| chr6:129577169
|
C | T | 6 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(3): Show | 9 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1344G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1344 | chr6 | 129577169 | |||||
| chr6:129577195
|
G | T | 6 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(3): Show | 9 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1318C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1318 | chr6 | 129577195 | |||||
| chr6:129577508
|
C | T | 2 | a0001c0001t0010a0001c0001t0011 | 2 | HG02615.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1005G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 1005 | chr6 | 129577508 | |||||
| chr6:129577586
|
T | TAA | 4 | a0001c0001t0005a0001c0001t0009a0002c0002t0005others(1): Show | 6 | HG00597.hp2 NA18612.hp1 NA19004.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*925_*926dupTT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 926 | chr6 | 129577586 | |||||
| chr6:129577621
|
C | A | 1 | a0001c0001t0019 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*892G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 892 | chr6 | 129577621 | |||||
| chr6:129577869
|
G | A | 2 | a0001c0001t0004a0007c0008t0004 | 4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*644C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 644 | chr6 | 129577869 | |||||
| chr6:129577982
|
A | G | 1 | a0001c0001t0009 | 2 | NA18612.hp1 NA19090.hp2 |
3_prime_UTR_variant | MODIFIER | c.*531T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 531 | chr6 | 129577982 | |||||
| chr6:129578141
|
G | A | 4 | a0001c0001t0005a0001c0001t0009a0002c0002t0005others(1): Show | 6 | HG00597.hp2 NA18612.hp1 NA19004.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*372C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 372 | chr6 | 129578141 | |||||
| chr6:129578291
|
C | T | 2 | a0001c0001t0006a0002c0002t0006 | 3 | HG03491.hp1 HG03834.hp2 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*222G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 222 | chr6 | 129578291 | |||||
| chr6:129578314
|
CTAA | C | 6 | a0001c0001t0004a0001c0001t0006a0001c0001t0010others(3): Show | 9 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*196_*198delTTA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 15/15 | 196 | chr6 | 129578314 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:129578990
|
A | T | 1 | a0001c0001t0002g0117 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1901-386T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 14/14 | chr6 | 129578990 | ||||||
| chr6:129579003
|
C | A | 11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0153others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1901-399G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 14/14 | chr6 | 129579003 | ||||||
| chr6:129579229
|
G | C | 4 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1901-625C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 14/14 | chr6 | 129579229 | ||||||
| chr6:129579275
|
T | C | 4 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1901-671A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 14/14 | chr6 | 129579275 | ||||||
| chr6:129579326
|
C | G | 19 | a0001c0001t0003g0075a0001c0001t0003g0128a0001c0001t0003g0133others(16): Show | 19 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.1901-722G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 14/14 | chr6 | 129579326 | ||||||
| chr6:129579464
|
T | A | 1 | a0001c0001t0001g0001 | 2 | HG00738.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1900+606A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 14/14 | chr6 | 129579464 | ||||||
| chr6:129579505
|
A | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0126a0002c0002t0001g0025 | 3 | HG02257.hp1 HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1900+565T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 14/14 | chr6 | 129579505 | ||||||
| chr6:129579822
|
A | C | 3 | a0001c0001t0001g0199a0002c0002t0001g0004a0002c0002t0001g0005 | 3 | HG00642.hp2 HG01074.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1900+248T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 14/14 | chr6 | 129579822 | ||||||
| chr6:129580016
|
C | G | 1 | a0001c0001t0001g0218 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1900+54G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 14/14 | chr6 | 129580016 | ||||||
| chr6:129580237
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1839-106A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129580237 | ||||||
| chr6:129580261
|
G | A | 1 | a0002c0002t0001g0026 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1839-130C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129580261 | ||||||
| chr6:129580293
|
A | G | 2 | a0001c0001t0002g0229a0001c0001t0002g0230 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1839-162T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129580293 | ||||||
| chr6:129580322
|
TTAAAA | T | 4 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1839-196_1839-192d others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129580322 | ||||||
| chr6:129580335
|
A | G | 3 | a0001c0001t0001g0079a0001c0001t0001g0136a0003c0004t0001g0151 | 3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1839-204T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129580335 | ||||||
| chr6:129580687
|
A | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0136a0003c0004t0001g0151 | 3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1839-556T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129580687 | ||||||
| chr6:129580998
|
C | A | 4 | a0001c0001t0001g0084a0001c0001t0001g0146a0001c0001t0001g0148others(1): Show | 4 | HG00423.hp2 HG02523.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.1839-867G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129580998 | ||||||
| chr6:129581187
|
T | G | 2 | a0002c0002t0001g0021a0002c0002t0001g0051 | 2 | NA18977.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1839-1056A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581187 | ||||||
| chr6:129581355
|
C | G | 1 | a0001c0001t0001g0114 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1839-1224G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581355 | ||||||
| chr6:129581369
|
C | T | 3 | a0001c0001t0001g0150a0001c0001t0001g0154a0001c0001t0001g0196 | 3 | HG00558.hp2 NA18987.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1839-1238G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581369 | ||||||
| chr6:129581376
|
G | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG00140.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.1839-1245C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581376 | ||||||
| chr6:129581448
|
AACT | A | 9 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(6): Show | 9 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1839-1320_1839-131 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581448 | ||||||
| chr6:129581494
|
T | G | 4 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1839-1363A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581494 | ||||||
| chr6:129581608
|
T | A | 47 | a0001c0001t0002g0057a0001c0001t0002g0066a0001c0001t0002g0068others(44): Show | 47 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.1839-1477A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581608 | ||||||
| chr6:129581660
|
C | T | 1 | a0002c0002t0002g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1839-1529G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581660 | ||||||
| chr6:129581879
|
C | T | 3 | a0001c0001t0001g0094a0001c0001t0001g0131a0001c0001t0001g0194 | 3 | HG02896.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1839-1748G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581879 | ||||||
| chr6:129581907
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1839-1776G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581907 | ||||||
| chr6:129581965
|
A | G | 3 | a0001c0001t0006g0060a0001c0001t0006g0198a0002c0002t0006g0032 | 3 | HG03491.hp1 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1839-1834T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129581965 | ||||||
| chr6:129582131
|
G | GAAGGAAT others(8): Show |
9 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(6): Show | 9 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1838+1842_1838+185 others(19): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129582131 | ||||||
| chr6:129582155
|
T | A | 236 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(233): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1838+1833A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129582155 | ||||||
| chr6:129582232
|
C | T | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1838+1756G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129582232 | ||||||
| chr6:129582358
|
T | C | 5 | a0001c0001t0006g0060a0001c0001t0006g0198a0001c0001t0010g0137others(2): Show | 5 | HG02615.hp1 HG03195.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1838+1630A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129582358 | ||||||
| chr6:129582373
|
A | G | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1838+1615T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129582373 | ||||||
| chr6:129582533
|
T | C | 1 | a0001c0001t0003g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1838+1455A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129582533 | ||||||
| chr6:129582626
|
G | C | 9 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(6): Show | 9 | HG02615.hp1 HG02615.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1838+1362C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129582626 | ||||||
| chr6:129582633
|
C | G | 4 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1838+1355G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129582633 | ||||||
| chr6:129582840
|
C | T | 1 | a0001c0001t0003g0219 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1838+1148G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129582840 | ||||||
| chr6:129583107
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1838+881C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583107 | ||||||
| chr6:129583159
|
G | A | 1 | a0001c0001t0003g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1838+829C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583159 | ||||||
| chr6:129583170
|
C | G | 10 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0153others(7): Show | 10 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.1838+818G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583170 | ||||||
| chr6:129583507
|
C | T | 5 | a0001c0001t0006g0060a0001c0001t0006g0198a0001c0001t0010g0137others(2): Show | 5 | HG02615.hp1 HG03195.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1838+481G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583507 | ||||||
| chr6:129583553
|
C | A | 17 | a0001c0001t0001g0074a0001c0001t0001g0086a0001c0001t0001g0105others(14): Show | 17 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.1838+435G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583553 | ||||||
| chr6:129583890
|
CA | C | 12 | a0001c0001t0001g0193a0001c0001t0002g0097a0001c0001t0002g0217others(9): Show | 12 | HG00597.hp2 HG02258.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.1838+97delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583890 | ||||||
| chr6:129583913
|
A | C | 1 | a0001c0001t0002g0184 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1838+75T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583913 | ||||||
| chr6:129583922
|
C | T | 3 | a0001c0001t0006g0060a0001c0001t0006g0198a0002c0002t0006g0032 | 3 | HG03491.hp1 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1838+66G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583922 | ||||||
| chr6:129583923
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0136a0003c0004t0001g0151 | 3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1838+65C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583923 | ||||||
| chr6:129583975
|
A | C | 7 | a0001c0001t0001g0161a0001c0001t0001g0186a0001c0001t0001g0201others(4): Show | 7 | HG00544.hp2 HG01358.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.1838+13T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 13/14 | chr6 | 129583975 | ||||||
| chr6:129584445
|
G | C | 1 | a0001c0001t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1714-333C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129584445 | ||||||
| chr6:129584503
|
T | A | 1 | a0001c0001t0001g0099 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1714-391A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129584503 | ||||||
| chr6:129584667
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1714-555T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129584667 | ||||||
| chr6:129584749
|
G | T | 4 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714-637C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129584749 | ||||||
| chr6:129584858
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0136a0003c0004t0001g0151 | 3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1714-746C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129584858 | ||||||
| chr6:129584877
|
A | T | 1 | a0001c0001t0001g0086 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1714-765T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129584877 | ||||||
| chr6:129584932
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1714-820A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129584932 | ||||||
| chr6:129585020
|
C | CT | 37 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0083others(34): Show | 37 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.1714-909dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585020 | ||||||
| chr6:129585020
|
CT | C | 66 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(63): Show | 66 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.1714-909delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585020 | ||||||
| chr6:129585020
|
CTT | C | 68 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0080others(65): Show | 68 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1714-910_1714-909d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585020 | ||||||
| chr6:129585027
|
T | A | 4 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714-915A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585027 | ||||||
| chr6:129585064
|
T | A | 3 | a0001c0001t0006g0060a0001c0001t0006g0198a0002c0002t0006g0032 | 3 | HG03491.hp1 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1714-952A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585064 | ||||||
| chr6:129585160
|
GC | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(233): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.1714-1049delG | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585160 | ||||||
| chr6:129585196
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1714-1084C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585196 | ||||||
| chr6:129585277
|
C | T | 4 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714-1165G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585277 | ||||||
| chr6:129585301
|
AAAAAT | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0136a0003c0004t0001g0151 | 3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1714-1194_1714-119 others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585301 | ||||||
| chr6:129585508
|
T | C | 44 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0080others(41): Show | 44 | HG00140.hp2 HG00621.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1714-1396A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585508 | ||||||
| chr6:129585620
|
G | A | 1 | a0003c0004t0005g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1714-1508C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585620 | ||||||
| chr6:129585719
|
A | T | 10 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0153others(7): Show | 10 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.1714-1607T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585719 | ||||||
| chr6:129585772
|
T | C | 4 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714-1660A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129585772 | ||||||
| chr6:129586127
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1714-2015T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129586127 | ||||||
| chr6:129586268
|
G | T | 4 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(1): Show | 4 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714-2156C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129586268 | ||||||
| chr6:129586369
|
T | C | 1 | a0001c0001t0009g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1714-2257A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129586369 | ||||||
| chr6:129586442
|
G | T | 48 | a0001c0001t0002g0057a0001c0001t0002g0066a0001c0001t0002g0068others(45): Show | 48 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1714-2330C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129586442 | ||||||
| chr6:129586452
|
G | T | 48 | a0001c0001t0002g0057a0001c0001t0002g0066a0001c0001t0002g0068others(45): Show | 48 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1714-2340C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129586452 | ||||||
| chr6:129586792
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1714-2680G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129586792 | ||||||
| chr6:129586841
|
C | T | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1714-2729G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129586841 | ||||||
| chr6:129586851
|
G | A | 5 | a0001c0001t0006g0060a0001c0001t0006g0198a0001c0001t0010g0137others(2): Show | 5 | HG02615.hp1 HG03195.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1714-2739C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129586851 | ||||||
| chr6:129587446
|
T | A | 2 | a0002c0002t0001g0033a0002c0002t0001g0041 | 2 | HG02155.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.1714-3334A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129587446 | ||||||
| chr6:129587485
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1714-3373T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129587485 | ||||||
| chr6:129587597
|
C | T | 10 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0153others(7): Show | 10 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.1714-3485G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129587597 | ||||||
| chr6:129587634
|
C | T | 2 | a0001c0001t0002g0125a0001c0001t0002g0223 | 2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1714-3522G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129587634 | ||||||
| chr6:129587967
|
G | A | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1714-3855C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129587967 | ||||||
| chr6:129587984
|
C | T | 48 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0083others(45): Show | 48 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.1714-3872G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129587984 | ||||||
| chr6:129588087
|
A | G | 141 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(138): Show | 141 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1714-3975T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588087 | ||||||
| chr6:129588095
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1714-3983C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588095 | ||||||
| chr6:129588121
|
C | CT | 47 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0083others(44): Show | 47 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1714-4010dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588121 | ||||||
| chr6:129588121
|
C | CTTT | 78 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0072others(75): Show | 78 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.1714-4012_1714-401 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588121 | ||||||
| chr6:129588195
|
A | G | 71 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076others(68): Show | 71 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.1714-4083T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588195 | ||||||
| chr6:129588213
|
G | T | 1 | a0001c0001t0001g0115 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1714-4101C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588213 | ||||||
| chr6:129588225
|
C | A | 4 | a0001c0001t0001g0126a0001c0001t0002g0125a0001c0001t0002g0223others(1): Show | 4 | HG02257.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714-4113G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588225 | ||||||
| chr6:129588242
|
C | T | 1 | a0001c0001t0009g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1714-4130G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588242 | ||||||
| chr6:129588263
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1714-4151C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588263 | ||||||
| chr6:129588371
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1714-4259G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588371 | ||||||
| chr6:129588383
|
T | C | 12 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0153others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1714-4271A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588383 | ||||||
| chr6:129588409
|
C | T | 30 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076others(27): Show | 30 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.1714-4297G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588409 | ||||||
| chr6:129588454
|
T | TCCA | 11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0153others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1714-4345_1714-434 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588454 | ||||||
| chr6:129588558
|
C | T | 69 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076others(66): Show | 69 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1714-4446G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588558 | ||||||
| chr6:129588567
|
G | A | 12 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0153others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1714-4455C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588567 | ||||||
| chr6:129588634
|
G | T | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1714-4522C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588634 | ||||||
| chr6:129588675
|
G | C | 1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1714-4563C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588675 | ||||||
| chr6:129588826
|
G | A | 2 | a0001c0001t0010g0137a0001c0011t0001g0056 | 2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1714-4714C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129588826 | ||||||
| chr6:129589223
|
T | C | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(5): Show | 8 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714-5111A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129589223 | ||||||
| chr6:129589245
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1714-5133T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129589245 | ||||||
| chr6:129589535
|
G | A | 128 | a0001c0001t0001g0065a0001c0001t0001g0072a0001c0001t0001g0073others(125): Show | 128 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1714-5423C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129589535 | ||||||
| chr6:129589677
|
T | C | 47 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0083others(44): Show | 47 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1714-5565A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129589677 | ||||||
| chr6:129589943
|
G | C | 1 | a0001c0001t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1714-5831C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129589943 | ||||||
| chr6:129589997
|
C | A | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1714-5885G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129589997 | ||||||
| chr6:129590024
|
T | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1714-5912A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590024 | ||||||
| chr6:129590276
|
C | G | 3 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139 | 3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1714-6164G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590276 | ||||||
| chr6:129590379
|
A | C | 1 | a0001c0001t0002g0162 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1714-6267T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590379 | ||||||
| chr6:129590393
|
A | C | 1 | a0001c0001t0003g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1714-6281T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590393 | ||||||
| chr6:129590394
|
T | C | 1 | a0003c0004t0005g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1714-6282A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590394 | ||||||
| chr6:129590491
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1714-6379C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590491 | ||||||
| chr6:129590644
|
C | T | 1 | a0002c0002t0002g0046 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1714-6532G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590644 | ||||||
| chr6:129590657
|
G | T | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1714-6545C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590657 | ||||||
| chr6:129590693
|
T | G | 1 | a0001c0003t0002g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1714-6581A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590693 | ||||||
| chr6:129590775
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1714-6663G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590775 | ||||||
| chr6:129590786
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1714-6674G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590786 | ||||||
| chr6:129590860
|
T | C | 19 | a0001c0001t0003g0075a0001c0001t0003g0128a0001c0001t0003g0133others(16): Show | 19 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.1714-6748A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590860 | ||||||
| chr6:129590916
|
A | G | 5 | a0001c0001t0001g0102a0001c0001t0001g0147a0001c0001t0001g0193others(2): Show | 5 | NA18950.hp2 NA18956.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.1714-6804T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590916 | ||||||
| chr6:129590917
|
A | G | 2 | a0001c0001t0010g0137a0001c0011t0001g0056 | 2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1714-6805T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590917 | ||||||
| chr6:129590920
|
T | G | 1 | a0001c0001t0001g0234 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1714-6808A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590920 | ||||||
| chr6:129590928
|
C | A | 9 | a0001c0001t0003g0075a0001c0001t0003g0219a0001c0001t0003g0222others(6): Show | 9 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.1714-6816G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129590928 | ||||||
| chr6:129591067
|
A | G | 1 | a0002c0002t0001g0038 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1714-6955T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591067 | ||||||
| chr6:129591142
|
G | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1714-7030C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591142 | ||||||
| chr6:129591268
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1714-7156A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591268 | ||||||
| chr6:129591318
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1714-7206G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591318 | ||||||
| chr6:129591369
|
G | C | 67 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076others(64): Show | 67 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1714-7257C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591369 | ||||||
| chr6:129591636
|
C | T | 69 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076others(66): Show | 69 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1714-7524G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591636 | ||||||
| chr6:129591654
|
A | G | 10 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0153others(7): Show | 10 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.1714-7542T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591654 | ||||||
| chr6:129591685
|
G | A | 1 | a0003c0004t0005g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1713+7531C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591685 | ||||||
| chr6:129591917
|
G | T | 3 | a0001c0001t0001g0079a0001c0001t0001g0136a0003c0004t0001g0151 | 3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1713+7299C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591917 | ||||||
| chr6:129591942
|
G | A | 69 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076others(66): Show | 69 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1713+7274C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129591942 | ||||||
| chr6:129592100
|
AT | A | 47 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0086others(44): Show | 47 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1713+7115delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129592100 | ||||||
| chr6:129592282
|
A | G | 69 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076others(66): Show | 69 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1713+6934T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129592282 | ||||||
| chr6:129592349
|
G | T | 1 | a0001c0001t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1713+6867C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129592349 | ||||||
| chr6:129592390
|
C | G | 2 | a0001c0001t0010g0137a0001c0011t0001g0056 | 2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1713+6826G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129592390 | ||||||
| chr6:129592503
|
G | T | 1 | a0001c0001t0003g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1713+6713C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129592503 | ||||||
| chr6:129592923
|
G | A | 67 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076others(64): Show | 67 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1713+6293C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129592923 | ||||||
| chr6:129593239
|
C | T | 65 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076others(62): Show | 65 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.1713+5977G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129593239 | ||||||
| chr6:129593697
|
T | C | 2 | a0001c0001t0010g0137a0001c0011t0001g0056 | 2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1713+5519A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129593697 | ||||||
| chr6:129593749
|
T | C | 3 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139 | 3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1713+5467A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129593749 | ||||||
| chr6:129593780
|
T | G | 2 | a0001c0001t0010g0137a0001c0011t0001g0056 | 2 | HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1713+5436A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129593780 | ||||||
| chr6:129593859
|
C | T | 1 | a0001c0001t0005g0207 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1713+5357G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129593859 | ||||||
| chr6:129594262
|
T | C | 139 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(136): Show | 139 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.1713+4954A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129594262 | ||||||
| chr6:129594726
|
T | G | 1 | a0001c0001t0001g0234 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1713+4490A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129594726 | ||||||
| chr6:129594775
|
T | C | 1 | a0002c0002t0001g0054 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1713+4441A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129594775 | ||||||
| chr6:129594800
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1713+4416C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129594800 | ||||||
| chr6:129594869
|
C | A | 19 | a0001c0001t0003g0075a0001c0001t0003g0128a0001c0001t0003g0133others(16): Show | 19 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.1713+4347G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129594869 | ||||||
| chr6:129595138
|
C | CAT | 142 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(139): Show | 142 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.1713+4077_1713+407 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129595138 | ||||||
| chr6:129595198
|
T | C | 1 | a0002c0002t0001g0014 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1713+4018A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129595198 | ||||||
| chr6:129595325
|
G | A | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1713+3891C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129595325 | ||||||
| chr6:129595459
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1713+3757C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129595459 | ||||||
| chr6:129595541
|
T | G | 20 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0080others(17): Show | 20 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.1713+3675A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129595541 | ||||||
| chr6:129595597
|
T | G | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1713+3619A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129595597 | ||||||
| chr6:129596026
|
T | C | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1713+3190A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129596026 | ||||||
| chr6:129596117
|
T | C | 3 | a0001c0001t0001g0159a0001c0001t0002g0181a0001c0001t0002g0220 | 3 | HG02071.hp1 NA18944.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.1713+3099A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129596117 | ||||||
| chr6:129596279
|
A | T | 1 | a0001c0001t0001g0099 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1713+2937T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129596279 | ||||||
| chr6:129596320
|
C | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0194 | 2 | HG02896.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1713+2896G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129596320 | ||||||
| chr6:129596506
|
C | T | 2 | a0001c0001t0001g0102a0002c0002t0001g0048 | 2 | NA18969.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1713+2710G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129596506 | ||||||
| chr6:129597058
|
T | A | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1713+2158A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597058 | ||||||
| chr6:129597094
|
C | T | 34 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0142others(31): Show | 34 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1713+2122G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597094 | ||||||
| chr6:129597126
|
T | A | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1713+2090A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597126 | ||||||
| chr6:129597127
|
A | T | 1 | a0001c0001t0001g0169 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1713+2089T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597127 | ||||||
| chr6:129597135
|
G | A | 5 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(2): Show | 5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1713+2081C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597135 | ||||||
| chr6:129597148
|
A | AT | 16 | a0001c0001t0001g0090a0001c0001t0001g0100a0001c0001t0001g0101others(13): Show | 16 | HG01192.hp2 HG01361.hp2 HG01981.hp2 others(13): Show |
intron_variant | MODIFIER | c.1713+2067dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597148 | ||||||
| chr6:129597207
|
G | A | 3 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139 | 3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1713+2009C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597207 | ||||||
| chr6:129597239
|
C | T | 4 | a0001c0001t0001g0126a0001c0001t0002g0125a0001c0001t0002g0223others(1): Show | 4 | HG02257.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1713+1977G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597239 | ||||||
| chr6:129597293
|
G | A | 3 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139 | 3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1713+1923C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597293 | ||||||
| chr6:129597400
|
T | C | 1 | a0001c0001t0001g0102 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1713+1816A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597400 | ||||||
| chr6:129597527
|
C | T | 1 | a0002c0002t0018g0009 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1713+1689G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597527 | ||||||
| chr6:129597543
|
C | T | 2 | a0001c0001t0001g0124a0001c0001t0002g0145 | 2 | HG02451.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1713+1673G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597543 | ||||||
| chr6:129597598
|
C | T | 44 | a0001c0001t0001g0065a0001c0001t0001g0074a0001c0001t0001g0086others(41): Show | 44 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1713+1618G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597598 | ||||||
| chr6:129597711
|
T | C | 1 | a0001c0001t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1713+1505A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597711 | ||||||
| chr6:129597721
|
A | G | 33 | a0001c0001t0001g0065a0001c0001t0001g0094a0001c0001t0001g0096others(30): Show | 33 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1713+1495T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597721 | ||||||
| chr6:129597730
|
G | GA | 30 | a0001c0001t0001g0065a0001c0001t0001g0094a0001c0001t0001g0098others(27): Show | 30 | HG00544.hp2 HG00738.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.1713+1485dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597730 | ||||||
| chr6:129597782
|
A | G | 33 | a0001c0001t0001g0065a0001c0001t0001g0094a0001c0001t0001g0096others(30): Show | 33 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.1713+1434T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597782 | ||||||
| chr6:129597865
|
T | C | 31 | a0001c0001t0001g0065a0001c0001t0001g0094a0001c0001t0001g0096others(28): Show | 31 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1713+1351A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597865 | ||||||
| chr6:129597905
|
A | C | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1713+1311T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597905 | ||||||
| chr6:129597908
|
A | T | 11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1713+1308T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129597908 | ||||||
| chr6:129598161
|
C | CA | 11 | a0001c0001t0001g0231a0001c0001t0002g0145a0001c0001t0003g0224others(8): Show | 11 | HG00597.hp2 HG01106.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1713+1054dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129598161 | ||||||
| chr6:129598188
|
T | C | 7 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(4): Show | 7 | HG00597.hp2 HG03130.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1713+1028A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129598188 | ||||||
| chr6:129598281
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1713+935A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129598281 | ||||||
| chr6:129598378
|
C | T | 30 | a0001c0001t0001g0065a0001c0001t0001g0094a0001c0001t0001g0096others(27): Show | 30 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.1713+838G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129598378 | ||||||
| chr6:129598630
|
A | G | 3 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139 | 3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1713+586T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129598630 | ||||||
| chr6:129598941
|
G | GGTGTGT | 30 | a0001c0001t0001g0065a0001c0001t0001g0094a0001c0001t0001g0096others(27): Show | 30 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.1713+269_1713+274d others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129598941 | ||||||
| chr6:129598946
|
G | C | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1713+270C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129598946 | ||||||
| chr6:129599153
|
AAATTTTG others(16): Show |
A | 12 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1713+40_1713+62del others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | 129599153 | ||||||
| chr6:129599360
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | splice_region_variant&intron_variant | LOW | c.1573-4A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129599360 | ||||||
| chr6:129599399
|
C | T | 3 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139 | 3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1573-43G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129599399 | ||||||
| chr6:129599431
|
T | G | 1 | a0001c0001t0002g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1573-75A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129599431 | ||||||
| chr6:129599632
|
G | A | 12 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0098others(9): Show | 12 | HG00733.hp1 HG00738.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1573-276C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129599632 | ||||||
| chr6:129599639
|
A | G | 31 | a0001c0001t0001g0065a0001c0001t0001g0094a0001c0001t0001g0096others(28): Show | 31 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1573-283T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129599639 | ||||||
| chr6:129600034
|
T | C | 1 | a0002c0002t0001g0016 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1572+608A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129600034 | ||||||
| chr6:129600071
|
G | A | 58 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(55): Show | 58 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1572+571C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129600071 | ||||||
| chr6:129600172
|
T | G | 1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1572+470A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129600172 | ||||||
| chr6:129600203
|
C | T | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1572+439G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129600203 | ||||||
| chr6:129600220
|
C | T | 9 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(6): Show | 9 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1572+422G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129600220 | ||||||
| chr6:129600433
|
G | A | 8 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0007g0077others(5): Show | 8 | HG00597.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1572+209C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129600433 | ||||||
| chr6:129600534
|
T | C | 2 | a0001c0001t0002g0229a0001c0001t0002g0230 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1572+108A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129600534 | ||||||
| chr6:129600626
|
T | C | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(5): Show | 8 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1572+16A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 11/14 | chr6 | 129600626 | ||||||
| chr6:129601088
|
C | A | 3 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139 | 3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1366-240G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601088 | ||||||
| chr6:129601098
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0136a0003c0004t0001g0151 | 3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1366-250C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601098 | ||||||
| chr6:129601105
|
G | A | 1 | a0001c0001t0003g0133 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1366-257C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601105 | ||||||
| chr6:129601107
|
G | C | 3 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139 | 3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1366-259C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601107 | ||||||
| chr6:129601190
|
C | A | 4 | a0001c0001t0001g0199a0001c0001t0001g0203a0002c0002t0001g0004others(1): Show | 4 | HG00642.hp2 HG01074.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1366-342G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601190 | ||||||
| chr6:129601368
|
G | C | 9 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(6): Show | 9 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1366-520C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601368 | ||||||
| chr6:129601469
|
A | C | 1 | a0009c0007t0001g0030 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1366-621T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601469 | ||||||
| chr6:129601506
|
AAGAGAAA others(9): Show |
A | 1 | a0001c0001t0001g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1366-674_1366-659d others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601506 | ||||||
| chr6:129601535
|
GAAGAAAA others(5): Show |
G | 5 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(2): Show | 5 | HG02615.hp2 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1366-699_1366-688d others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601535 | ||||||
| chr6:129601598
|
C | T | 3 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139 | 3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1366-750G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601598 | ||||||
| chr6:129601631
|
C | CT | 59 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(56): Show | 59 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1366-784dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601631 | ||||||
| chr6:129601721
|
G | A | 12 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1366-873C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601721 | ||||||
| chr6:129601754
|
G | A | 12 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1366-906C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601754 | ||||||
| chr6:129601808
|
CAT | C | 3 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139 | 3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1366-962_1366-961d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601808 | ||||||
| chr6:129601810
|
T | C | 1 | a0002c0002t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1366-962A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601810 | ||||||
| chr6:129601824
|
C | T | 57 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(54): Show | 57 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.1366-976G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601824 | ||||||
| chr6:129601942
|
T | A | 1 | a0001c0001t0003g0226 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1366-1094A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129601942 | ||||||
| chr6:129602036
|
C | G | 2 | a0001c0001t0001g0160a0001c0001t0001g0221 | 2 | HG02056.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1366-1188G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602036 | ||||||
| chr6:129602159
|
G | A | 1 | a0001c0001t0010g0137 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1366-1311C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602159 | ||||||
| chr6:129602276
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1366-1428T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602276 | ||||||
| chr6:129602311
|
T | C | 10 | a0001c0001t0002g0125a0001c0001t0002g0223a0001c0001t0003g0128others(7): Show | 10 | HG02257.hp2 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1366-1463A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602311 | ||||||
| chr6:129602407
|
A | C | 59 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(56): Show | 59 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.1366-1559T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602407 | ||||||
| chr6:129602419
|
C | G | 2 | a0001c0001t0001g0105a0009c0007t0001g0030 | 2 | NA19056.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1366-1571G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602419 | ||||||
| chr6:129602495
|
G | GA | 46 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(43): Show | 46 | HG00099.hp2 HG00544.hp2 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.1366-1648dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602495 | ||||||
| chr6:129602517
|
C | T | 1 | a0001c0001t0005g0212 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1366-1669G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602517 | ||||||
| chr6:129602608
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1366-1760T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602608 | ||||||
| chr6:129602709
|
T | G | 1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1366-1861A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602709 | ||||||
| chr6:129602964
|
T | C | 31 | a0001c0001t0001g0065a0001c0001t0001g0094a0001c0001t0001g0096others(28): Show | 31 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1366-2116A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602964 | ||||||
| chr6:129602987
|
T | TTA | 86 | a0001c0001t0001g0065a0001c0001t0001g0072a0001c0001t0001g0073others(83): Show | 86 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1366-2141_1366-214 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602987 | ||||||
| chr6:129602987
|
T | TTATA | 22 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.1366-2143_1366-214 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602987 | ||||||
| chr6:129602987
|
T | TTATATAT others(1): Show |
7 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(4): Show | 7 | HG00597.hp2 HG02615.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366-2147_1366-214 others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602987 | ||||||
| chr6:129602987
|
T | TTATATAT others(3): Show |
2 | a0001c0001t0001g0079a0001c0001t0001g0136 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1366-2149_1366-214 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602987 | ||||||
| chr6:129602987
|
T | TTATATAT others(5): Show |
7 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(4): Show | 7 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.1366-2151_1366-214 others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602987 | ||||||
| chr6:129602987
|
T | TTATATAT others(7): Show |
2 | a0001c0001t0006g0060a0003c0004t0001g0151 | 2 | HG03098.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1366-2153_1366-214 others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129602987 | ||||||
| chr6:129603032
|
G | A | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1366-2184C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603032 | ||||||
| chr6:129603058
|
T | C | 2 | a0001c0001t0002g0125a0001c0001t0002g0223 | 2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1366-2210A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603058 | ||||||
| chr6:129603062
|
C | T | 58 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(55): Show | 58 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1366-2214G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603062 | ||||||
| chr6:129603161
|
G | A | 1 | a0001c0001t0003g0133 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1366-2313C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603161 | ||||||
| chr6:129603261
|
G | C | 31 | a0001c0001t0001g0065a0001c0001t0001g0094a0001c0001t0001g0096others(28): Show | 31 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.1366-2413C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603261 | ||||||
| chr6:129603326
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1366-2478A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603326 | ||||||
| chr6:129603574
|
T | C | 3 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139 | 3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1365+2303A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603574 | ||||||
| chr6:129603717
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1365+2160G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603717 | ||||||
| chr6:129603858
|
A | G | 23 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0080others(20): Show | 23 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.1365+2019T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603858 | ||||||
| chr6:129603945
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0136a0003c0004t0001g0151 | 3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1365+1932C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603945 | ||||||
| chr6:129603998
|
A | T | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1365+1879T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129603998 | ||||||
| chr6:129604202
|
TC | T | 93 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(90): Show | 93 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.1365+1674delG | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129604202 | ||||||
| chr6:129604303
|
A | G | 10 | a0001c0001t0001g0216a0001c0001t0001g0218a0001c0001t0003g0219others(7): Show | 10 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.1365+1574T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129604303 | ||||||
| chr6:129604334
|
C | T | 64 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(61): Show | 64 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1365+1543G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129604334 | ||||||
| chr6:129604833
|
C | T | 29 | a0001c0001t0001g0065a0001c0001t0001g0094a0001c0001t0001g0096others(26): Show | 29 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1365+1044G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129604833 | ||||||
| chr6:129605395
|
T | G | 1 | a0001c0001t0004g0139 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1365+482A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605395 | ||||||
| chr6:129605572
|
A | G | 1 | a0001c0001t0002g0125 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1365+305T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605572 | ||||||
| chr6:129605578
|
A | G | 1 | a0001c0001t0017g0174 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1365+299T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605578 | ||||||
| chr6:129605619
|
C | T | 12 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1365+258G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605619 | ||||||
| chr6:129605620
|
G | A | 1 | a0001c0001t0001g0187 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1365+257C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605620 | ||||||
| chr6:129605624
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1365+253T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605624 | ||||||
| chr6:129605625
|
A | T | 2 | a0001c0001t0003g0224a0001c0001t0010g0137 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1365+252T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605625 | ||||||
| chr6:129605657
|
T | C | 30 | a0001c0001t0001g0065a0001c0001t0001g0094a0001c0001t0001g0096others(27): Show | 30 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.1365+220A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605657 | ||||||
| chr6:129605719
|
A | G | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1365+158T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605719 | ||||||
| chr6:129605764
|
T | C | 3 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139 | 3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1365+113A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605764 | ||||||
| chr6:129605766
|
T | C | 1 | a0001c0001t0001g0084 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1365+111A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605766 | ||||||
| chr6:129605869
|
A | G | 123 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(120): Show | 123 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(120): Show |
splice_region_variant&intron_variant | LOW | c.1365+8T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | 129605869 | ||||||
| chr6:129606065
|
G | A | 1 | a0001c0001t0002g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1283-106C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129606065 | ||||||
| chr6:129606200
|
G | A | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1283-241C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129606200 | ||||||
| chr6:129606296
|
T | G | 1 | a0001c0001t0003g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1283-337A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129606296 | ||||||
| chr6:129606459
|
C | T | 11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1283-500G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129606459 | ||||||
| chr6:129606493
|
ATTATCAT others(5): Show |
A | 3 | a0001c0001t0001g0079a0001c0001t0001g0136a0003c0004t0001g0151 | 3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1283-546_1283-535d others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129606493 | ||||||
| chr6:129606774
|
C | T | 7 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(4): Show | 7 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1283-815G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129606774 | ||||||
| chr6:129606865
|
C | CT | 39 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(36): Show | 39 | HG00099.hp2 HG00544.hp2 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.1283-907dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129606865 | ||||||
| chr6:129607116
|
T | C | 17 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(14): Show | 17 | HG00099.hp2 HG00597.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1282+777A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129607116 | ||||||
| chr6:129607373
|
A | G | 1 | a0001c0001t0013g0119 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1282+520T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129607373 | ||||||
| chr6:129607407
|
C | G | 29 | a0001c0001t0001g0065a0001c0001t0001g0094a0001c0001t0001g0096others(26): Show | 29 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1282+486G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129607407 | ||||||
| chr6:129607450
|
A | G | 6 | a0001c0001t0001g0079a0001c0001t0001g0136a0001c0001t0004g0123others(3): Show | 6 | HG02486.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1282+443T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129607450 | ||||||
| chr6:129607593
|
CTATTA | C | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(5): Show | 8 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1282+295_1282+299d others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 9/14 | chr6 | 129607593 | ||||||
| chr6:129608063
|
C | A | 2 | a0001c0001t0006g0198a0002c0002t0006g0032 | 2 | HG03491.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1123-11G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608063 | ||||||
| chr6:129608064
|
G | GA | 13 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0067others(10): Show | 13 | HG00140.hp1 HG00544.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1123-13dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608064 | ||||||
| chr6:129608064
|
G | GAAAA | 10 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0153others(7): Show | 10 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.1123-16_1123-13dup others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608064 | ||||||
| chr6:129608064
|
GA | G | 56 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0079others(53): Show | 56 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1123-13delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608064 | ||||||
| chr6:129608064
|
GAA | G | 27 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076others(24): Show | 27 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.1123-14_1123-13del others(2): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608064 | ||||||
| chr6:129608068
|
AAAAAAAA others(26): Show |
A | 1 | a0001c0001t0002g0066 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1123-49_1123-17del others(33): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608068 | ||||||
| chr6:129608084
|
A | G | 1 | a0001c0001t0002g0176 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1123-32T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608084 | ||||||
| chr6:129608088
|
A | C | 7 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(4): Show | 7 | HG00597.hp2 HG01261.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.1123-36T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608088 | ||||||
| chr6:129608124
|
T | C | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1123-72A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608124 | ||||||
| chr6:129608319
|
T | A | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1123-267A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608319 | ||||||
| chr6:129608376
|
C | T | 24 | a0001c0001t0001g0065a0001c0001t0001g0094a0001c0001t0001g0102others(21): Show | 24 | HG00544.hp2 HG01071.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1123-324G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608376 | ||||||
| chr6:129608401
|
G | A | 24 | a0001c0001t0001g0065a0001c0001t0001g0094a0001c0001t0001g0102others(21): Show | 24 | HG00544.hp2 HG01071.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1123-349C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608401 | ||||||
| chr6:129608417
|
A | C | 1 | a0002c0002t0001g0016 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1123-365T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608417 | ||||||
| chr6:129608433
|
G | A | 1 | a0001c0001t0003g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1123-381C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608433 | ||||||
| chr6:129608743
|
A | G | 12 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.1123-691T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608743 | ||||||
| chr6:129608898
|
C | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0136a0003c0004t0001g0151 | 3 | HG02486.hp1 HG03098.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1123-846G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608898 | ||||||
| chr6:129608966
|
TAGAG | T | 11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1123-918_1123-915d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129608966 | ||||||
| chr6:129609005
|
GA | G | 24 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076others(21): Show | 24 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1123-954delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609005 | ||||||
| chr6:129609071
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1123-1019C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609071 | ||||||
| chr6:129609104
|
GGGGAAAG others(8): Show |
G | 1 | a0001c0001t0002g0173 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1123-1067_1123-105 others(19): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609104 | ||||||
| chr6:129609202
|
T | C | 1 | a0001c0001t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1123-1150A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609202 | ||||||
| chr6:129609451
|
G | A | 58 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(55): Show | 58 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1123-1399C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609451 | ||||||
| chr6:129609459
|
T | C | 18 | a0001c0001t0001g0074a0001c0001t0001g0083a0001c0001t0001g0086others(15): Show | 18 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.1123-1407A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609459 | ||||||
| chr6:129609501
|
T | C | 25 | a0001c0001t0001g0142a0001c0001t0001g0216a0001c0001t0001g0218others(22): Show | 25 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.1123-1449A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609501 | ||||||
| chr6:129609509
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1123-1457G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609509 | ||||||
| chr6:129609573
|
TGTTACCT others(407): Show |
T | 1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1122+1546_1123-152 others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609573 | ||||||
| chr6:129609599
|
C | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0140 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1123-1547G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609599 | ||||||
| chr6:129609629
|
G | A | 3 | a0001c0001t0001g0096a0001c0001t0001g0178a0002c0002t0001g0010 | 3 | HG00733.hp1 HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1123-1577C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609629 | ||||||
| chr6:129609654
|
A | G | 1 | a0002c0002t0001g0026 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1123-1602T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609654 | ||||||
| chr6:129609734
|
G | C | 4 | a0001c0001t0001g0079a0001c0001t0001g0136a0003c0004t0001g0151others(1): Show | 4 | HG02486.hp1 HG03098.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1123-1682C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609734 | ||||||
| chr6:129609765
|
C | T | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1123-1713G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609765 | ||||||
| chr6:129609964
|
G | T | 1 | a0001c0001t0001g0116 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1122+1569C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129609964 | ||||||
| chr6:129610057
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1122+1476G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129610057 | ||||||
| chr6:129610201
|
C | T | 1 | a0005c0012t0002g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1122+1332G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129610201 | ||||||
| chr6:129610236
|
C | G | 13 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(10): Show | 13 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.1122+1297G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129610236 | ||||||
| chr6:129610334
|
C | T | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1122+1199G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129610334 | ||||||
| chr6:129610442
|
C | T | 1 | a0001c0001t0002g0162 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1122+1091G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129610442 | ||||||
| chr6:129610494
|
T | C | 1 | a0002c0002t0002g0050 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1122+1039A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129610494 | ||||||
| chr6:129610727
|
A | C | 1 | a0001c0001t0001g0200 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1122+806T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129610727 | ||||||
| chr6:129610788
|
T | C | 38 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0079others(35): Show | 38 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.1122+745A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129610788 | ||||||
| chr6:129610962
|
T | C | 29 | a0001c0001t0001g0065a0001c0001t0001g0094a0001c0001t0001g0096others(26): Show | 29 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.1122+571A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129610962 | ||||||
| chr6:129611058
|
G | A | 13 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(10): Show | 13 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1122+475C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129611058 | ||||||
| chr6:129611503
|
A | C | 11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1122+30T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | 129611503 | ||||||
| chr6:129611642
|
C | T | 1 | a0002c0002t0001g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1045-32G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129611642 | ||||||
| chr6:129611643
|
G | A | 3 | a0001c0001t0002g0145a0001c0001t0010g0137a0003c0004t0005g0088 | 3 | HG02451.hp1 HG03195.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1045-33C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129611643 | ||||||
| chr6:129611703
|
T | C | 6 | a0001c0001t0001g0079a0001c0001t0001g0136a0001c0001t0004g0123others(3): Show | 6 | HG02486.hp1 HG02622.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1045-93A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129611703 | ||||||
| chr6:129611749
|
T | C | 100 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(97): Show | 100 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1045-139A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129611749 | ||||||
| chr6:129611839
|
T | C | 62 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(59): Show | 62 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1045-229A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129611839 | ||||||
| chr6:129612438
|
A | C | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1045-828T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129612438 | ||||||
| chr6:129612661
|
T | C | 2 | a0001c0001t0002g0184a0001c0001t0003g0183 | 2 | NA18990.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1045-1051A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129612661 | ||||||
| chr6:129612727
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0136 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1045-1117T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129612727 | ||||||
| chr6:129612736
|
T | C | 4 | a0001c0001t0001g0079a0001c0001t0001g0136a0001c0001t0002g0145others(1): Show | 4 | HG02451.hp1 HG02486.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1045-1126A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129612736 | ||||||
| chr6:129612944
|
C | G | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1045-1334G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129612944 | ||||||
| chr6:129612998
|
G | C | 1 | a0002c0002t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1045-1388C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129612998 | ||||||
| chr6:129613004
|
C | T | 3 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139 | 3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1045-1394G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613004 | ||||||
| chr6:129613005
|
G | A | 11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1045-1395C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613005 | ||||||
| chr6:129613032
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1045-1422C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613032 | ||||||
| chr6:129613042
|
G | C | 2 | a0001c0001t0001g0126a0002c0002t0001g0025 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1045-1432C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613042 | ||||||
| chr6:129613158
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1045-1548G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613158 | ||||||
| chr6:129613159
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(127): Show | 131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1045-1549T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613159 | ||||||
| chr6:129613164
|
C | T | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1045-1554G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613164 | ||||||
| chr6:129613182
|
A | G | 1 | a0002c0002t0001g0040 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1045-1572T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613182 | ||||||
| chr6:129613194
|
G | C | 25 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0108others(22): Show | 25 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1045-1584C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613194 | ||||||
| chr6:129613232
|
C | CA | 49 | a0001c0001t0001g0001a0001c0001t0001g0065a0001c0001t0001g0090others(46): Show | 50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1045-1623dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613232 | ||||||
| chr6:129613232
|
CA | C | 27 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0089others(24): Show | 27 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.1045-1623delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613232 | ||||||
| chr6:129613280
|
C | T | 1 | a0001c0001t0001g0196 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1045-1670G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613280 | ||||||
| chr6:129613335
|
C | T | 10 | a0001c0001t0002g0145a0001c0001t0005g0207a0001c0001t0005g0212others(7): Show | 10 | HG00597.hp2 HG02451.hp1 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.1045-1725G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613335 | ||||||
| chr6:129613493
|
T | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1045-1883A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613493 | ||||||
| chr6:129613650
|
C | T | 11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1045-2040G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613650 | ||||||
| chr6:129613790
|
G | T | 3 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139 | 3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1045-2180C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613790 | ||||||
| chr6:129613825
|
C | T | 1 | a0002c0002t0002g0019 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1045-2215G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613825 | ||||||
| chr6:129613844
|
G | GTTT | 25 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0108others(22): Show | 25 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1045-2235_1045-223 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613844 | ||||||
| chr6:129613952
|
CTT | C | 3 | a0001c0001t0001g0108a0001c0001t0001g0191a0002c0002t0018g0009 | 3 | HG00140.hp2 HG00639.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.1044+2258_1044+225 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129613952 | ||||||
| chr6:129614177
|
G | A | 5 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(2): Show | 5 | HG00597.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1044+2035C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614177 | ||||||
| chr6:129614230
|
C | A | 4 | a0001c0001t0001g0079a0001c0001t0001g0136a0001c0001t0007g0077others(1): Show | 4 | HG02486.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1044+1982G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614230 | ||||||
| chr6:129614291
|
T | C | 25 | a0001c0001t0001g0142a0001c0001t0001g0216a0001c0001t0001g0218others(22): Show | 25 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.1044+1921A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614291 | ||||||
| chr6:129614417
|
T | A | 11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.1044+1795A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614417 | ||||||
| chr6:129614465
|
T | C | 25 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0108others(22): Show | 25 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.1044+1747A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614465 | ||||||
| chr6:129614468
|
A | G | 2 | a0003c0004t0001g0151a0003c0004t0005g0088 | 2 | HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1044+1744T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614468 | ||||||
| chr6:129614748
|
A | AT | 13 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076others(10): Show | 13 | HG00609.hp1 HG01081.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.1044+1463dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614748 | ||||||
| chr6:129614748
|
AT | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0064others(67): Show | 71 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.1044+1463delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614748 | ||||||
| chr6:129614748
|
ATT | A | 27 | a0001c0001t0001g0112a0001c0001t0001g0142a0001c0001t0001g0216others(24): Show | 27 | HG00408.hp2 HG00558.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1044+1462_1044+146 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614748 | ||||||
| chr6:129614748
|
ATTT | A | 6 | a0001c0001t0003g0225a0001c0001t0005g0207a0001c0001t0005g0212others(3): Show | 6 | HG00597.hp2 HG02630.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.1044+1461_1044+146 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614748 | ||||||
| chr6:129614816
|
T | C | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1044+1396A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614816 | ||||||
| chr6:129614880
|
G | A | 26 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0091others(23): Show | 26 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.1044+1332C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129614880 | ||||||
| chr6:129615007
|
A | T | 1 | a0001c0001t0001g0177 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1044+1205T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615007 | ||||||
| chr6:129615078
|
T | G | 1 | a0001c0001t0001g0164 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1044+1134A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615078 | ||||||
| chr6:129615245
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1044+967C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615245 | ||||||
| chr6:129615417
|
C | T | 5 | a0001c0001t0001g0100a0001c0001t0001g0106a0001c0001t0001g0107others(2): Show | 5 | NA18950.hp1 NA18977.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.1044+795G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615417 | ||||||
| chr6:129615433
|
G | C | 13 | a0001c0001t0001g0065a0001c0001t0001g0129a0001c0001t0001g0155others(10): Show | 13 | HG00544.hp2 HG01071.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1044+779C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615433 | ||||||
| chr6:129615470
|
A | G | 1 | a0001c0001t0001g0156 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1044+742T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615470 | ||||||
| chr6:129615532
|
G | C | 1 | a0002c0002t0001g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1044+680C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615532 | ||||||
| chr6:129615595
|
A | G | 1 | a0001c0001t0002g0227 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1044+617T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615595 | ||||||
| chr6:129615617
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1044+595G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615617 | ||||||
| chr6:129615630
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0065a0001c0001t0001g0079others(99): Show | 103 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1044+582G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615630 | ||||||
| chr6:129615668
|
G | A | 5 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(2): Show | 5 | HG00597.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1044+544C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615668 | ||||||
| chr6:129615686
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0065a0001c0001t0001g0079others(99): Show | 103 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1044+526G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615686 | ||||||
| chr6:129615744
|
C | G | 1 | a0002c0002t0001g0005 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1044+468G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615744 | ||||||
| chr6:129615881
|
G | A | 1 | a0002c0002t0002g0039 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1044+331C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615881 | ||||||
| chr6:129615892
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1044+320C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615892 | ||||||
| chr6:129615968
|
A | G | 1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1044+244T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615968 | ||||||
| chr6:129615997
|
G | T | 1 | a0001c0001t0002g0172 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1044+215C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129615997 | ||||||
| chr6:129616086
|
T | C | 1 | a0001c0001t0010g0137 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1044+126A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129616086 | ||||||
| chr6:129616144
|
T | C | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1044+68A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 7/14 | chr6 | 129616144 | ||||||
| chr6:129616311
|
A | G | 11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.953-8T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129616311 | ||||||
| chr6:129616752
|
A | T | 6 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(3): Show | 6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.953-449T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129616752 | ||||||
| chr6:129616803
|
A | G | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.953-500T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129616803 | ||||||
| chr6:129616886
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0001g0157 | 2 | HG02602.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.953-583C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129616886 | ||||||
| chr6:129617050
|
G | A | 1 | a0002c0002t0001g0038 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.953-747C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129617050 | ||||||
| chr6:129617083
|
A | G | 6 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(3): Show | 6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.953-780T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129617083 | ||||||
| chr6:129617091
|
C | A | 9 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(6): Show | 9 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.953-788G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129617091 | ||||||
| chr6:129617459
|
AATTCGGA others(13): Show |
A | 1 | a0002c0002t0001g0038 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.953-1176_953-1157d others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129617459 | ||||||
| chr6:129617635
|
G | C | 25 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0108others(22): Show | 25 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.952+1052C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129617635 | ||||||
| chr6:129617867
|
G | T | 25 | a0001c0001t0001g0142a0001c0001t0001g0216a0001c0001t0001g0218others(22): Show | 25 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.952+820C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129617867 | ||||||
| chr6:129618113
|
C | A | 1 | a0002c0002t0003g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.952+574G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129618113 | ||||||
| chr6:129618113
|
CA | C | 43 | a0001c0001t0001g0080a0001c0001t0001g0089a0001c0001t0001g0108others(40): Show | 43 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.952+573delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129618113 | ||||||
| chr6:129618114
|
A | C | 1 | a0002c0002t0003g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.952+573T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129618114 | ||||||
| chr6:129618117
|
A | C | 16 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0064others(13): Show | 17 | HG00099.hp2 HG00597.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.952+570T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129618117 | ||||||
| chr6:129618220
|
T | C | 1 | a0001c0001t0001g0106 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.952+467A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 6/14 | chr6 | 129618220 | ||||||
| chr6:129619118
|
A | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0064others(58): Show | 62 | HG00099.hp2 HG00544.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.787-266T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619118 | ||||||
| chr6:129619257
|
GA | G | 3 | a0001c0001t0003g0128a0001c0001t0003g0237a0002c0002t0014g0045 | 3 | HG02257.hp2 HG03540.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.787-406delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619257 | ||||||
| chr6:129619336
|
A | G | 1 | a0001c0001t0016g0149 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.787-484T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619336 | ||||||
| chr6:129619345
|
C | CAGGGGGA others(19): Show |
1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.787-519_787-494dup others(26): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619345 | ||||||
| chr6:129619345
|
CAGGGGGA others(6): Show |
C | 4 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(1): Show | 4 | HG02622.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-506_787-494del others(13): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619345 | ||||||
| chr6:129619368
|
GA | G | 9 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0112others(6): Show | 9 | HG00423.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.787-517delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619368 | ||||||
| chr6:129619369
|
A | AAAAGGGG others(5): Show |
9 | a0001c0001t0001g0180a0001c0001t0001g0187a0001c0001t0002g0181others(6): Show | 9 | HG00544.hp1 HG02027.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.787-529_787-518dup others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619369 | ||||||
| chr6:129619369
|
AAAAGGGG others(5): Show |
A | 25 | a0001c0001t0001g0142a0001c0001t0001g0216a0001c0001t0001g0218others(22): Show | 25 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.787-529_787-518del others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619369 | ||||||
| chr6:129619372
|
A | AGGGGGAG others(6): Show |
1 | a0001c0001t0001g0074 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.787-533_787-521dup others(13): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619372 | ||||||
| chr6:129619397
|
G | GGGGGAGG others(4): Show |
1 | a0001c0001t0001g0086 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.787-546_787-545ins others(11): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619397 | ||||||
| chr6:129619467
|
A | AGGGGGAG others(1046): Show |
1 | a0001c0001t0002g0168 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.787-616_787-615ins others(1053): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619467 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1068): Show |
1 | a0001c0001t0001g0166 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1075): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1020): Show |
1 | a0001c0001t0013g0119 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1027): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1082): Show |
1 | a0002c0002t0001g0038 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1089): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1051): Show |
2 | a0001c0001t0008g0118a0001c0001t0008g0228 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1058): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1045): Show |
1 | a0001c0001t0003g0219 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1052): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1097): Show |
1 | a0002c0002t0003g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1104): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1058): Show |
10 | a0001c0001t0001g0216a0001c0001t0001g0218a0001c0001t0002g0223others(7): Show | 10 | HG00408.hp2 HG00558.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.787-617_787-616ins others(1065): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1044): Show |
2 | a0001c0001t0003g0128a0002c0002t0014g0045 | 2 | HG03540.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1051): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1058): Show |
1 | a0002c0002t0003g0027 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1065): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1045): Show |
1 | a0001c0001t0003g0237 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1052): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1071): Show |
2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1078): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1084): Show |
2 | a0001c0001t0001g0142a0008c0005t0003g0002 | 2 | HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1091): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1078): Show |
1 | a0001c0001t0003g0226 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1085): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1078): Show |
1 | a0001c0001t0002g0125 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1085): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1069): Show |
1 | a0001c0001t0001g0121 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1076): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1024): Show |
1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1031): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1064): Show |
1 | a0001c0001t0002g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1071): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1028): Show |
1 | a0002c0002t0001g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1035): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1045): Show |
3 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0210 | 3 | NA18954.hp2 NA19000.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1052): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(997): Show |
1 | a0004c0013t0001g0208 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1004): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1065): Show |
1 | a0001c0001t0004g0139 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1072): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1045): Show |
3 | a0001c0001t0001g0124a0002c0002t0002g0028a0002c0002t0003g0029 | 3 | HG03041.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1052): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1069): Show |
1 | a0001c0001t0002g0162 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1076): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1032): Show |
1 | a0001c0001t0001g0146 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1039): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1068): Show |
1 | a0001c0001t0001g0001 | 2 | HG00738.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1075): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1079): Show |
4 | a0001c0001t0001g0199a0001c0001t0001g0203a0002c0002t0001g0004others(1): Show | 4 | HG00642.hp2 HG01074.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-617_787-616ins others(1086): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1059): Show |
1 | a0001c0001t0001g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1066): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1068): Show |
1 | a0002c0002t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1075): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1081): Show |
1 | a0001c0001t0001g0106 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1088): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1068): Show |
1 | a0002c0002t0001g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1075): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1066): Show |
1 | a0002c0002t0001g0021 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1073): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1086): Show |
2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1093): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1068): Show |
32 | a0001c0001t0001g0090a0001c0001t0001g0094a0001c0001t0001g0096others(29): Show | 32 | HG00621.hp1 HG00639.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.787-617_787-616ins others(1075): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1050): Show |
1 | a0001c0001t0001g0214 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1057): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1082): Show |
1 | a0001c0001t0001g0194 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1089): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1066): Show |
1 | a0001c0001t0004g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1073): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1067): Show |
1 | a0001c0001t0004g0123 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1074): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1068): Show |
1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1075): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1028): Show |
1 | a0001c0001t0002g0220 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1035): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1078): Show |
1 | a0002c0002t0001g0035 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1085): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1103): Show |
3 | a0001c0001t0001g0105a0002c0006t0012g0034a0009c0007t0001g0030 | 3 | NA19056.hp1 NA19056.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1110): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1172): Show |
1 | a0002c0002t0001g0049 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1179): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1051): Show |
1 | a0002c0002t0002g0046 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1058): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1024): Show |
1 | a0001c0001t0001g0130 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1031): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1032): Show |
1 | a0001c0001t0001g0148 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1039): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1019): Show |
2 | a0001c0001t0002g0092a0001c0001t0002g0176 | 2 | HG01928.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1026): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1044): Show |
1 | a0001c0001t0001g0209 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1051): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1070): Show |
1 | a0002c0002t0002g0050 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1077): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1045): Show |
26 | a0001c0001t0001g0085a0001c0001t0001g0111a0001c0001t0001g0126others(23): Show | 26 | HG00558.hp2 HG01106.hp2 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.787-617_787-616ins others(1052): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1045): Show |
5 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0163others(2): Show | 5 | HG00438.hp2 NA18942.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-617_787-616ins others(1052): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1058): Show |
1 | a0002c0002t0001g0040 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1065): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1050): Show |
1 | a0001c0001t0001g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1057): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1077): Show |
1 | a0001c0001t0001g0076 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1084): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1007): Show |
1 | a0001c0001t0002g0185 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1014): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1032): Show |
12 | a0001c0001t0001g0201a0001c0001t0001g0206a0001c0001t0001g0213others(9): Show | 12 | HG00438.hp1 HG01358.hp2 HG02132.hp2 others(9): Show |
intron_variant | MODIFIER | c.787-617_787-616ins others(1039): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1057): Show |
2 | a0001c0001t0002g0143a0001c0001t0002g0170 | 2 | HG02004.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1064): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1051): Show |
1 | a0001c0001t0002g0181 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1058): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1037): Show |
1 | a0002c0002t0001g0017 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1044): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1038): Show |
1 | a0001c0003t0002g0190 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1045): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1038): Show |
11 | a0001c0001t0001g0180a0001c0001t0001g0187a0001c0001t0002g0082others(8): Show | 11 | HG00544.hp1 HG02027.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.787-617_787-616ins others(1045): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1051): Show |
1 | a0002c0002t0001g0018 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1058): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1039): Show |
1 | a0001c0001t0001g0061 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1046): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1052): Show |
1 | a0002c0002t0001g0007 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1059): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1039): Show |
1 | a0001c0001t0001g0062 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1046): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1058): Show |
3 | a0001c0001t0002g0184a0001c0001t0003g0183a0002c0002t0002g0039 | 3 | NA18964.hp2 NA18990.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1065): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(999): Show |
7 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(4): Show | 7 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.787-617_787-616ins others(1006): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1058): Show |
2 | a0001c0001t0001g0072a0001c0001t0002g0093 | 2 | HG00609.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1065): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1006): Show |
1 | a0001c0001t0002g0152 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1013): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1062): Show |
3 | a0001c0001t0001g0112a0001c0001t0001g0140a0001c0001t0011g0141 | 3 | HG02615.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.787-617_787-616ins others(1069): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1051): Show |
1 | a0001c0001t0001g0091 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1058): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1039): Show |
1 | a0001c0001t0001g0074 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1046): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1055): Show |
1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1062): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1046): Show |
1 | a0001c0001t0001g0195 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1053): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1046): Show |
1 | a0001c0001t0001g0160 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1053): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1060): Show |
1 | a0002c0002t0001g0036 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1067): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1048): Show |
1 | a0001c0001t0016g0149 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1055): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1013): Show |
1 | a0001c0001t0001g0202 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1020): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1069): Show |
1 | a0001c0001t0001g0161 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1076): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1043): Show |
1 | a0001c0001t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1050): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1046): Show |
1 | a0001c0001t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1053): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1033): Show |
1 | a0001c0001t0001g0065 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1040): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1000): Show |
1 | a0001c0001t0001g0177 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1007): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1052): Show |
1 | a0001c0001t0002g0145 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1059): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(918): Show |
1 | a0001c0001t0001g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(925): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(777): Show |
1 | a0001c0001t0009g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(784): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1039): Show |
1 | a0001c0001t0010g0137 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1046): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1046): Show |
1 | a0001c0001t0002g0113 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1053): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(778): Show |
3 | a0001c0001t0005g0207a0001c0011t0001g0056a0002c0002t0005g0024 | 3 | HG00597.hp2 HG03209.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(785): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(907): Show |
1 | a0001c0001t0001g0153 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(914): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(920): Show |
7 | a0001c0001t0001g0080a0001c0001t0001g0109a0001c0001t0001g0157others(4): Show | 7 | HG00639.hp1 HG00642.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.787-617_787-616ins others(927): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1088): Show |
1 | a0003c0004t0005g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1095): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(765): Show |
2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.787-617_787-616ins others(772): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(779): Show |
1 | a0001c0001t0005g0212 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(786): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1101): Show |
1 | a0003c0004t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1108): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1046): Show |
1 | a0001c0001t0001g0196 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1053): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(935): Show |
1 | a0002c0002t0001g0016 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(942): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(936): Show |
1 | a0002c0002t0018g0009 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(943): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1032): Show |
1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1039): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1008): Show |
1 | a0001c0001t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1015): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(775): Show |
1 | a0001c0001t0009g0069 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(782): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1431): Show |
1 | a0001c0001t0003g0224 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1438): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1044): Show |
1 | a0002c0002t0001g0026 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1051): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1074): Show |
1 | a0001c0001t0015g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1081): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(1064): Show |
1 | a0001c0001t0003g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1071): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(945): Show |
1 | a0001c0001t0001g0136 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(952): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGAGG others(946): Show |
1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(953): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGGAG others(1040): Show |
1 | a0001c0009t0001g0122 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.787-617_787-616ins others(1047): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619468
|
G | GGGGGGAG others(1051): Show |
1 | a0001c0001t0001g0089 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.787-617_787-616ins others(1058): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619468 | ||||||
| chr6:129619469
|
G | GGGGAGGG others(1031): Show |
1 | a0001c0001t0001g0086 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.787-618_787-617ins others(1038): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619469 | ||||||
| chr6:129619479
|
A | AG | 6 | a0001c0001t0001g0064a0001c0001t0001g0074a0001c0001t0001g0096others(3): Show | 6 | HG00438.hp2 HG00597.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-628dupC | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619479 | ||||||
| chr6:129619482
|
G | A | 2 | a0001c0001t0002g0182a0001c0001t0002g0185 | 2 | HG01074.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.787-630C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619482 | ||||||
| chr6:129619488
|
C | CAG | 50 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0108others(47): Show | 50 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.787-637_787-636ins others(2): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619488 | ||||||
| chr6:129619509
|
G | A | 11 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(8): Show | 11 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.787-657C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619509 | ||||||
| chr6:129619635
|
G | A | 2 | a0003c0004t0001g0151a0003c0004t0005g0088 | 2 | HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.787-783C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619635 | ||||||
| chr6:129619665
|
A | C | 11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.787-813T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619665 | ||||||
| chr6:129619689
|
G | C | 11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.787-837C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619689 | ||||||
| chr6:129619979
|
A | AGAAG | 15 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0108others(12): Show | 15 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.787-1131_787-1128d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129619979 | ||||||
| chr6:129620027
|
C | T | 2 | a0001c0001t0001g0126a0002c0002t0001g0025 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.787-1175G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129620027 | ||||||
| chr6:129620052
|
G | A | 1 | a0001c0003t0002g0211 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.787-1200C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129620052 | ||||||
| chr6:129620702
|
C | T | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.787-1850G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129620702 | ||||||
| chr6:129620749
|
T | C | 5 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(2): Show | 5 | HG00597.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-1897A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129620749 | ||||||
| chr6:129620809
|
T | C | 1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.787-1957A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129620809 | ||||||
| chr6:129620989
|
A | G | 8 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0007g0077others(5): Show | 8 | HG00597.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.787-2137T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129620989 | ||||||
| chr6:129621018
|
T | C | 59 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(56): Show | 60 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.787-2166A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621018 | ||||||
| chr6:129621084
|
T | C | 1 | a0002c0002t0001g0017 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.787-2232A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621084 | ||||||
| chr6:129621085
|
A | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0136 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.787-2233T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621085 | ||||||
| chr6:129621278
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0136 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.787-2426C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621278 | ||||||
| chr6:129621322
|
C | G | 6 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(3): Show | 6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-2470G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621322 | ||||||
| chr6:129621328
|
A | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.787-2476T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621328 | ||||||
| chr6:129621363
|
G | A | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.787-2511C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621363 | ||||||
| chr6:129621374
|
G | GT | 8 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0001g0074others(5): Show | 8 | HG00597.hp1 HG01433.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.787-2523dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621374 | ||||||
| chr6:129621403
|
A | T | 1 | a0002c0002t0001g0026 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.787-2551T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621403 | ||||||
| chr6:129621478
|
G | T | 11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.787-2626C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621478 | ||||||
| chr6:129621625
|
T | C | 11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.787-2773A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621625 | ||||||
| chr6:129621672
|
T | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.787-2820A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621672 | ||||||
| chr6:129621696
|
A | G | 1 | a0001c0001t0013g0119 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.787-2844T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621696 | ||||||
| chr6:129621764
|
T | C | 6 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(3): Show | 6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-2912A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621764 | ||||||
| chr6:129621775
|
A | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(54): Show | 58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.787-2923T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621775 | ||||||
| chr6:129621796
|
T | A | 10 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(7): Show | 10 | HG00423.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.787-2944A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621796 | ||||||
| chr6:129621931
|
G | GT | 51 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.787-3080dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129621931 | ||||||
| chr6:129622043
|
G | T | 13 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(10): Show | 13 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.787-3191C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129622043 | ||||||
| chr6:129622159
|
T | C | 52 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(49): Show | 53 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.787-3307A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129622159 | ||||||
| chr6:129622181
|
G | C | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG01106.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.787-3329C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129622181 | ||||||
| chr6:129622250
|
A | G | 6 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(3): Show | 6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-3398T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129622250 | ||||||
| chr6:129622329
|
T | C | 5 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(2): Show | 5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.787-3477A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129622329 | ||||||
| chr6:129622716
|
T | TAAG | 57 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(54): Show | 58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.787-3867_787-3865d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129622716 | ||||||
| chr6:129622852
|
C | G | 1 | a0002c0002t0002g0020 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.787-4000G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129622852 | ||||||
| chr6:129622958
|
G | C | 1 | a0001c0001t0001g0114 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.787-4106C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129622958 | ||||||
| chr6:129623001
|
CAAAACAA others(9): Show |
C | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG00621.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.787-4165_787-4150d others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623001 | ||||||
| chr6:129623003
|
AAAC | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0096others(42): Show | 46 | HG00544.hp2 HG00639.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.787-4154_787-4152d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623003 | ||||||
| chr6:129623006
|
CA | C | 40 | a0001c0001t0001g0127a0001c0001t0001g0142a0001c0001t0001g0150others(37): Show | 40 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.787-4155delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623006 | ||||||
| chr6:129623006
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.787-4165_787-4155d others(13): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623006 | ||||||
| chr6:129623036
|
A | G | 1 | a0001c0001t0013g0119 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.787-4184T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623036 | ||||||
| chr6:129623053
|
C | CA | 26 | a0001c0001t0001g0065a0001c0001t0001g0142a0001c0001t0001g0216others(23): Show | 26 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.787-4202dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623053 | ||||||
| chr6:129623082
|
T | A | 127 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0064others(124): Show | 128 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.787-4230A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623082 | ||||||
| chr6:129623239
|
A | T | 1 | a0001c0001t0003g0224 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.787-4387T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623239 | ||||||
| chr6:129623711
|
C | CAATGAGT others(4): Show |
1 | a0001c0001t0002g0113 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.787-4870_787-4860d others(13): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623711 | ||||||
| chr6:129623979
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0136 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.787-5127A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129623979 | ||||||
| chr6:129624032
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.787-5180C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624032 | ||||||
| chr6:129624080
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.787-5228C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624080 | ||||||
| chr6:129624148
|
C | T | 1 | a0002c0002t0002g0019 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.786+5205G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624148 | ||||||
| chr6:129624372
|
T | C | 25 | a0001c0001t0001g0142a0001c0001t0001g0216a0001c0001t0001g0218others(22): Show | 25 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.786+4981A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624372 | ||||||
| chr6:129624374
|
T | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(54): Show | 58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.786+4979A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624374 | ||||||
| chr6:129624440
|
G | A | 1 | a0005c0012t0002g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.786+4913C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624440 | ||||||
| chr6:129624455
|
A | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+4898T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624455 | ||||||
| chr6:129624466
|
G | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.786+4887C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624466 | ||||||
| chr6:129624515
|
C | T | 25 | a0001c0001t0001g0142a0001c0001t0001g0216a0001c0001t0001g0218others(22): Show | 25 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.786+4838G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624515 | ||||||
| chr6:129624545
|
A | T | 2 | a0001c0001t0008g0118a0001c0001t0008g0228 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.786+4808T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624545 | ||||||
| chr6:129624592
|
T | C | 25 | a0001c0001t0001g0142a0001c0001t0001g0216a0001c0001t0001g0218others(22): Show | 25 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.786+4761A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624592 | ||||||
| chr6:129624610
|
T | A | 1 | a0001c0001t0001g0157 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.786+4743A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624610 | ||||||
| chr6:129624637
|
C | T | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4716G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624637 | ||||||
| chr6:129624673
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0080others(98): Show | 102 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.786+4680T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624673 | ||||||
| chr6:129624735
|
A | T | 1 | a0001c0001t0002g0220 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.786+4618T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624735 | ||||||
| chr6:129624736
|
G | A | 1 | a0001c0001t0002g0162 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.786+4617C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624736 | ||||||
| chr6:129624736
|
G | T | 1 | a0001c0001t0002g0220 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.786+4617C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624736 | ||||||
| chr6:129624806
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0136 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+4547C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624806 | ||||||
| chr6:129624825
|
A | T | 1 | a0003c0004t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.786+4528T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624825 | ||||||
| chr6:129624877
|
G | A | 11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.786+4476C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624877 | ||||||
| chr6:129624948
|
A | T | 1 | a0001c0001t0002g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.786+4405T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624948 | ||||||
| chr6:129624949
|
A | AAT | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(5): Show | 8 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4402_786+4403d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624949 | ||||||
| chr6:129624956
|
A | ATATATAT others(26): Show |
1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.786+4364_786+4396d others(35): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624956 | ||||||
| chr6:129624976
|
T | A | 1 | a0001c0001t0002g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.786+4377A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624976 | ||||||
| chr6:129624990
|
T | G | 19 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(16): Show | 19 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.786+4363A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624990 | ||||||
| chr6:129624990
|
T | TATATATG | 51 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.786+4356_786+4362d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624990 | ||||||
| chr6:129624990
|
T | TATATATG others(24): Show |
3 | a0001c0001t0003g0224a0002c0002t0001g0031a0002c0002t0006g0032 | 3 | HG03130.hp1 HG03491.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.786+4332_786+4362d others(33): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129624990 | ||||||
| chr6:129625002
|
A | T | 1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.786+4351T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625002 | ||||||
| chr6:129625006
|
T | TTA | 15 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(12): Show | 15 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(12): Show |
intron_variant | MODIFIER | c.786+4345_786+4346d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625006 | ||||||
| chr6:129625006
|
T | TTATATAT others(2): Show |
51 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.786+4346_786+4347i others(11): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625006 | ||||||
| chr6:129625006
|
T | TTATATAT others(28): Show |
1 | a0001c0001t0001g0136 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.786+4346_786+4347i others(37): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625006 | ||||||
| chr6:129625013
|
A | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.786+4340T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625013 | ||||||
| chr6:129625021
|
G | T | 15 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0079others(12): Show | 15 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(12): Show |
intron_variant | MODIFIER | c.786+4332C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625021 | ||||||
| chr6:129625037
|
T | TTA | 94 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0084others(91): Show | 95 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.786+4314_786+4315d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625037 | ||||||
| chr6:129625044
|
A | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+4309T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625044 | ||||||
| chr6:129625054
|
T | TATA | 95 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0064others(92): Show | 96 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.786+4298_786+4299i others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625054 | ||||||
| chr6:129625054
|
T | TATATGAT others(29): Show |
12 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.786+4298_786+4299i others(38): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625054 | ||||||
| chr6:129625055
|
T | A | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4298A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625055 | ||||||
| chr6:129625056
|
G | T | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4297C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625056 | ||||||
| chr6:129625057
|
A | G | 49 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(46): Show | 50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.786+4296T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625057 | ||||||
| chr6:129625058
|
T | TG | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4294_786+4295i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625058 | ||||||
| chr6:129625066
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.786+4287A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625066 | ||||||
| chr6:129625066
|
T | G | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4287A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625066 | ||||||
| chr6:129625072
|
TAA | T | 3 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139 | 3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.786+4279_786+4280d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625072 | ||||||
| chr6:129625073
|
A | C | 33 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0096others(30): Show | 34 | HG00621.hp1 HG00639.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.786+4280T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625073 | ||||||
| chr6:129625074
|
A | T | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4279T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625074 | ||||||
| chr6:129625075
|
TATATATG | T | 7 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(4): Show | 7 | HG00597.hp2 HG02818.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.786+4271_786+4277d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625075 | ||||||
| chr6:129625082
|
G | T | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4271C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625082 | ||||||
| chr6:129625084
|
TATATGAT others(3): Show |
T | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(5): Show | 8 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4259_786+4268d others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625084 | ||||||
| chr6:129625087
|
AT | A | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4265delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625087 | ||||||
| chr6:129625090
|
A | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+4263T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625090 | ||||||
| chr6:129625091
|
TATATG | T | 20 | a0001c0001t0001g0142a0001c0001t0001g0188a0001c0001t0001g0189others(17): Show | 20 | HG01071.hp1 HG01169.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.786+4257_786+4261d others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625091 | ||||||
| chr6:129625094
|
A | ATAT | 8 | a0001c0001t0003g0219a0001c0001t0003g0222a0001c0001t0008g0118others(5): Show | 8 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4258_786+4259i others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625094 | ||||||
| chr6:129625096
|
G | A | 15 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0108others(12): Show | 15 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.786+4257C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625096 | ||||||
| chr6:129625096
|
G | T | 8 | a0001c0001t0003g0219a0001c0001t0003g0222a0001c0001t0008g0118others(5): Show | 8 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4257C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625096 | ||||||
| chr6:129625097
|
A | T | 15 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0108others(12): Show | 15 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.786+4256T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625097 | ||||||
| chr6:129625098
|
T | A | 11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.786+4255A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625098 | ||||||
| chr6:129625098
|
T | TTATATAT others(1): Show |
2 | a0001c0001t0001g0079a0001c0001t0001g0136 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+4254_786+4255i others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625098 | ||||||
| chr6:129625102
|
TA | T | 20 | a0001c0001t0001g0142a0001c0001t0001g0188a0001c0001t0001g0189others(17): Show | 20 | HG01071.hp1 HG01169.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.786+4250delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625102 | ||||||
| chr6:129625103
|
A | AT | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(5): Show | 8 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4249dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625103 | ||||||
| chr6:129625104
|
T | A | 8 | a0001c0001t0003g0219a0001c0001t0003g0222a0001c0001t0008g0118others(5): Show | 8 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4249A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625104 | ||||||
| chr6:129625105
|
T | G | 4 | a0001c0001t0001g0079a0001c0001t0001g0136a0001c0001t0002g0145others(1): Show | 4 | HG02451.hp1 HG02486.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+4248A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625105 | ||||||
| chr6:129625111
|
TTATATAG others(1): Show |
T | 39 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(36): Show | 40 | HG00621.hp1 HG00639.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.786+4234_786+4241d others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625111 | ||||||
| chr6:129625112
|
T | A | 28 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(25): Show | 28 | HG00099.hp2 HG00735.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.786+4241A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625112 | ||||||
| chr6:129625112
|
T | G | 12 | a0001c0001t0001g0079a0001c0001t0001g0136a0001c0001t0002g0145others(9): Show | 12 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.786+4241A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625112 | ||||||
| chr6:129625117
|
A | AT | 22 | a0001c0001t0001g0079a0001c0001t0001g0129a0001c0001t0001g0136others(19): Show | 22 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.786+4235_786+4236i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625117 | ||||||
| chr6:129625118
|
G | T | 30 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(27): Show | 30 | HG00099.hp2 HG00735.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.786+4235C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625118 | ||||||
| chr6:129625120
|
T | TG | 28 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(25): Show | 28 | HG00099.hp2 HG00735.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.786+4232_786+4233i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625120 | ||||||
| chr6:129625125
|
A | AT | 8 | a0001c0001t0003g0219a0001c0001t0003g0222a0001c0001t0008g0118others(5): Show | 8 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4227dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625125 | ||||||
| chr6:129625125
|
A | G | 10 | a0001c0001t0001g0129a0001c0001t0001g0155a0001c0001t0001g0156others(7): Show | 10 | HG00544.hp2 HG01952.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.786+4228T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625125 | ||||||
| chr6:129625126
|
T | A | 10 | a0001c0001t0001g0129a0001c0001t0001g0155a0001c0001t0001g0156others(7): Show | 10 | HG00544.hp2 HG01952.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.786+4227A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625126 | ||||||
| chr6:129625127
|
T | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0064others(76): Show | 80 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.786+4226A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625127 | ||||||
| chr6:129625133
|
T | TTATATA | 2 | a0001c0001t0001g0079a0001c0001t0001g0136 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+4219_786+4220i others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625133 | ||||||
| chr6:129625133
|
TGA | T | 10 | a0001c0001t0001g0129a0001c0001t0001g0155a0001c0001t0001g0156others(7): Show | 10 | HG00544.hp2 HG01952.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.786+4218_786+4219d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625133 | ||||||
| chr6:129625134
|
G | A | 8 | a0001c0001t0003g0219a0001c0001t0003g0222a0001c0001t0008g0118others(5): Show | 8 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4219C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625134 | ||||||
| chr6:129625134
|
GAT | G | 14 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(11): Show | 14 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.786+4217_786+4218d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625134 | ||||||
| chr6:129625136
|
T | TATATG | 4 | a0001c0001t0002g0145a0001c0001t0007g0077a0001c0001t0010g0137others(1): Show | 4 | HG02451.hp1 HG02896.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+4216_786+4217i others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625136 | ||||||
| chr6:129625138
|
TATATTAT others(25): Show |
T | 1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.786+4183_786+4214d others(34): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625138 | ||||||
| chr6:129625141
|
A | G | 6 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(3): Show | 6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+4212T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625141 | ||||||
| chr6:129625141
|
A | T | 10 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(7): Show | 10 | HG00423.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.786+4212T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625141 | ||||||
| chr6:129625142
|
T | A | 16 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(13): Show | 16 | HG00423.hp1 HG00597.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.786+4211A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625142 | ||||||
| chr6:129625143
|
T | G | 22 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(19): Show | 22 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.786+4210A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625143 | ||||||
| chr6:129625143
|
TATATATT others(6): Show |
T | 1 | a0001c0001t0002g0066 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.786+4197_786+4209d others(15): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625143 | ||||||
| chr6:129625146
|
ATAT | A | 108 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.786+4204_786+4206d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625146 | ||||||
| chr6:129625148
|
A | AT | 6 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(3): Show | 6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+4204dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625148 | ||||||
| chr6:129625149
|
T | TATGATA | 2 | a0001c0001t0007g0077a0003c0004t0005g0088 | 2 | HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.786+4203_786+4204i others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625149 | ||||||
| chr6:129625149
|
TTATATAG others(1): Show |
T | 10 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(7): Show | 10 | HG00423.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.786+4196_786+4203d others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625149 | ||||||
| chr6:129625150
|
T | A | 5 | a0001c0001t0002g0093a0001c0001t0002g0172a0002c0002t0002g0019others(2): Show | 5 | HG00609.hp2 HG01261.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+4203A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625150 | ||||||
| chr6:129625150
|
T | G | 10 | a0001c0001t0001g0079a0001c0001t0001g0136a0001c0001t0003g0219others(7): Show | 10 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.786+4203A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625150 | ||||||
| chr6:129625151
|
A | T | 5 | a0001c0001t0002g0093a0001c0001t0002g0172a0002c0002t0002g0019others(2): Show | 5 | HG00609.hp2 HG01261.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+4202T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625151 | ||||||
| chr6:129625152
|
T | G | 5 | a0001c0001t0002g0093a0001c0001t0002g0172a0002c0002t0002g0019others(2): Show | 5 | HG00609.hp2 HG01261.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+4201A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625152 | ||||||
| chr6:129625152
|
T | TG | 2 | a0001c0001t0007g0077a0003c0004t0005g0088 | 2 | HG02896.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.786+4200_786+4201i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625152 | ||||||
| chr6:129625154
|
T | TG | 6 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(3): Show | 6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+4198_786+4199i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625154 | ||||||
| chr6:129625154
|
TAGA | T | 108 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.786+4196_786+4198d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625154 | ||||||
| chr6:129625155
|
A | AT | 13 | a0001c0001t0001g0079a0001c0001t0001g0107a0001c0001t0001g0136others(10): Show | 13 | HG00408.hp2 HG00558.hp1 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.786+4197_786+4198i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625155 | ||||||
| chr6:129625155
|
A | T | 6 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(3): Show | 6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+4198T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625155 | ||||||
| chr6:129625156
|
G | A | 6 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(3): Show | 6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+4197C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625156 | ||||||
| chr6:129625156
|
G | T | 22 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(19): Show | 22 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.786+4197C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625156 | ||||||
| chr6:129625158
|
T | G | 118 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(115): Show | 118 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.786+4195A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625158 | ||||||
| chr6:129625158
|
T | TATG | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4194_786+4195i others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625158 | ||||||
| chr6:129625158
|
T | TG | 19 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(16): Show | 19 | HG00140.hp2 HG00609.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.786+4194_786+4195i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625158 | ||||||
| chr6:129625163
|
A | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+4190T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625163 | ||||||
| chr6:129625163
|
A | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0136 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+4190T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625163 | ||||||
| chr6:129625164
|
T | A | 4 | a0001c0001t0001g0079a0001c0001t0001g0136a0001c0001t0001g0188others(1): Show | 4 | HG01071.hp1 HG01169.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+4189A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625164 | ||||||
| chr6:129625165
|
T | G | 146 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(143): Show | 146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.786+4188A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625165 | ||||||
| chr6:129625165
|
T | TATATATG | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(5): Show | 8 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4181_786+4187d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625165 | ||||||
| chr6:129625165
|
TATATATG | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0096others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.786+4181_786+4187d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625165 | ||||||
| chr6:129625172
|
G | T | 37 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0084others(34): Show | 37 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(34): Show |
intron_variant | MODIFIER | c.786+4181C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625172 | ||||||
| chr6:129625177
|
A | AG | 8 | a0001c0001t0003g0219a0001c0001t0003g0222a0001c0001t0008g0118others(5): Show | 8 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4175_786+4176i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625177 | ||||||
| chr6:129625178
|
T | A | 8 | a0001c0001t0003g0219a0001c0001t0003g0222a0001c0001t0008g0118others(5): Show | 8 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+4175A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625178 | ||||||
| chr6:129625178
|
T | TATTTA | 5 | a0001c0001t0005g0212a0001c0001t0009g0069a0001c0001t0009g0071others(2): Show | 5 | HG03209.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+4174_786+4175i others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625178 | ||||||
| chr6:129625178
|
T | TATTTATA others(5): Show |
2 | a0001c0001t0005g0207a0001c0001t0007g0077 | 2 | HG00597.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.786+4174_786+4175i others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625178 | ||||||
| chr6:129625179
|
T | G | 26 | a0001c0001t0001g0079a0001c0001t0001g0090a0001c0001t0001g0101others(23): Show | 26 | HG00741.hp2 HG01192.hp2 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.786+4174A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625179 | ||||||
| chr6:129625182
|
A | G | 5 | a0001c0001t0005g0212a0001c0001t0009g0069a0001c0001t0009g0071others(2): Show | 5 | HG03209.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+4171T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625182 | ||||||
| chr6:129625182
|
ATAT | A | 3 | a0001c0001t0001g0216a0001c0001t0001g0218a0002c0002t0001g0038 | 3 | NA18943.hp2 NA18963.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.786+4168_786+4170d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625182 | ||||||
| chr6:129625185
|
T | A | 5 | a0001c0001t0005g0212a0001c0001t0009g0069a0001c0001t0009g0071others(2): Show | 5 | HG03209.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+4168A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625185 | ||||||
| chr6:129625186
|
T | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0090others(53): Show | 57 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.786+4167A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625186 | ||||||
| chr6:129625186
|
T | TATATATG others(66): Show |
1 | a0001c0001t0007g0078 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.786+4166_786+4167i others(75): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625186 | ||||||
| chr6:129625186
|
TATATATG others(17): Show |
T | 13 | a0001c0001t0001g0142a0001c0001t0002g0125a0001c0001t0002g0223others(10): Show | 13 | HG01192.hp2 HG02257.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.786+4143_786+4166d others(26): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625186 | ||||||
| chr6:129625191
|
A | G | 1 | a0002c0002t0001g0017 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.786+4162T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625191 | ||||||
| chr6:129625191
|
AT | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+4161delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625191 | ||||||
| chr6:129625193
|
G | A | 5 | a0001c0001t0001g0090a0001c0001t0001g0101a0001c0001t0001g0155others(2): Show | 5 | HG00741.hp2 HG01361.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+4160C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625193 | ||||||
| chr6:129625194
|
A | T | 5 | a0001c0001t0001g0090a0001c0001t0001g0101a0001c0001t0001g0155others(2): Show | 5 | HG00741.hp2 HG01361.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+4159T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625194 | ||||||
| chr6:129625194
|
ATATATAT others(1): Show |
A | 3 | a0001c0001t0003g0219a0002c0002t0003g0022a0002c0002t0003g0023 | 3 | HG00558.hp1 HG02129.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.786+4151_786+4158d others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625194 | ||||||
| chr6:129625195
|
T | G | 1 | a0002c0002t0003g0043 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.786+4158A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625195 | ||||||
| chr6:129625198
|
ATAT | A | 3 | a0001c0001t0008g0118a0001c0001t0008g0228a0002c0002t0014g0045 | 3 | HG02922.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.786+4152_786+4154d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625198 | ||||||
| chr6:129625198
|
ATATTTAT others(3): Show |
A | 2 | a0001c0001t0003g0222a0002c0002t0003g0037 | 2 | HG00408.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.786+4145_786+4154d others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625198 | ||||||
| chr6:129625199
|
T | TG | 5 | a0001c0001t0005g0212a0001c0001t0009g0069a0001c0001t0009g0071others(2): Show | 5 | HG03209.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+4153_786+4154i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625199 | ||||||
| chr6:129625199
|
TA | T | 3 | a0001c0001t0001g0216a0001c0001t0001g0218a0002c0002t0001g0038 | 3 | NA18943.hp2 NA18963.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.786+4153delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625199 | ||||||
| chr6:129625201
|
T | G | 3 | a0001c0001t0001g0216a0001c0001t0001g0218a0002c0002t0001g0038 | 3 | NA18943.hp2 NA18963.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.786+4152A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625201 | ||||||
| chr6:129625201
|
TTTATATG others(3): Show |
T | 47 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0096others(44): Show | 48 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.786+4142_786+4151d others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625201 | ||||||
| chr6:129625202
|
T | A | 9 | a0001c0001t0001g0216a0001c0001t0001g0218a0001c0001t0005g0212others(6): Show | 9 | HG02451.hp2 HG03209.hp2 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.786+4151A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625202 | ||||||
| chr6:129625202
|
T | TA | 4 | a0001c0001t0001g0090a0001c0001t0001g0101a0001c0001t0001g0155others(1): Show | 4 | HG00741.hp2 HG01361.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+4150_786+4151i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625202 | ||||||
| chr6:129625203
|
T | G | 3 | a0001c0001t0008g0118a0001c0001t0008g0228a0002c0002t0014g0045 | 3 | HG02922.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.786+4150A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625203 | ||||||
| chr6:129625207
|
TG | T | 5 | a0001c0001t0005g0212a0001c0001t0009g0069a0001c0001t0009g0071others(2): Show | 5 | HG03209.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+4145delC | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625207 | ||||||
| chr6:129625208
|
G | A | 4 | a0001c0001t0008g0118a0001c0001t0008g0228a0002c0002t0014g0045others(1): Show | 4 | HG02922.hp2 HG03098.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+4145C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625208 | ||||||
| chr6:129625208
|
G | GATA | 3 | a0001c0001t0001g0090a0001c0001t0001g0101a0001c0001t0001g0232 | 3 | HG00741.hp2 HG01361.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.786+4144_786+4145i others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625208 | ||||||
| chr6:129625208
|
GTAAT | G | 5 | a0001c0001t0001g0155a0001c0001t0001g0216a0001c0001t0001g0218others(2): Show | 5 | HG02451.hp2 NA18943.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+4141_786+4144d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625208 | ||||||
| chr6:129625209
|
T | A | 3 | a0001c0001t0003g0219a0002c0002t0003g0022a0002c0002t0003g0023 | 3 | HG00558.hp1 HG02129.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.786+4144A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625209 | ||||||
| chr6:129625210
|
A | G | 2 | a0001c0001t0003g0222a0002c0002t0003g0037 | 2 | HG00408.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.786+4143T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625210 | ||||||
| chr6:129625210
|
A | T | 12 | a0001c0001t0003g0219a0001c0001t0005g0212a0001c0001t0008g0118others(9): Show | 12 | HG00558.hp1 HG02129.hp1 HG02155.hp1 others(9): Show |
intron_variant | MODIFIER | c.786+4143T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625210 | ||||||
| chr6:129625211
|
A | T | 4 | a0001c0001t0001g0090a0001c0001t0001g0101a0001c0001t0001g0232others(1): Show | 4 | HG00597.hp2 HG00741.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+4142T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625211 | ||||||
| chr6:129625212
|
T | G | 3 | a0001c0001t0001g0090a0001c0001t0001g0101a0001c0001t0001g0232 | 3 | HG00741.hp2 HG01361.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.786+4141A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625212 | ||||||
| chr6:129625215
|
A | G | 5 | a0001c0001t0005g0212a0001c0001t0009g0069a0001c0001t0009g0071others(2): Show | 5 | HG03209.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+4138T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625215 | ||||||
| chr6:129625219
|
G | GATATATG others(19): Show |
1 | a0001c0001t0001g0136 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.786+4133_786+4134i others(28): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625219 | ||||||
| chr6:129625219
|
G | GATATATG others(52): Show |
1 | a0001c0001t0005g0207 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.786+4133_786+4134i others(61): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625219 | ||||||
| chr6:129625219
|
G | GATATATG others(26): Show |
3 | a0001c0001t0001g0164a0001c0001t0002g0184a0001c0001t0003g0183 | 3 | NA18969.hp2 NA18990.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.786+4101_786+4133d others(35): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625219 | ||||||
| chr6:129625219
|
G | GATATATG others(59): Show |
1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.786+4068_786+4133d others(68): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625219 | ||||||
| chr6:129625219
|
G | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(53): Show | 57 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.786+4134C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625219 | ||||||
| chr6:129625219
|
GATATATG others(26): Show |
G | 2 | a0001c0001t0001g0065a0001c0001t0002g0068 | 2 | HG00438.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.786+4101_786+4133d others(35): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625219 | ||||||
| chr6:129625219
|
GATATATG others(59): Show |
G | 2 | a0001c0001t0002g0093a0002c0002t0002g0019 | 2 | HG00609.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.786+4068_786+4133d others(68): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625219 | ||||||
| chr6:129625226
|
G | T | 5 | a0001c0001t0001g0090a0001c0001t0001g0101a0001c0001t0001g0155others(2): Show | 5 | HG00741.hp2 HG01361.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+4127C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625226 | ||||||
| chr6:129625233
|
G | T | 1 | a0001c0001t0001g0155 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.786+4120C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625233 | ||||||
| chr6:129625233
|
GATATATA others(10): Show |
G | 1 | a0002c0002t0003g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.786+4103_786+4119d others(19): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625233 | ||||||
| chr6:129625239
|
TATTTATA others(5): Show |
T | 65 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0096others(62): Show | 66 | HG00408.hp2 HG00544.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.786+4102_786+4113d others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625239 | ||||||
| chr6:129625241
|
TTTA | T | 5 | a0001c0001t0001g0090a0001c0001t0001g0101a0001c0001t0001g0188others(2): Show | 5 | HG00741.hp2 HG01071.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+4109_786+4111d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625241 | ||||||
| chr6:129625242
|
T | A | 1 | a0001c0001t0001g0155 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.786+4111A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625242 | ||||||
| chr6:129625248
|
G | A | 3 | a0001c0001t0001g0155a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG01071.hp1 HG01169.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.786+4105C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625248 | ||||||
| chr6:129625251
|
A | T | 6 | a0001c0001t0001g0090a0001c0001t0001g0101a0001c0001t0001g0155others(3): Show | 6 | HG00741.hp2 HG01071.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+4102T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625251 | ||||||
| chr6:129625252
|
T | TATATATG | 12 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.786+4094_786+4100d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625252 | ||||||
| chr6:129625259
|
G | T | 45 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0096others(42): Show | 46 | HG00544.hp2 HG00621.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.786+4094C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625259 | ||||||
| chr6:129625268
|
T | TATATGAT others(36): Show |
1 | a0001c0001t0007g0077 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.786+4084_786+4085i others(45): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625268 | ||||||
| chr6:129625272
|
TATTTATA others(5): Show |
T | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+4069_786+4080d others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625272 | ||||||
| chr6:129625274
|
TTTA | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0096others(43): Show | 47 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.786+4076_786+4078d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625274 | ||||||
| chr6:129625284
|
A | T | 46 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0096others(43): Show | 47 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.786+4069T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625284 | ||||||
| chr6:129625285
|
TATATATG | T | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4061_786+4067d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625285 | ||||||
| chr6:129625292
|
G | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+4061C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625292 | ||||||
| chr6:129625292
|
GATATATG others(19): Show |
G | 3 | a0001c0001t0001g0090a0001c0001t0001g0101a0001c0001t0001g0232 | 3 | HG00741.hp2 HG01361.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.786+4035_786+4060d others(28): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625292 | ||||||
| chr6:129625299
|
G | T | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4054C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625299 | ||||||
| chr6:129625311
|
TATGTA | T | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4037_786+4041d others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625311 | ||||||
| chr6:129625316
|
AAT | A | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.786+4035_786+4036d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625316 | ||||||
| chr6:129625317
|
A | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+4036T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625317 | ||||||
| chr6:129625318
|
T | TATATATG | 46 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0096others(43): Show | 47 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.786+4028_786+4034d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625318 | ||||||
| chr6:129625325
|
G | T | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4028C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625325 | ||||||
| chr6:129625327
|
TATATG | T | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4021_786+4025d others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625327 | ||||||
| chr6:129625331
|
TG | T | 4 | a0001c0001t0001g0216a0001c0001t0001g0218a0002c0002t0001g0038others(1): Show | 4 | HG02451.hp2 NA18943.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+4021delC | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625331 | ||||||
| chr6:129625335
|
A | T | 4 | a0001c0001t0001g0216a0001c0001t0001g0218a0002c0002t0001g0038others(1): Show | 4 | HG02451.hp2 NA18943.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+4018T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625335 | ||||||
| chr6:129625337
|
A | T | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4016T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625337 | ||||||
| chr6:129625337
|
ATATTTAT others(136): Show |
A | 4 | a0001c0001t0001g0216a0001c0001t0001g0218a0002c0002t0001g0038others(1): Show | 4 | HG02451.hp2 NA18943.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+3873_786+4015d others(2): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625337 | ||||||
| chr6:129625341
|
T | A | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4012A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625341 | ||||||
| chr6:129625342
|
T | C | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4011A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625342 | ||||||
| chr6:129625350
|
A | T | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+4003T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625350 | ||||||
| chr6:129625356
|
ATT | A | 10 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(7): Show | 10 | HG00423.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.786+3995_786+3996d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625356 | ||||||
| chr6:129625357
|
T | TGATA | 3 | a0001c0001t0005g0212a0001c0001t0009g0069a0002c0002t0005g0024 | 3 | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.786+3995_786+3996i others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625357 | ||||||
| chr6:129625357
|
TTATGTAT others(5): Show |
T | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3984_786+3995d others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625357 | ||||||
| chr6:129625358
|
T | G | 24 | a0001c0001t0001g0136a0001c0001t0001g0142a0001c0001t0002g0125others(21): Show | 24 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.786+3995A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625358 | ||||||
| chr6:129625359
|
A | ATATATGA others(83): Show |
1 | a0001c0001t0001g0136 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.786+3993_786+3994i others(92): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625359 | ||||||
| chr6:129625361
|
G | A | 225 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(222): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.786+3992C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625361 | ||||||
| chr6:129625361
|
G | GATA | 3 | a0001c0001t0005g0212a0001c0001t0009g0069a0002c0002t0005g0024 | 3 | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.786+3991_786+3992i others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625361 | ||||||
| chr6:129625364
|
TATTTA | T | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3984_786+3988d others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625364 | ||||||
| chr6:129625367
|
T | A | 1 | a0001c0001t0009g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.786+3986A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625367 | ||||||
| chr6:129625369
|
A | ATATATAT | 48 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(45): Show | 49 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.786+3977_786+3983d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625369 | ||||||
| chr6:129625369
|
ATATATAT others(104): Show |
A | 21 | a0001c0001t0001g0142a0001c0001t0002g0125a0001c0001t0002g0223others(18): Show | 21 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.786+3873_786+3983d others(2): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625369 | ||||||
| chr6:129625370
|
T | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3983A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625370 | ||||||
| chr6:129625373
|
A | G | 3 | a0001c0001t0005g0212a0001c0001t0009g0069a0002c0002t0005g0024 | 3 | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.786+3980T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625373 | ||||||
| chr6:129625373
|
A | T | 1 | a0001c0001t0009g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.786+3980T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625373 | ||||||
| chr6:129625375
|
A | T | 1 | a0003c0004t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.786+3978T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625375 | ||||||
| chr6:129625376
|
T | A | 3 | a0001c0001t0005g0212a0001c0001t0009g0069a0002c0002t0005g0024 | 3 | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.786+3977A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625376 | ||||||
| chr6:129625377
|
T | G | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3976A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625377 | ||||||
| chr6:129625380
|
A | G | 1 | a0001c0001t0009g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.786+3973T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625380 | ||||||
| chr6:129625383
|
T | A | 1 | a0001c0001t0009g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.786+3970A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625383 | ||||||
| chr6:129625384
|
T | G | 5 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0005g0212others(2): Show | 5 | HG01071.hp1 HG01169.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3969A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625384 | ||||||
| chr6:129625385
|
A | T | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3968T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625385 | ||||||
| chr6:129625386
|
T | TATATG | 3 | a0001c0001t0005g0212a0001c0001t0009g0069a0002c0002t0005g0024 | 3 | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.786+3966_786+3967i others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625386 | ||||||
| chr6:129625391
|
T | A | 3 | a0001c0001t0005g0212a0001c0001t0009g0069a0002c0002t0005g0024 | 3 | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.786+3962A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625391 | ||||||
| chr6:129625391
|
T | TA | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3961_786+3962i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625391 | ||||||
| chr6:129625395
|
A | T | 5 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0005g0212others(2): Show | 5 | HG01071.hp1 HG01169.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3958T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625395 | ||||||
| chr6:129625395
|
AC | A | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3957delG | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625395 | ||||||
| chr6:129625396
|
C | T | 7 | a0001c0001t0001g0079a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG01071.hp1 HG01169.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.786+3957G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625396 | ||||||
| chr6:129625397
|
A | T | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3956T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625397 | ||||||
| chr6:129625401
|
G | A | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3952C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625401 | ||||||
| chr6:129625401
|
G | T | 1 | a0001c0001t0009g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.786+3952C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625401 | ||||||
| chr6:129625404
|
T | A | 5 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0005g0212others(2): Show | 5 | HG01071.hp1 HG01169.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3949A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625404 | ||||||
| chr6:129625408
|
A | G | 11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.786+3945T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625408 | ||||||
| chr6:129625413
|
A | T | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3940T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625413 | ||||||
| chr6:129625415
|
A | ATATTATA others(14): Show |
1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.786+3937_786+3938i others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625415 | ||||||
| chr6:129625415
|
A | ATATTATA others(152): Show |
1 | a0003c0004t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.786+3937_786+3938i others(161): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625415 | ||||||
| chr6:129625417
|
A | G | 1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.786+3936T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625417 | ||||||
| chr6:129625418
|
TAA | T | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3933_786+3934d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625418 | ||||||
| chr6:129625419
|
A | ATTT | 3 | a0001c0001t0005g0212a0001c0001t0009g0069a0002c0002t0005g0024 | 3 | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.786+3933_786+3934i others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625419 | ||||||
| chr6:129625419
|
A | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(46): Show | 50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.786+3934T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625419 | ||||||
| chr6:129625419
|
A | T | 2 | a0001c0001t0009g0071a0003c0004t0005g0088 | 2 | NA18612.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.786+3934T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625419 | ||||||
| chr6:129625419
|
AATATAT | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3928_786+3933d others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625419 | ||||||
| chr6:129625420
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0015g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.786+3932_786+3933i others(30): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625420 | ||||||
| chr6:129625420
|
A | ATATATAT others(23): Show |
12 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(9): Show | 12 | HG00423.hp1 HG02155.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.786+3903_786+3932d others(32): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625420 | ||||||
| chr6:129625420
|
A | ATATATAT others(53): Show |
4 | a0001c0001t0001g0140a0001c0001t0001g0221a0001c0001t0003g0138others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+3873_786+3932d others(62): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625420 | ||||||
| chr6:129625420
|
A | ATATATAT others(67): Show |
1 | a0001c0001t0001g0136 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.786+3932_786+3933i others(76): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625420 | ||||||
| chr6:129625420
|
A | G | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.786+3933T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625420 | ||||||
| chr6:129625420
|
A | T | 3 | a0001c0001t0001g0079a0001c0011t0001g0056a0003c0004t0001g0151 | 3 | HG03098.hp2 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.786+3933T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625420 | ||||||
| chr6:129625420
|
ATATATAT others(23): Show |
A | 5 | a0001c0001t0001g0061a0001c0001t0001g0064a0001c0001t0001g0111others(2): Show | 5 | HG00140.hp1 HG01433.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3903_786+3932d others(32): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625420 | ||||||
| chr6:129625426
|
A | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3927T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625426 | ||||||
| chr6:129625427
|
T | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(47): Show | 51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+3926A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625427 | ||||||
| chr6:129625429
|
A | ATAAATTT others(116): Show |
1 | a0003c0004t0005g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.786+3923_786+3924i others(125): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625429 | ||||||
| chr6:129625434
|
TAATATAT others(57): Show |
T | 49 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(46): Show | 50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.786+3855_786+3918d others(66): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625434 | ||||||
| chr6:129625435
|
A | C | 1 | a0001c0001t0009g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.786+3918T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625435 | ||||||
| chr6:129625435
|
A | T | 3 | a0001c0001t0005g0212a0001c0001t0009g0069a0002c0002t0005g0024 | 3 | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.786+3918T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625435 | ||||||
| chr6:129625436
|
A | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3917T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625436 | ||||||
| chr6:129625440
|
A | ATTTATAC others(5): Show |
3 | a0001c0001t0005g0212a0001c0001t0009g0069a0002c0002t0005g0024 | 3 | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.786+3912_786+3913i others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625440 | ||||||
| chr6:129625440
|
A | G | 1 | a0001c0001t0009g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.786+3913T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625440 | ||||||
| chr6:129625445
|
T | A | 6 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0005g0212others(3): Show | 6 | HG01071.hp1 HG01169.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+3908A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625445 | ||||||
| chr6:129625451
|
T | A | 2 | a0001c0001t0005g0207a0001c0011t0001g0056 | 2 | HG00597.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.786+3902A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625451 | ||||||
| chr6:129625458
|
TA | T | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3894delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625458 | ||||||
| chr6:129625463
|
AT | A | 3 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0002g0113 | 3 | HG01071.hp1 HG01169.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.786+3889delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625463 | ||||||
| chr6:129625465
|
A | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3888T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625465 | ||||||
| chr6:129625465
|
A | T | 2 | a0001c0001t0001g0136a0002c0002t0001g0040 | 2 | HG02486.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.786+3888T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625465 | ||||||
| chr6:129625470
|
A | G | 3 | a0001c0001t0001g0111a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG01071.hp1 HG01169.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.786+3883T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625470 | ||||||
| chr6:129625472
|
A | T | 1 | a0001c0001t0002g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.786+3881T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625472 | ||||||
| chr6:129625473
|
T | TTTTATAT others(21): Show |
1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.786+3879_786+3880i others(30): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625473 | ||||||
| chr6:129625475
|
T | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3878A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625475 | ||||||
| chr6:129625479
|
A | ATAATATA others(127): Show |
11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.786+3873_786+3874i others(136): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625479 | ||||||
| chr6:129625488
|
T | A | 1 | a0003c0004t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.786+3865A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625488 | ||||||
| chr6:129625488
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.786+3865A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625488 | ||||||
| chr6:129625500
|
A | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(46): Show | 50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.786+3853T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625500 | ||||||
| chr6:129625504
|
T | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(47): Show | 51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+3849A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625504 | ||||||
| chr6:129625509
|
A | ATTATATA others(199): Show |
2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.786+3843_786+3844i others(208): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625509 | ||||||
| chr6:129625513
|
C | A | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.786+3840G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625513 | ||||||
| chr6:129625514
|
A | T | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.786+3839T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625514 | ||||||
| chr6:129625527
|
C | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.786+3826G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625527 | ||||||
| chr6:129625542
|
T | C | 51 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.786+3811A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625542 | ||||||
| chr6:129625551
|
T | TTATA | 51 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.786+3801_786+3802i others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625551 | ||||||
| chr6:129625569
|
C | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.786+3784G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625569 | ||||||
| chr6:129625585
|
T | G | 1 | a0001c0001t0001g0202 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.786+3768A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625585 | ||||||
| chr6:129625594
|
T | G | 1 | a0001c0001t0003g0224 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.786+3759A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625594 | ||||||
| chr6:129625606
|
A | C | 12 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(9): Show | 12 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.786+3747T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625606 | ||||||
| chr6:129625607
|
T | TTATTATA others(23): Show |
11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.786+3716_786+3745d others(32): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625607 | ||||||
| chr6:129625607
|
TTATTATA others(8): Show |
T | 1 | a0001c0001t0001g0213 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.786+3731_786+3745d others(17): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625607 | ||||||
| chr6:129625616
|
AT | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.786+3736delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625616 | ||||||
| chr6:129625633
|
AT | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(47): Show | 51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+3719delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625633 | ||||||
| chr6:129625637
|
A | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.786+3716T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625637 | ||||||
| chr6:129625639
|
A | G | 9 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(6): Show | 9 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.786+3714T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625639 | ||||||
| chr6:129625658
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0136 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+3695A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625658 | ||||||
| chr6:129625670
|
TTATATTA others(25): Show |
T | 1 | a0001c0001t0001g0178 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.786+3651_786+3682d others(34): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625670 | ||||||
| chr6:129625675
|
TTA | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(47): Show | 51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+3676_786+3677d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625675 | ||||||
| chr6:129625677
|
A | ATATATAT others(51): Show |
1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.786+3618_786+3675d others(60): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625677 | ||||||
| chr6:129625681
|
A | T | 1 | a0001c0001t0002g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.786+3672T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625681 | ||||||
| chr6:129625693
|
T | C | 1 | a0001c0001t0001g0210 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.786+3660A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625693 | ||||||
| chr6:129625700
|
T | A | 50 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(47): Show | 51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+3653A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625700 | ||||||
| chr6:129625702
|
A | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(47): Show | 51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+3651T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625702 | ||||||
| chr6:129625704
|
A | C | 50 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(47): Show | 51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+3649T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625704 | ||||||
| chr6:129625728
|
A | ATATTAAT others(29): Show |
2 | a0001c0001t0001g0079a0001c0001t0001g0136 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+3624_786+3625i others(38): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625728 | ||||||
| chr6:129625728
|
A | ATATTAAT others(61): Show |
2 | a0003c0004t0001g0151a0003c0004t0005g0088 | 2 | HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.786+3624_786+3625i others(70): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625728 | ||||||
| chr6:129625729
|
TATTTA | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(47): Show | 51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+3619_786+3623d others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625729 | ||||||
| chr6:129625732
|
T | TAATA | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3620_786+3621i others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625732 | ||||||
| chr6:129625732
|
T | TTATA | 6 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(3): Show | 6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+3620_786+3621i others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625732 | ||||||
| chr6:129625732
|
TTATTATA others(8): Show |
T | 3 | a0001c0001t0001g0083a0001c0001t0001g0215a0001c0001t0003g0237 | 3 | HG02074.hp2 HG02257.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.786+3606_786+3620d others(17): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625732 | ||||||
| chr6:129625739
|
ATATT | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(46): Show | 50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.786+3610_786+3613d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625739 | ||||||
| chr6:129625746
|
T | A | 1 | a0002c0002t0001g0052 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.786+3607A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625746 | ||||||
| chr6:129625750
|
T | A | 49 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(46): Show | 50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.786+3603A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625750 | ||||||
| chr6:129625750
|
T | TTA | 7 | a0001c0001t0002g0145a0001c0001t0005g0207a0001c0001t0005g0212others(4): Show | 7 | HG00597.hp2 HG02451.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.786+3601_786+3602d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625750 | ||||||
| chr6:129625760
|
A | T | 50 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(47): Show | 51 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.786+3593T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625760 | ||||||
| chr6:129625762
|
A | T | 7 | a0001c0001t0002g0145a0001c0001t0005g0207a0001c0001t0005g0212others(4): Show | 7 | HG00597.hp2 HG02451.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.786+3591T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625762 | ||||||
| chr6:129625766
|
T | A | 1 | a0001c0001t0001g0178 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.786+3587A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625766 | ||||||
| chr6:129625771
|
A | T | 49 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(46): Show | 50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.786+3582T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625771 | ||||||
| chr6:129625772
|
TATTTATA others(7): Show |
T | 49 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(46): Show | 50 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.786+3567_786+3580d others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625772 | ||||||
| chr6:129625773
|
A | T | 5 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(2): Show | 5 | HG00597.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3580T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625773 | ||||||
| chr6:129625775
|
T | A | 8 | a0001c0001t0002g0145a0001c0001t0005g0207a0001c0001t0005g0212others(5): Show | 8 | HG00597.hp2 HG02451.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.786+3578A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625775 | ||||||
| chr6:129625777
|
A | T | 1 | a0001c0001t0001g0178 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.786+3576T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625777 | ||||||
| chr6:129625778
|
TATATATA | T | 27 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0074others(24): Show | 27 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(24): Show |
intron_variant | MODIFIER | c.786+3568_786+3574d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625778 | ||||||
| chr6:129625779
|
A | AT | 5 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(2): Show | 5 | HG00597.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3573dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625779 | ||||||
| chr6:129625779
|
A | ATATATAT others(8): Show |
1 | a0001c0003t0002g0175 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.786+3573_786+3574i others(17): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625779 | ||||||
| chr6:129625779
|
A | T | 3 | a0001c0001t0002g0145a0001c0001t0010g0137a0001c0011t0001g0056 | 3 | HG02451.hp1 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.786+3574T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625779 | ||||||
| chr6:129625781
|
ATATAATA others(6): Show |
A | 1 | a0001c0001t0001g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.786+3559_786+3571d others(15): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625781 | ||||||
| chr6:129625785
|
A | AT | 6 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(3): Show | 6 | HG00597.hp2 HG00733.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+3567_786+3568i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625785 | ||||||
| chr6:129625785
|
A | T | 1 | a0001c0001t0001g0178 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.786+3568T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625785 | ||||||
| chr6:129625786
|
A | T | 11 | a0001c0001t0001g0146a0001c0001t0001g0178a0001c0001t0002g0145others(8): Show | 11 | HG00597.hp2 HG00733.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.786+3567T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625786 | ||||||
| chr6:129625792
|
A | T | 1 | a0002c0002t0001g0049 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.786+3561T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625792 | ||||||
| chr6:129625794
|
T | A | 3 | a0001c0001t0002g0145a0001c0001t0010g0137a0001c0011t0001g0056 | 3 | HG02451.hp1 HG03195.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.786+3559A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625794 | ||||||
| chr6:129625794
|
T | TA | 5 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(2): Show | 5 | HG00597.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3558_786+3559i others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625794 | ||||||
| chr6:129625796
|
T | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(53): Show | 57 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.786+3557A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625796 | ||||||
| chr6:129625800
|
AT | A | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+3552delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625800 | ||||||
| chr6:129625801
|
T | G | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.786+3552A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625801 | ||||||
| chr6:129625801
|
T | TTTA | 5 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(2): Show | 5 | HG00597.hp2 NA18612.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3551_786+3552i others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625801 | ||||||
| chr6:129625802
|
T | A | 1 | a0001c0001t0001g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.786+3551A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625802 | ||||||
| chr6:129625803
|
A | T | 1 | a0001c0001t0001g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.786+3550T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625803 | ||||||
| chr6:129625804
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.786+3549A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625804 | ||||||
| chr6:129625808
|
T | A | 8 | a0001c0001t0002g0145a0001c0001t0005g0207a0001c0001t0005g0212others(5): Show | 8 | HG00597.hp2 HG02451.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.786+3545A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625808 | ||||||
| chr6:129625813
|
T | C | 3 | a0001c0003t0002g0175a0003c0004t0001g0151a0003c0004t0005g0088 | 3 | HG03098.hp2 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.786+3540A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625813 | ||||||
| chr6:129625818
|
A | T | 8 | a0001c0001t0002g0145a0001c0001t0005g0207a0001c0001t0005g0212others(5): Show | 8 | HG00597.hp2 HG02451.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.786+3535T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625818 | ||||||
| chr6:129625820
|
A | G | 25 | a0001c0001t0001g0142a0001c0001t0001g0216a0001c0001t0001g0218others(22): Show | 25 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.786+3533T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625820 | ||||||
| chr6:129625835
|
C | T | 19 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(16): Show | 19 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.786+3518G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625835 | ||||||
| chr6:129625849
|
ATAT | A | 3 | a0001c0001t0002g0171a0001c0001t0002g0217a0002c0002t0001g0026 | 3 | HG02056.hp2 HG02523.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.786+3501_786+3503d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625849 | ||||||
| chr6:129625852
|
T | TTATACAT others(37): Show |
2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.786+3500_786+3501i others(46): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625852 | ||||||
| chr6:129625853
|
T | TATATTTA others(54): Show |
8 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(5): Show | 8 | HG00423.hp1 HG02717.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+3499_786+3500i others(63): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625853 | ||||||
| chr6:129625855
|
T | TAC | 19 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(16): Show | 19 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.786+3497_786+3498i others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625855 | ||||||
| chr6:129625857
|
TTTATATA | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.786+3489_786+3495d others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625857 | ||||||
| chr6:129625867
|
A | ATATATTA others(59): Show |
1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.786+3420_786+3485d others(68): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625867 | ||||||
| chr6:129625872
|
TTA | T | 19 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(16): Show | 19 | HG00140.hp2 HG00597.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.786+3479_786+3480d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625872 | ||||||
| chr6:129625876
|
A | T | 1 | a0001c0001t0002g0125 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.786+3477T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625876 | ||||||
| chr6:129625894
|
T | TTTATATA others(78): Show |
2 | a0001c0001t0003g0138a0001c0001t0011g0141 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.786+3458_786+3459i others(87): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625894 | ||||||
| chr6:129625897
|
T | G | 2 | a0001c0001t0003g0138a0001c0001t0011g0141 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.786+3456A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625897 | ||||||
| chr6:129625902
|
TTA | T | 51 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.786+3449_786+3450d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625902 | ||||||
| chr6:129625904
|
A | T | 1 | a0001c0001t0001g0067 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.786+3449T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625904 | ||||||
| chr6:129625908
|
A | ATTATATA others(8): Show |
11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.786+3444_786+3445i others(17): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625908 | ||||||
| chr6:129625919
|
TAG | T | 3 | a0001c0001t0001g0079a0001c0001t0003g0138a0001c0001t0011g0141 | 3 | HG02615.hp1 HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.786+3432_786+3433d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625919 | ||||||
| chr6:129625921
|
G | T | 62 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(59): Show | 63 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.786+3432C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625921 | ||||||
| chr6:129625932
|
A | G | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.786+3421T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625932 | ||||||
| chr6:129625935
|
ATATAT | A | 4 | a0001c0001t0002g0145a0001c0001t0010g0137a0003c0004t0001g0151others(1): Show | 4 | HG02451.hp1 HG03098.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+3413_786+3417d others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625935 | ||||||
| chr6:129625942
|
ATATATTT others(6): Show |
A | 51 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.786+3398_786+3410d others(15): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625942 | ||||||
| chr6:129625957
|
ATATATT | A | 13 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(10): Show | 13 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.786+3390_786+3395d others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625957 | ||||||
| chr6:129625970
|
TTA | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0136 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+3381_786+3382d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129625970 | ||||||
| chr6:129626039
|
T | TAC | 2 | a0001c0001t0001g0073a0001c0001t0001g0201 | 2 | HG01081.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.786+3312_786+3313d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626039 | ||||||
| chr6:129626041
|
C | T | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.786+3312G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626041 | ||||||
| chr6:129626065
|
T | C | 3 | a0001c0001t0001g0203a0003c0004t0001g0151a0003c0004t0005g0088 | 3 | HG01517.hp1 HG03098.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.786+3288A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | ||||||
| chr6:129626065
|
T | TAC | 32 | a0001c0001t0001g0065a0001c0001t0001g0109a0001c0001t0001g0126others(29): Show | 32 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.786+3286_786+3287d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | ||||||
| chr6:129626065
|
T | TACAC | 29 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0072others(26): Show | 29 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.786+3284_786+3287d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | ||||||
| chr6:129626065
|
T | TACACAC | 51 | a0001c0001t0001g0074a0001c0001t0001g0086a0001c0001t0001g0089others(48): Show | 51 | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.786+3282_786+3287d others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | ||||||
| chr6:129626065
|
T | TACACACA others(1): Show |
14 | a0001c0001t0001g0064a0001c0001t0001g0067a0001c0001t0001g0083others(11): Show | 14 | HG00099.hp2 HG00423.hp1 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.786+3280_786+3287d others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | ||||||
| chr6:129626065
|
T | TACACACA others(3): Show |
8 | a0001c0001t0001g0063a0001c0001t0001g0130a0001c0001t0001g0148others(5): Show | 8 | HG00423.hp2 HG01928.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.786+3278_786+3287d others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | ||||||
| chr6:129626065
|
T | TACACACA others(5): Show |
3 | a0001c0001t0001g0091a0001c0001t0001g0210a0001c0001t0011g0141 | 3 | HG02615.hp1 HG02976.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.786+3276_786+3287d others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | ||||||
| chr6:129626065
|
T | TACACACA others(7): Show |
1 | a0001c0001t0006g0060 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.786+3274_786+3287d others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | ||||||
| chr6:129626065
|
T | TACACACA others(9): Show |
1 | a0002c0002t0001g0054 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.786+3272_786+3287d others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | ||||||
| chr6:129626065
|
TAC | T | 9 | a0001c0001t0001g0216a0001c0001t0003g0219a0001c0001t0003g0222others(6): Show | 9 | HG00408.hp2 HG00558.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.786+3286_786+3287d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | ||||||
| chr6:129626065
|
TACAC | T | 16 | a0001c0001t0001g0142a0001c0001t0001g0218a0001c0001t0002g0125others(13): Show | 16 | HG01192.hp2 HG02451.hp2 HG02895.hp1 others(13): Show |
intron_variant | MODIFIER | c.786+3284_786+3287d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | ||||||
| chr6:129626065
|
TACACACA others(1): Show |
T | 1 | a0001c0001t0001g0001 | 2 | HG00738.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.786+3280_786+3287d others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | ||||||
| chr6:129626065
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0004g0123 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.786+3278_786+3287d others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | ||||||
| chr6:129626065
|
TACACACA others(5): Show |
T | 1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.786+3276_786+3287d others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | ||||||
| chr6:129626065
|
TACACACA others(17): Show |
T | 1 | a0001c0001t0002g0182 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.786+3264_786+3287d others(26): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626065 | ||||||
| chr6:129626073
|
C | CACACACA others(7): Show |
1 | a0003c0004t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.786+3279_786+3280i others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626073 | ||||||
| chr6:129626075
|
C | CACACACA others(9): Show |
1 | a0003c0004t0005g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.786+3277_786+3278i others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626075 | ||||||
| chr6:129626101
|
CACACAT | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0136 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+3246_786+3251d others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626101 | ||||||
| chr6:129626103
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG00738.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.786+3250G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626103 | ||||||
| chr6:129626105
|
C | CACACACA others(9): Show |
4 | a0001c0001t0001g0096a0001c0001t0001g0131a0001c0001t0002g0162others(1): Show | 4 | HG01081.hp2 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+3247_786+3248i others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626105 | ||||||
| chr6:129626105
|
C | CACACACA others(7): Show |
8 | a0001c0001t0001g0102a0001c0001t0001g0129a0001c0001t0001g0155others(5): Show | 8 | HG00738.hp1 HG03516.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.786+3247_786+3248i others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626105 | ||||||
| chr6:129626105
|
C | CACACACA others(3): Show |
1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.786+3247_786+3248i others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626105 | ||||||
| chr6:129626105
|
C | CACACACA others(5): Show |
14 | a0001c0001t0001g0090a0001c0001t0001g0098a0001c0001t0001g0101others(11): Show | 14 | HG00544.hp2 HG00733.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.786+3247_786+3248i others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626105 | ||||||
| chr6:129626105
|
C | CACACACA others(3): Show |
9 | a0001c0001t0001g0100a0001c0001t0001g0103a0001c0001t0001g0104others(6): Show | 9 | HG00621.hp1 HG00741.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.786+3247_786+3248i others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626105 | ||||||
| chr6:129626105
|
C | CACACATA others(1): Show |
13 | a0001c0001t0001g0094a0001c0001t0001g0106a0001c0001t0001g0116others(10): Show | 13 | HG00642.hp2 HG01074.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.786+3247_786+3248i others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626105 | ||||||
| chr6:129626105
|
C | T | 6 | a0001c0001t0001g0001a0001c0001t0005g0207a0001c0001t0009g0069others(3): Show | 7 | HG00597.hp2 HG00738.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.786+3248G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626105 | ||||||
| chr6:129626107
|
T | C | 2 | a0001c0001t0011g0141a0003c0004t0005g0088 | 2 | HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.786+3246A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626107 | ||||||
| chr6:129626297
|
G | A | 1 | a0001c0001t0001g0215 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.786+3056C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626297 | ||||||
| chr6:129626378
|
A | G | 1 | a0001c0001t0002g0185 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.786+2975T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626378 | ||||||
| chr6:129626441
|
T | A | 1 | a0001c0001t0003g0224 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.786+2912A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626441 | ||||||
| chr6:129626455
|
A | G | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.786+2898T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626455 | ||||||
| chr6:129626650
|
G | A | 11 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(8): Show | 11 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.786+2703C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626650 | ||||||
| chr6:129626655
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.786+2698G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626655 | ||||||
| chr6:129626672
|
T | TAC | 53 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0072others(50): Show | 53 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.786+2679_786+2680d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626672 | ||||||
| chr6:129626672
|
TAC | T | 18 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0067others(15): Show | 18 | HG00099.hp2 HG00423.hp1 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.786+2679_786+2680d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626672 | ||||||
| chr6:129626672
|
TACAC | T | 46 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(43): Show | 46 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.786+2677_786+2680d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626672 | ||||||
| chr6:129626672
|
TACACACA others(1): Show |
T | 53 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(50): Show | 54 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.786+2673_786+2680d others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626672 | ||||||
| chr6:129626702
|
C | A | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.786+2651G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626702 | ||||||
| chr6:129626706
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0136 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+2647A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129626706 | ||||||
| chr6:129627024
|
A | G | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+2329T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627024 | ||||||
| chr6:129627042
|
AACAGAAA others(7): Show |
A | 1 | a0001c0001t0001g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.786+2297_786+2310d others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627042 | ||||||
| chr6:129627053
|
T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0080others(97): Show | 101 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.786+2300A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627053 | ||||||
| chr6:129627112
|
G | T | 1 | a0001c0001t0001g0166 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.786+2241C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627112 | ||||||
| chr6:129627174
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.786+2179T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627174 | ||||||
| chr6:129627331
|
G | A | 51 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.786+2022C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627331 | ||||||
| chr6:129627343
|
A | G | 9 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(6): Show | 9 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.786+2010T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627343 | ||||||
| chr6:129627382
|
C | CA | 63 | a0001c0001t0001g0001a0001c0001t0001g0079a0001c0001t0001g0090others(60): Show | 64 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.786+1970dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627382 | ||||||
| chr6:129627446
|
G | A | 6 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(3): Show | 6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+1907C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627446 | ||||||
| chr6:129627485
|
G | A | 1 | a0002c0002t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.786+1868C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627485 | ||||||
| chr6:129627588
|
T | G | 1 | a0002c0002t0002g0042 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.786+1765A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627588 | ||||||
| chr6:129627715
|
A | G | 2 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786+1638T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627715 | ||||||
| chr6:129627867
|
T | A | 25 | a0001c0001t0001g0142a0001c0001t0001g0216a0001c0001t0001g0218others(22): Show | 25 | HG00408.hp2 HG00558.hp1 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.786+1486A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627867 | ||||||
| chr6:129627910
|
C | T | 6 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(3): Show | 6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.786+1443G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627910 | ||||||
| chr6:129627913
|
T | C | 1 | a0001c0001t0003g0224 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.786+1440A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627913 | ||||||
| chr6:129627986
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.786+1367G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129627986 | ||||||
| chr6:129628106
|
A | G | 1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.786+1247T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129628106 | ||||||
| chr6:129628560
|
C | A | 1 | a0001c0001t0002g0176 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.786+793G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129628560 | ||||||
| chr6:129628560
|
C | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(54): Show | 58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.786+793G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129628560 | ||||||
| chr6:129628864
|
G | A | 1 | a0002c0002t0002g0019 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.786+489C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129628864 | ||||||
| chr6:129628926
|
A | T | 57 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(54): Show | 58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.786+427T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129628926 | ||||||
| chr6:129628976
|
G | A | 1 | a0001c0001t0016g0149 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.786+377C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129628976 | ||||||
| chr6:129629199
|
C | T | 1 | a0002c0002t0001g0038 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.786+154G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629199 | ||||||
| chr6:129629221
|
C | G | 2 | a0001c0001t0001g0079a0001c0001t0001g0136 | 2 | HG02486.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.786+132G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629221 | ||||||
| chr6:129629233
|
G | GTC | 7 | a0001c0001t0001g0079a0001c0001t0001g0136a0001c0001t0002g0145others(4): Show | 7 | HG02451.hp1 HG02486.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.786+118_786+119dup others(2): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629233 | ||||||
| chr6:129629247
|
C | A | 3 | a0001c0001t0002g0125a0001c0001t0002g0223a0002c0002t0003g0023 | 3 | HG00558.hp1 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.786+106G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629247 | ||||||
| chr6:129629247
|
CTA | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(54): Show | 58 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.786+104_786+105del others(2): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629247 | ||||||
| chr6:129629249
|
A | C | 140 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0065others(137): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.786+104T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629249 | ||||||
| chr6:129629251
|
A | C | 37 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0090others(34): Show | 37 | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.786+102T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629251 | ||||||
| chr6:129629253
|
A | C | 11 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(8): Show | 11 | HG00423.hp1 HG02615.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.786+100T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629253 | ||||||
| chr6:129629255
|
A | C | 2 | a0001c0001t0003g0138a0001c0001t0011g0141 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.786+98T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629255 | ||||||
| chr6:129629261
|
A | G | 36 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0079others(33): Show | 36 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.786+92T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629261 | ||||||
| chr6:129629268
|
T | C | 1 | a0001c0001t0001g0213 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.786+85A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | 129629268 | ||||||
| chr6:129629581
|
T | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | HG00140.hp1 HG00735.hp1 |
intron_variant | MODIFIER | c.617-59A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129629581 | ||||||
| chr6:129629619
|
T | C | 10 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(7): Show | 10 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.617-97A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129629619 | ||||||
| chr6:129629646
|
C | T | 3 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0177 | 3 | HG01433.hp1 HG01928.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.617-124G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129629646 | ||||||
| chr6:129630064
|
G | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(57): Show | 61 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.617-542C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630064 | ||||||
| chr6:129630077
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0136a0002c0002t0001g0044 | 3 | HG02486.hp1 HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.617-555C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630077 | ||||||
| chr6:129630095
|
C | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(55): Show | 59 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.617-573G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630095 | ||||||
| chr6:129630312
|
T | C | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.617-790A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630312 | ||||||
| chr6:129630386
|
A | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(55): Show | 59 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.617-864T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630386 | ||||||
| chr6:129630403
|
T | A | 3 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139 | 3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.617-881A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630403 | ||||||
| chr6:129630434
|
A | T | 9 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(6): Show | 9 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.617-912T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630434 | ||||||
| chr6:129630505
|
G | T | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.617-983C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630505 | ||||||
| chr6:129630662
|
A | G | 1 | a0001c0001t0002g0170 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.617-1140T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630662 | ||||||
| chr6:129630714
|
T | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(55): Show | 59 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.617-1192A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630714 | ||||||
| chr6:129630716
|
C | G | 58 | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(55): Show | 59 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.617-1194G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630716 | ||||||
| chr6:129630763
|
G | T | 1 | a0002c0002t0001g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.617-1241C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630763 | ||||||
| chr6:129630767
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.617-1245G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630767 | ||||||
| chr6:129630856
|
C | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0064others(125): Show | 129 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.617-1334G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630856 | ||||||
| chr6:129630869
|
T | C | 6 | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(3): Show | 6 | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.617-1347A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630869 | ||||||
| chr6:129630983
|
T | C | 10 | a0001c0001t0002g0082a0001c0001t0005g0207a0001c0001t0005g0212others(7): Show | 10 | HG00099.hp1 HG00597.hp2 HG03669.hp2 others(7): Show |
intron_variant | MODIFIER | c.617-1461A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129630983 | ||||||
| chr6:129631217
|
G | C | 1 | a0002c0002t0003g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.617-1695C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631217 | ||||||
| chr6:129631267
|
T | C | 64 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(61): Show | 65 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.617-1745A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631267 | ||||||
| chr6:129631334
|
G | A | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0099others(5): Show | 8 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.617-1812C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631334 | ||||||
| chr6:129631358
|
A | C | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.617-1836T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631358 | ||||||
| chr6:129631366
|
C | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0132 | 2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.617-1844G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631366 | ||||||
| chr6:129631392
|
C | CAA | 63 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(60): Show | 64 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.617-1872_617-1871d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631392 | ||||||
| chr6:129631485
|
G | C | 2 | a0001c0001t0003g0128a0002c0002t0003g0043 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.617-1963C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631485 | ||||||
| chr6:129631530
|
T | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(63): Show | 67 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.617-2008A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631530 | ||||||
| chr6:129631761
|
TTA | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(63): Show | 67 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.617-2241_617-2240d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631761 | ||||||
| chr6:129631762
|
T | A | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.617-2240A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631762 | ||||||
| chr6:129631762
|
T | TA | 33 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0067others(30): Show | 33 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(30): Show |
intron_variant | MODIFIER | c.617-2241dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631762 | ||||||
| chr6:129631762
|
T | TAA | 8 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0153others(5): Show | 8 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.617-2242_617-2241d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631762 | ||||||
| chr6:129631785
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.616+2257A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631785 | ||||||
| chr6:129631863
|
T | G | 3 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139 | 3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.616+2179A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631863 | ||||||
| chr6:129631896
|
C | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(62): Show | 66 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.616+2146G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631896 | ||||||
| chr6:129631941
|
G | GAATT | 67 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(64): Show | 68 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.616+2097_616+2100d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631941 | ||||||
| chr6:129631972
|
C | A | 1 | a0002c0002t0001g0031 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.616+2070G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129631972 | ||||||
| chr6:129632130
|
C | A | 63 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(60): Show | 64 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.616+1912G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129632130 | ||||||
| chr6:129632230
|
T | C | 1 | a0002c0002t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.616+1812A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129632230 | ||||||
| chr6:129632291
|
C | G | 1 | a0001c0001t0001g0111 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.616+1751G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129632291 | ||||||
| chr6:129632439
|
T | C | 1 | a0001c0001t0002g0181 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.616+1603A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129632439 | ||||||
| chr6:129632698
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.616+1344G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129632698 | ||||||
| chr6:129632766
|
A | G | 1 | a0002c0002t0001g0012 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.616+1276T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129632766 | ||||||
| chr6:129632781
|
G | C | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.616+1261C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129632781 | ||||||
| chr6:129632808
|
A | T | 2 | a0001c0001t0001g0079a0001c0001t0001g0132 | 2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.616+1234T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129632808 | ||||||
| chr6:129633124
|
T | C | 31 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(28): Show | 31 | HG00099.hp2 HG00408.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.616+918A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633124 | ||||||
| chr6:129633136
|
A | G | 1 | a0001c0001t0003g0224 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.616+906T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633136 | ||||||
| chr6:129633231
|
C | T | 6 | a0001c0001t0001g0079a0001c0001t0001g0132a0001c0001t0007g0077others(3): Show | 6 | HG02280.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.616+811G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633231 | ||||||
| chr6:129633266
|
TA | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(129): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.616+775delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633266 | ||||||
| chr6:129633268
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.616+774T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633268 | ||||||
| chr6:129633285
|
A | T | 1 | a0002c0002t0003g0037 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.616+757T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633285 | ||||||
| chr6:129633371
|
G | A | 19 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(16): Show | 19 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.616+671C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633371 | ||||||
| chr6:129633431
|
C | T | 1 | a0003c0004t0005g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.616+611G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633431 | ||||||
| chr6:129633434
|
C | CAA | 83 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(80): Show |
intron_variant | MODIFIER | c.616+606_616+607dup others(2): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633434 | ||||||
| chr6:129633434
|
C | CAAA | 39 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(36): Show | 40 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.616+605_616+607dup others(3): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633434 | ||||||
| chr6:129633772
|
G | A | 3 | a0001c0001t0002g0145a0001c0001t0010g0137a0003c0004t0001g0151 | 3 | HG02451.hp1 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.616+270C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633772 | ||||||
| chr6:129633829
|
C | T | 2 | a0001c0011t0001g0056a0003c0004t0005g0088 | 2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.616+213G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633829 | ||||||
| chr6:129633908
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.616+134G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633908 | ||||||
| chr6:129633972
|
A | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(108): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.616+70T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633972 | ||||||
| chr6:129633989
|
A | C | 1 | a0001c0001t0002g0171 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.616+53T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129633989 | ||||||
| chr6:129634006
|
G | GA | 74 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(71): Show | 75 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.616+35dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129634006 | ||||||
| chr6:129634006
|
GA | G | 5 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076others(2): Show | 5 | HG00609.hp1 HG01081.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.616+35delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129634006 | ||||||
| chr6:129634026
|
A | G | 10 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0153others(7): Show | 10 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.616+16T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | 129634026 | ||||||
| chr6:129634159
|
T | C | 1 | a0002c0002t0001g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.553-54A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634159 | ||||||
| chr6:129634182
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(70): Show | 74 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.553-77A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634182 | ||||||
| chr6:129634342
|
C | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(68): Show | 72 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.553-237G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634342 | ||||||
| chr6:129634368
|
C | T | 2 | a0001c0001t0002g0125a0001c0001t0002g0223 | 2 | HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.553-263G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634368 | ||||||
| chr6:129634379
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.553-274C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634379 | ||||||
| chr6:129634679
|
T | A | 1 | a0001c0001t0002g0145 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.553-574A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634679 | ||||||
| chr6:129634681
|
T | C | 5 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(2): Show | 5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.553-576A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634681 | ||||||
| chr6:129634781
|
T | C | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.553-676A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634781 | ||||||
| chr6:129634847
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0002g0113 | 2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.553-742T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634847 | ||||||
| chr6:129634888
|
T | TA | 63 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(60): Show | 64 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.553-784dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634888 | ||||||
| chr6:129634888
|
TA | T | 31 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0108others(28): Show | 31 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.553-784delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634888 | ||||||
| chr6:129634926
|
AC | A | 3 | a0002c0002t0001g0035a0002c0002t0001g0036a0009c0007t0001g0030 | 3 | HG00408.hp1 HG02132.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.553-822delG | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634926 | ||||||
| chr6:129634974
|
C | T | 30 | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(27): Show | 30 | HG00140.hp2 HG00408.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.553-869G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634974 | ||||||
| chr6:129634992
|
G | A | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.553-887C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129634992 | ||||||
| chr6:129635011
|
C | T | 5 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(2): Show | 5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.553-906G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129635011 | ||||||
| chr6:129635246
|
A | G | 2 | a0001c0011t0001g0056a0003c0004t0005g0088 | 2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.553-1141T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129635246 | ||||||
| chr6:129635331
|
G | A | 2 | a0001c0011t0001g0056a0003c0004t0005g0088 | 2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.553-1226C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129635331 | ||||||
| chr6:129635485
|
C | T | 3 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0011t0001g0056 | 3 | HG02896.hp1 HG02897.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.553-1380G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129635485 | ||||||
| chr6:129635709
|
C | T | 2 | a0001c0001t0001g0164a0001c0011t0001g0056 | 2 | HG03209.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.553-1604G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129635709 | ||||||
| chr6:129635835
|
T | C | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.553-1730A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129635835 | ||||||
| chr6:129635900
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.553-1795G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129635900 | ||||||
| chr6:129636185
|
GTAAGCAA others(10): Show |
G | 1 | a0001c0001t0001g0163 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.553-2097_553-2081d others(19): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636185 | ||||||
| chr6:129636208
|
AAG | A | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.553-2105_553-2104d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636208 | ||||||
| chr6:129636408
|
A | G | 2 | a0001c0001t0008g0118a0001c0001t0008g0228 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.552+1986T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636408 | ||||||
| chr6:129636488
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.552+1906G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636488 | ||||||
| chr6:129636586
|
T | C | 8 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0153others(5): Show | 8 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.552+1808A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636586 | ||||||
| chr6:129636605
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.552+1789C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636605 | ||||||
| chr6:129636771
|
C | T | 2 | a0001c0011t0001g0056a0003c0004t0005g0088 | 2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.552+1623G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636771 | ||||||
| chr6:129636808
|
G | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.552+1586C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636808 | ||||||
| chr6:129636809
|
G | A | 1 | a0001c0001t0015g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.552+1585C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636809 | ||||||
| chr6:129636907
|
T | C | 5 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0076others(2): Show | 5 | HG00609.hp1 HG01081.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.552+1487A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636907 | ||||||
| chr6:129636977
|
C | T | 5 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(2): Show | 5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.552+1417G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129636977 | ||||||
| chr6:129637188
|
G | A | 1 | a0002c0002t0006g0032 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.552+1206C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129637188 | ||||||
| chr6:129637210
|
A | G | 3 | a0001c0001t0001g0209a0002c0002t0001g0007a0002c0002t0001g0018 | 3 | HG00621.hp2 NA18962.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.552+1184T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129637210 | ||||||
| chr6:129637257
|
G | A | 2 | a0001c0001t0002g0182a0001c0001t0002g0185 | 2 | HG01074.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.552+1137C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129637257 | ||||||
| chr6:129637345
|
G | A | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.552+1049C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129637345 | ||||||
| chr6:129637524
|
C | T | 5 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(2): Show | 5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.552+870G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129637524 | ||||||
| chr6:129637550
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.552+844T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129637550 | ||||||
| chr6:129637620
|
C | A | 2 | a0001c0001t0001g0126a0002c0002t0001g0025 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.552+774G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129637620 | ||||||
| chr6:129637676
|
A | G | 1 | a0001c0001t0002g0120 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.552+718T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129637676 | ||||||
| chr6:129637952
|
C | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(50): Show | 54 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.552+442G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129637952 | ||||||
| chr6:129638130
|
C | G | 1 | a0001c0001t0003g0224 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.552+264G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129638130 | ||||||
| chr6:129638141
|
C | A | 2 | a0001c0001t0001g0112a0001c0001t0002g0113 | 2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.552+253G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129638141 | ||||||
| chr6:129638272
|
G | T | 2 | a0001c0001t0002g0145a0003c0004t0001g0151 | 2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.552+122C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 3/14 | chr6 | 129638272 | ||||||
| chr6:129638742
|
C | T | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.317-113G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129638742 | ||||||
| chr6:129638868
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.317-239T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129638868 | ||||||
| chr6:129639161
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(52): Show | 56 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.317-532C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639161 | ||||||
| chr6:129639192
|
GT | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(52): Show | 56 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.317-564delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639192 | ||||||
| chr6:129639223
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(52): Show | 56 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.317-594T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639223 | ||||||
| chr6:129639231
|
A | C | 2 | a0001c0001t0008g0118a0001c0001t0008g0228 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.317-602T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639231 | ||||||
| chr6:129639236
|
G | T | 2 | a0001c0001t0008g0118a0001c0001t0008g0228 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.317-607C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639236 | ||||||
| chr6:129639351
|
T | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(52): Show | 56 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.317-722A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639351 | ||||||
| chr6:129639389
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(52): Show | 56 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.317-760C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639389 | ||||||
| chr6:129639470
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.317-841C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639470 | ||||||
| chr6:129639555
|
T | C | 1 | a0001c0001t0001g0180 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.317-926A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639555 | ||||||
| chr6:129639630
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.317-1001A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639630 | ||||||
| chr6:129639649
|
G | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0132 | 2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.317-1020C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639649 | ||||||
| chr6:129639714
|
C | T | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.317-1085G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639714 | ||||||
| chr6:129639716
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.317-1087G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639716 | ||||||
| chr6:129639732
|
C | G | 5 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(2): Show | 5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-1103G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639732 | ||||||
| chr6:129639994
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(52): Show | 56 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.317-1365C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639994 | ||||||
| chr6:129639999
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.317-1370A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129639999 | ||||||
| chr6:129640023
|
C | T | 24 | a0001c0001t0001g0080a0001c0001t0001g0136a0001c0001t0001g0206others(21): Show | 24 | HG00408.hp2 HG00642.hp1 HG02071.hp1 others(21): Show |
intron_variant | MODIFIER | c.317-1394G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640023 | ||||||
| chr6:129640042
|
C | CA | 39 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0079others(36): Show | 39 | HG00408.hp2 HG00438.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.317-1414dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640042 | ||||||
| chr6:129640042
|
C | CAA | 10 | a0001c0001t0001g0064a0001c0001t0001g0099a0001c0001t0001g0179others(7): Show | 10 | HG00735.hp2 HG01433.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.317-1415_317-1414d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640042 | ||||||
| chr6:129640042
|
CAAAA | C | 49 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(46): Show | 50 | HG00140.hp1 HG00609.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.317-1417_317-1414d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640042 | ||||||
| chr6:129640059
|
A | C | 2 | a0001c0011t0001g0056a0003c0004t0005g0088 | 2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.317-1430T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640059 | ||||||
| chr6:129640065
|
C | A | 49 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(46): Show | 49 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.317-1436G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640065 | ||||||
| chr6:129640069
|
C | A | 10 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(7): Show | 10 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.317-1440G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640069 | ||||||
| chr6:129640104
|
A | G | 49 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(46): Show | 49 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(46): Show |
intron_variant | MODIFIER | c.317-1475T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640104 | ||||||
| chr6:129640287
|
T | C | 2 | a0001c0001t0001g0079a0001c0001t0001g0132 | 2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.316+1529A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640287 | ||||||
| chr6:129640398
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.316+1418T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640398 | ||||||
| chr6:129640605
|
C | T | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.316+1211G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640605 | ||||||
| chr6:129640618
|
T | C | 2 | a0001c0001t0002g0145a0003c0004t0001g0151 | 2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.316+1198A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640618 | ||||||
| chr6:129640693
|
G | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(72): Show | 76 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.316+1123C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640693 | ||||||
| chr6:129640829
|
A | C | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.316+987T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640829 | ||||||
| chr6:129640831
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(72): Show | 76 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.316+985C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640831 | ||||||
| chr6:129640986
|
T | C | 14 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(11): Show | 14 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.316+830A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640986 | ||||||
| chr6:129640991
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.316+825C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129640991 | ||||||
| chr6:129641156
|
G | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(72): Show | 76 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.316+660C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129641156 | ||||||
| chr6:129641247
|
T | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(72): Show | 76 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.316+569A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129641247 | ||||||
| chr6:129641322
|
T | C | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.316+494A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129641322 | ||||||
| chr6:129641338
|
A | G | 2 | a0001c0001t0001g0126a0002c0002t0001g0025 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.316+478T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129641338 | ||||||
| chr6:129641445
|
C | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(72): Show | 76 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.316+371G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129641445 | ||||||
| chr6:129641488
|
T | C | 75 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(72): Show | 76 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.316+328A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129641488 | ||||||
| chr6:129641612
|
T | C | 3 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139 | 3 | HG02622.hp1 HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.316+204A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129641612 | ||||||
| chr6:129641728
|
A | AT | 21 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0079others(18): Show | 21 | HG00099.hp2 HG00735.hp2 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.316+87dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129641728 | ||||||
| chr6:129641786
|
C | A | 20 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(17): Show | 20 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.316+30G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 2/14 | chr6 | 129641786 | ||||||
| chr6:129642574
|
G | A | 53 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(50): Show | 54 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.114-556C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129642574 | ||||||
| chr6:129642577
|
T | C | 5 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(2): Show | 5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-559A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129642577 | ||||||
| chr6:129642702
|
A | G | 1 | a0002c0002t0003g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.114-684T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129642702 | ||||||
| chr6:129642825
|
C | T | 2 | a0001c0011t0001g0056a0003c0004t0005g0088 | 2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.114-807G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129642825 | ||||||
| chr6:129642827
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.114-809C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129642827 | ||||||
| chr6:129642907
|
C | A | 93 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(90): Show | 94 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.114-889G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129642907 | ||||||
| chr6:129642917
|
A | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(74): Show | 78 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.114-899T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129642917 | ||||||
| chr6:129643155
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.114-1137A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129643155 | ||||||
| chr6:129643226
|
G | A | 5 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(2): Show | 5 | HG02622.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-1208C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129643226 | ||||||
| chr6:129643293
|
C | A | 1 | a0001c0001t0003g0224 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.114-1275G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129643293 | ||||||
| chr6:129643297
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.114-1279G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129643297 | ||||||
| chr6:129643303
|
G | T | 1 | a0001c0001t0015g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.114-1285C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129643303 | ||||||
| chr6:129643857
|
C | G | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.114-1839G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129643857 | ||||||
| chr6:129643861
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.114-1843C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129643861 | ||||||
| chr6:129643931
|
A | T | 2 | a0001c0011t0001g0056a0003c0004t0005g0088 | 2 | HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.114-1913T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129643931 | ||||||
| chr6:129643998
|
T | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | HG00735.hp2 HG01106.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.114-1980A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129643998 | ||||||
| chr6:129644209
|
G | A | 56 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(53): Show | 57 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.114-2191C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129644209 | ||||||
| chr6:129644287
|
A | G | 4 | a0001c0001t0001g0090a0001c0001t0001g0101a0001c0001t0007g0077others(1): Show | 4 | HG01361.hp2 HG01981.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-2269T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129644287 | ||||||
| chr6:129644359
|
A | G | 1 | a0003c0004t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.114-2341T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129644359 | ||||||
| chr6:129644388
|
T | A | 17 | a0001c0001t0001g0098a0001c0001t0001g0129a0001c0001t0001g0155others(14): Show | 17 | HG00544.hp2 HG00609.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.114-2370A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129644388 | ||||||
| chr6:129644388
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.114-2370A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129644388 | ||||||
| chr6:129644421
|
A | G | 6 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(3): Show | 6 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.114-2403T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129644421 | ||||||
| chr6:129644547
|
TTC | T | 18 | a0001c0001t0001g0079a0001c0001t0001g0142a0001c0001t0002g0145others(15): Show | 18 | HG01192.hp2 HG02451.hp1 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.114-2531_114-2530d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129644547 | ||||||
| chr6:129644983
|
A | G | 1 | a0001c0001t0002g0117 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.114-2965T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129644983 | ||||||
| chr6:129645021
|
T | C | 2 | a0002c0002t0001g0016a0002c0002t0001g0017 | 2 | HG01175.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.114-3003A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645021 | ||||||
| chr6:129645202
|
G | T | 11 | a0001c0001t0001g0079a0001c0001t0002g0145a0001c0001t0003g0224others(8): Show | 11 | HG02451.hp1 HG02622.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.114-3184C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645202 | ||||||
| chr6:129645205
|
ACTT | A | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | NA18986.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.114-3190_114-3188d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645205 | ||||||
| chr6:129645260
|
A | G | 20 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(17): Show | 20 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.114-3242T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645260 | ||||||
| chr6:129645268
|
G | A | 22 | a0001c0001t0001g0080a0001c0001t0001g0136a0001c0001t0001g0206others(19): Show | 22 | HG00408.hp2 HG00642.hp1 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.114-3250C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645268 | ||||||
| chr6:129645300
|
A | G | 3 | a0001c0001t0003g0237a0002c0002t0001g0044a0002c0002t0014g0045 | 3 | HG02257.hp2 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.114-3282T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645300 | ||||||
| chr6:129645391
|
T | C | 22 | a0001c0001t0001g0080a0001c0001t0001g0136a0001c0001t0001g0206others(19): Show | 22 | HG00408.hp2 HG00642.hp1 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.114-3373A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645391 | ||||||
| chr6:129645457
|
T | A | 1 | a0002c0002t0001g0038 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.114-3439A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645457 | ||||||
| chr6:129645515
|
C | A | 90 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(87): Show | 91 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.114-3497G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645515 | ||||||
| chr6:129645542
|
C | T | 5 | a0001c0001t0002g0145a0001c0001t0004g0123a0001c0001t0004g0134others(2): Show | 5 | HG02451.hp1 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-3524G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645542 | ||||||
| chr6:129645570
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(52): Show | 56 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.114-3552T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645570 | ||||||
| chr6:129645637
|
G | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(100): Show | 104 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.114-3619C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645637 | ||||||
| chr6:129645762
|
C | CT | 26 | a0001c0001t0001g0080a0001c0001t0001g0136a0001c0001t0001g0206others(23): Show | 26 | HG00408.hp2 HG00642.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.114-3745dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645762 | ||||||
| chr6:129645775
|
G | A | 8 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0153others(5): Show | 8 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-3757C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129645775 | ||||||
| chr6:129646078
|
A | G | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 8 | HG00099.hp2 HG01433.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-4060T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129646078 | ||||||
| chr6:129646088
|
C | T | 4 | a0001c0001t0008g0118a0001c0001t0008g0228a0002c0002t0001g0006others(1): Show | 4 | HG02615.hp2 HG02922.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-4070G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129646088 | ||||||
| chr6:129646368
|
G | C | 2 | a0002c0002t0001g0006a0007c0008t0004g0055 | 2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-4350C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129646368 | ||||||
| chr6:129646460
|
C | T | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114-4442G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129646460 | ||||||
| chr6:129646555
|
A | T | 58 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(55): Show | 58 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.114-4537T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129646555 | ||||||
| chr6:129646823
|
C | T | 44 | a0001c0001t0001g0067a0001c0001t0001g0080a0001c0001t0001g0084others(41): Show | 44 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.114-4805G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129646823 | ||||||
| chr6:129646929
|
A | G | 2 | a0001c0011t0001g0056a0003c0004t0001g0151 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.114-4911T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129646929 | ||||||
| chr6:129646971
|
T | C | 2 | a0001c0011t0001g0056a0003c0004t0001g0151 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.114-4953A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129646971 | ||||||
| chr6:129647085
|
C | G | 1 | a0001c0001t0002g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.114-5067G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129647085 | ||||||
| chr6:129647221
|
T | A | 1 | a0002c0002t0014g0045 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.114-5203A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129647221 | ||||||
| chr6:129647335
|
T | C | 118 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(115): Show | 119 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(116): Show |
intron_variant | MODIFIER | c.114-5317A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129647335 | ||||||
| chr6:129647338
|
A | G | 129 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(126): Show | 130 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(127): Show |
intron_variant | MODIFIER | c.114-5320T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129647338 | ||||||
| chr6:129647347
|
A | G | 2 | a0001c0001t0008g0118a0001c0001t0008g0228 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-5329T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129647347 | ||||||
| chr6:129647487
|
T | C | 5 | a0001c0001t0002g0145a0001c0001t0004g0123a0001c0001t0004g0134others(2): Show | 5 | HG02451.hp1 HG02622.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-5469A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129647487 | ||||||
| chr6:129647673
|
TA | T | 26 | a0001c0001t0001g0080a0001c0001t0001g0103a0001c0001t0001g0132others(23): Show | 26 | HG00408.hp2 HG00642.hp1 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.114-5656delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129647673 | ||||||
| chr6:129647770
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.114-5752T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129647770 | ||||||
| chr6:129647996
|
T | G | 1 | a0001c0001t0001g0204 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.114-5978A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129647996 | ||||||
| chr6:129648012
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.114-5994G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648012 | ||||||
| chr6:129648164
|
T | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0202 | 3 | HG00423.hp1 NA19000.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.114-6146A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648164 | ||||||
| chr6:129648231
|
C | G | 1 | a0001c0001t0001g0090 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.114-6213G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648231 | ||||||
| chr6:129648265
|
G | A | 2 | a0002c0002t0001g0006a0007c0008t0004g0055 | 2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-6247C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648265 | ||||||
| chr6:129648284
|
A | G | 2 | a0002c0002t0001g0006a0007c0008t0004g0055 | 2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-6266T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648284 | ||||||
| chr6:129648445
|
T | C | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 8 | HG00099.hp2 HG01433.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-6427A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648445 | ||||||
| chr6:129648583
|
G | A | 2 | a0001c0001t0008g0118a0001c0001t0008g0228 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-6565C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648583 | ||||||
| chr6:129648610
|
TA | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(55): Show | 59 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.114-6593delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648610 | ||||||
| chr6:129648719
|
TTATCTC | T | 2 | a0002c0002t0001g0006a0007c0008t0004g0055 | 2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-6707_114-6702d others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648719 | ||||||
| chr6:129648733
|
GA | G | 59 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(56): Show | 59 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.114-6716delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648733 | ||||||
| chr6:129648766
|
A | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(121): Show | 125 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
intron_variant | MODIFIER | c.114-6748T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648766 | ||||||
| chr6:129648779
|
C | T | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114-6761G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129648779 | ||||||
| chr6:129649065
|
G | A | 60 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(57): Show | 60 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.114-7047C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649065 | ||||||
| chr6:129649079
|
C | A | 1 | a0002c0002t0006g0032 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.114-7061G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649079 | ||||||
| chr6:129649137
|
A | G | 1 | a0001c0001t0001g0166 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.114-7119T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649137 | ||||||
| chr6:129649187
|
T | G | 2 | a0001c0001t0008g0118a0001c0001t0008g0228 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-7169A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649187 | ||||||
| chr6:129649269
|
G | A | 20 | a0001c0001t0001g0098a0001c0001t0001g0155a0001c0001t0001g0156others(17): Show | 20 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.114-7251C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649269 | ||||||
| chr6:129649422
|
C | T | 25 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(22): Show | 25 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.114-7404G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649422 | ||||||
| chr6:129649427
|
G | A | 2 | a0001c0001t0008g0118a0001c0001t0008g0228 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-7409C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649427 | ||||||
| chr6:129649462
|
G | A | 10 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(7): Show | 10 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.114-7444C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649462 | ||||||
| chr6:129649553
|
C | CA | 41 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0074others(38): Show | 41 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.114-7536dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649553 | ||||||
| chr6:129649553
|
C | CAA | 24 | a0001c0001t0001g0132a0001c0001t0001g0158a0001c0001t0001g0177others(21): Show | 24 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.114-7537_114-7536d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649553 | ||||||
| chr6:129649553
|
C | CAAA | 15 | a0001c0001t0001g0080a0001c0001t0001g0216a0001c0001t0001g0218others(12): Show | 15 | HG00597.hp2 HG00642.hp1 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.114-7538_114-7536d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649553 | ||||||
| chr6:129649553
|
CAA | C | 5 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(2): Show | 5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-7537_114-7536d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649553 | ||||||
| chr6:129649817
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(117): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.114-7799G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649817 | ||||||
| chr6:129649882
|
G | A | 55 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(52): Show | 56 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.114-7864C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649882 | ||||||
| chr6:129649904
|
CT | C | 5 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(2): Show | 5 | HG02622.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-7887delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649904 | ||||||
| chr6:129649913
|
T | G | 21 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(18): Show | 21 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.114-7895A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649913 | ||||||
| chr6:129649914
|
G | GT | 62 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0090others(59): Show | 63 | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.114-7897dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649914 | ||||||
| chr6:129649914
|
G | GTT | 33 | a0001c0001t0001g0062a0001c0001t0001g0080a0001c0001t0001g0132others(30): Show | 33 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.114-7898_114-7897d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649914 | ||||||
| chr6:129649914
|
G | GTTT | 5 | a0001c0001t0001g0206a0001c0001t0001g0221a0001c0001t0002g0181others(2): Show | 5 | HG02071.hp1 NA18944.hp2 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-7899_114-7897d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649914 | ||||||
| chr6:129649914
|
G | T | 21 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(18): Show | 21 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.114-7896C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649914 | ||||||
| chr6:129649981
|
C | T | 3 | a0001c0001t0008g0118a0001c0001t0008g0228a0007c0008t0004g0055 | 3 | HG02615.hp2 HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-7963G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649981 | ||||||
| chr6:129649990
|
A | G | 236 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(233): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.114-7972T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129649990 | ||||||
| chr6:129650079
|
A | AT | 93 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(90): Show | 94 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.114-8062dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650079 | ||||||
| chr6:129650079
|
AT | A | 26 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(23): Show | 26 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.114-8062delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650079 | ||||||
| chr6:129650151
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.114-8133G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650151 | ||||||
| chr6:129650316
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.114-8298G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650316 | ||||||
| chr6:129650343
|
G | A | 1 | a0001c0001t0002g0152 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.114-8325C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650343 | ||||||
| chr6:129650399
|
G | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(91): Show | 95 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.114-8381C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650399 | ||||||
| chr6:129650631
|
T | TA | 3 | a0001c0001t0019g0233a0002c0002t0001g0006a0007c0008t0004g0055 | 3 | HG02615.hp2 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.114-8614dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650631 | ||||||
| chr6:129650717
|
C | A | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-8699G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650717 | ||||||
| chr6:129650784
|
C | T | 53 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(50): Show | 54 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.114-8766G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650784 | ||||||
| chr6:129650915
|
C | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(58): Show | 62 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.114-8897G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650915 | ||||||
| chr6:129650931
|
T | C | 2 | a0002c0002t0001g0052a0002c0002t0001g0053 | 2 | HG02622.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.114-8913A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129650931 | ||||||
| chr6:129651170
|
T | TAA | 10 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(7): Show | 10 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.114-9154_114-9153d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129651170 | ||||||
| chr6:129651171
|
A | AAG | 16 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(13): Show | 16 | HG00099.hp2 HG01074.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.114-9155_114-9154d others(4): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129651171 | ||||||
| chr6:129651271
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.114-9253C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129651271 | ||||||
| chr6:129651463
|
C | T | 1 | a0003c0004t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.114-9445G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129651463 | ||||||
| chr6:129651780
|
A | G | 53 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(50): Show | 54 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.114-9762T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129651780 | ||||||
| chr6:129651832
|
T | C | 4 | a0001c0001t0001g0129a0001c0001t0001g0150a0001c0001t0001g0154others(1): Show | 4 | HG00558.hp2 NA18942.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-9814A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129651832 | ||||||
| chr6:129651884
|
GA | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.114-9867delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129651884 | ||||||
| chr6:129651920
|
T | A | 77 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.114-9902A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129651920 | ||||||
| chr6:129651985
|
C | T | 1 | a0002c0002t0001g0040 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.114-9967G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129651985 | ||||||
| chr6:129652003
|
G | A | 18 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(15): Show | 18 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.114-9985C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652003 | ||||||
| chr6:129652073
|
C | T | 5 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(2): Show | 5 | HG01192.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-10055G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652073 | ||||||
| chr6:129652102
|
G | T | 77 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(74): Show | 78 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.114-10084C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652102 | ||||||
| chr6:129652179
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.114-10161A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652179 | ||||||
| chr6:129652344
|
A | G | 1 | a0001c0001t0002g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.114-10326T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652344 | ||||||
| chr6:129652698
|
T | C | 44 | a0001c0001t0001g0080a0001c0001t0001g0132a0001c0001t0001g0142others(41): Show | 44 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.114-10680A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652698 | ||||||
| chr6:129652735
|
C | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.114-10717G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652735 | ||||||
| chr6:129652800
|
C | G | 2 | a0001c0001t0019g0233a0002c0002t0001g0006 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.114-10782G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652800 | ||||||
| chr6:129652817
|
A | T | 79 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.114-10799T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652817 | ||||||
| chr6:129652935
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.114-10917A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652935 | ||||||
| chr6:129652969
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(112): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.114-10951A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129652969 | ||||||
| chr6:129653037
|
A | T | 18 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(15): Show | 18 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.114-11019T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129653037 | ||||||
| chr6:129653112
|
C | A | 1 | a0002c0002t0001g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.114-11094G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129653112 | ||||||
| chr6:129653286
|
A | C | 1 | a0002c0002t0001g0012 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.114-11268T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129653286 | ||||||
| chr6:129653550
|
G | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(58): Show | 62 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.114-11532C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129653550 | ||||||
| chr6:129653622
|
A | G | 2 | a0001c0001t0008g0118a0001c0001t0008g0228 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-11604T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129653622 | ||||||
| chr6:129653701
|
G | A | 36 | a0001c0001t0001g0080a0001c0001t0001g0132a0001c0001t0001g0206others(33): Show | 36 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.114-11683C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129653701 | ||||||
| chr6:129653817
|
T | A | 1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.114-11799A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129653817 | ||||||
| chr6:129653822
|
A | AG | 55 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(52): Show | 56 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.114-11805dupC | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129653822 | ||||||
| chr6:129653823
|
G | GA | 24 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(21): Show | 24 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.114-11806dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129653823 | ||||||
| chr6:129654703
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.114-12685C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129654703 | ||||||
| chr6:129655045
|
G | A | 1 | a0002c0002t0001g0018 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.114-13027C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655045 | ||||||
| chr6:129655091
|
C | T | 2 | a0001c0001t0008g0118a0001c0001t0008g0228 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-13073G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655091 | ||||||
| chr6:129655119
|
G | A | 10 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0153others(7): Show | 10 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.114-13101C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655119 | ||||||
| chr6:129655123
|
C | T | 1 | a0001c0001t0006g0198 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.114-13105G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655123 | ||||||
| chr6:129655159
|
A | G | 55 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(52): Show | 56 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.114-13141T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655159 | ||||||
| chr6:129655211
|
C | T | 55 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(52): Show | 56 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.114-13193G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655211 | ||||||
| chr6:129655235
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.114-13217G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655235 | ||||||
| chr6:129655317
|
CA | C | 48 | a0001c0001t0001g0001a0001c0001t0001g0062a0001c0001t0001g0090others(45): Show | 49 | HG00423.hp2 HG00621.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.114-13300delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655317 | ||||||
| chr6:129655317
|
CAA | C | 5 | a0001c0001t0001g0131a0001c0001t0001g0194a0001c0001t0017g0174others(2): Show | 5 | HG00558.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-13301_114-1330 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655317 | ||||||
| chr6:129655332
|
A | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0062a0001c0001t0001g0090others(24): Show | 28 | HG00621.hp1 HG00642.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.114-13314T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655332 | ||||||
| chr6:129655332
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0009g0071 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.114-13324_114-1331 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655332 | ||||||
| chr6:129655333
|
AAAAAAAA others(2): Show |
A | 34 | a0001c0001t0001g0080a0001c0001t0001g0132a0001c0001t0001g0206others(31): Show | 34 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.114-13324_114-1331 others(13): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655333 | ||||||
| chr6:129655337
|
A | AG | 2 | a0001c0001t0019g0233a0002c0002t0001g0006 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.114-13320_114-1331 others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655337 | ||||||
| chr6:129655337
|
A | G | 63 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(60): Show | 64 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.114-13319T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655337 | ||||||
| chr6:129655337
|
AAAAAG | A | 8 | a0001c0001t0001g0063a0001c0001t0001g0084a0001c0001t0001g0091others(5): Show | 8 | HG02004.hp2 HG02486.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-13324_114-1332 others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655337 | ||||||
| chr6:129655338
|
AAAAG | A | 9 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0199others(6): Show | 9 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.114-13324_114-1332 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655338 | ||||||
| chr6:129655353
|
AAAAG | A | 8 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(5): Show | 8 | HG01192.hp2 HG02615.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-13339_114-1333 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655353 | ||||||
| chr6:129655371
|
G | A | 1 | a0002c0002t0001g0005 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.114-13353C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655371 | ||||||
| chr6:129655373
|
C | T | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.114-13355G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655373 | ||||||
| chr6:129655649
|
C | CATG | 36 | a0001c0001t0001g0080a0001c0001t0001g0132a0001c0001t0001g0206others(33): Show | 36 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.114-13632_114-1363 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655649 | ||||||
| chr6:129655932
|
C | T | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.114-13914G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655932 | ||||||
| chr6:129655943
|
T | G | 8 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0153others(5): Show | 8 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-13925A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655943 | ||||||
| chr6:129655956
|
G | A | 1 | a0002c0002t0001g0047 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.114-13938C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129655956 | ||||||
| chr6:129656004
|
T | C | 1 | a0001c0001t0002g0173 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.114-13986A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656004 | ||||||
| chr6:129656415
|
G | A | 6 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0004g0123others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.114-14397C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656415 | ||||||
| chr6:129656510
|
A | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(122): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.114-14492T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656510 | ||||||
| chr6:129656512
|
G | A | 4 | a0001c0001t0001g0105a0001c0001t0001g0187a0001c0001t0001g0196others(1): Show | 4 | NA18979.hp2 NA18999.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.114-14494C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656512 | ||||||
| chr6:129656622
|
C | T | 36 | a0001c0001t0001g0080a0001c0001t0001g0132a0001c0001t0001g0206others(33): Show | 36 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.114-14604G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656622 | ||||||
| chr6:129656642
|
TC | T | 18 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(15): Show | 18 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.114-14625delG | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656642 | ||||||
| chr6:129656668
|
TA | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(66): Show | 70 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.114-14651delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656668 | ||||||
| chr6:129656668
|
TAA | T | 10 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(7): Show | 10 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.114-14652_114-1465 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656668 | ||||||
| chr6:129656764
|
C | G | 36 | a0001c0001t0001g0080a0001c0001t0001g0132a0001c0001t0001g0206others(33): Show | 36 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.114-14746G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656764 | ||||||
| chr6:129656774
|
C | T | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.114-14756G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656774 | ||||||
| chr6:129656783
|
T | C | 2 | a0001c0001t0019g0233a0002c0002t0001g0006 | 2 | NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.114-14765A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656783 | ||||||
| chr6:129656813
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.114-14795T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656813 | ||||||
| chr6:129656938
|
T | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(52): Show | 56 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.114-14920A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129656938 | ||||||
| chr6:129657123
|
T | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(122): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.114-15105A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657123 | ||||||
| chr6:129657145
|
C | T | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 8 | HG00099.hp2 HG01074.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-15127G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657145 | ||||||
| chr6:129657251
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.114-15233A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657251 | ||||||
| chr6:129657260
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.114-15242A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657260 | ||||||
| chr6:129657378
|
T | C | 2 | a0001c0001t0001g0126a0002c0002t0001g0025 | 2 | HG02257.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.114-15360A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657378 | ||||||
| chr6:129657429
|
T | TAA | 20 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(17): Show | 20 | HG00099.hp2 HG00423.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.114-15413_114-1541 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657429 | ||||||
| chr6:129657429
|
T | TAAA | 58 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(55): Show | 59 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.114-15414_114-1541 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657429 | ||||||
| chr6:129657430
|
A | T | 3 | a0001c0001t0001g0177a0001c0001t0001g0201a0001c0001t0001g0213 | 3 | HG01358.hp2 HG01928.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.114-15412T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657430 | ||||||
| chr6:129657446
|
C | A | 1 | a0001c0001t0001g0091 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.114-15428G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657446 | ||||||
| chr6:129657447
|
A | T | 1 | a0002c0002t0003g0037 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.114-15429T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129657447 | ||||||
| chr6:129658009
|
T | C | 79 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(76): Show | 80 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.114-15991A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129658009 | ||||||
| chr6:129658422
|
G | GA | 22 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(19): Show | 22 | HG00099.hp2 HG00423.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.114-16405dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129658422 | ||||||
| chr6:129658422
|
GA | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(113): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.114-16405delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129658422 | ||||||
| chr6:129658593
|
A | T | 1 | a0002c0002t0003g0037 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.114-16575T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129658593 | ||||||
| chr6:129658617
|
C | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(58): Show | 62 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.114-16599G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129658617 | ||||||
| chr6:129658771
|
TAG | T | 2 | a0003c0004t0001g0151a0009c0007t0001g0030 | 2 | HG03098.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.114-16755_114-1675 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129658771 | ||||||
| chr6:129658804
|
A | T | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114-16786T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129658804 | ||||||
| chr6:129658931
|
G | T | 2 | a0001c0001t0009g0069a0001c0001t0009g0071 | 2 | NA18612.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.114-16913C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129658931 | ||||||
| chr6:129659065
|
C | G | 2 | a0001c0001t0008g0118a0001c0001t0008g0228 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-17047G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659065 | ||||||
| chr6:129659180
|
C | A | 1 | a0002c0002t0003g0037 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.114-17162G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659180 | ||||||
| chr6:129659291
|
T | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.114-17273A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659291 | ||||||
| chr6:129659307
|
T | C | 2 | a0001c0001t0003g0138a0001c0001t0011g0141 | 2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.114-17289A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659307 | ||||||
| chr6:129659456
|
T | A | 1 | a0001c0001t0001g0135 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.114-17438A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659456 | ||||||
| chr6:129659456
|
TTTTTA | T | 113 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(110): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.114-17443_114-1743 others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659456 | ||||||
| chr6:129659482
|
T | A | 1 | a0002c0002t0003g0037 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.114-17464A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659482 | ||||||
| chr6:129659483
|
A | T | 1 | a0002c0002t0003g0037 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.114-17465T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659483 | ||||||
| chr6:129659545
|
T | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(109): Show | 113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.114-17527A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659545 | ||||||
| chr6:129659660
|
T | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(118): Show | 122 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.114-17642A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659660 | ||||||
| chr6:129659660
|
T | G | 1 | a0002c0002t0003g0037 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.114-17642A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659660 | ||||||
| chr6:129659846
|
T | G | 4 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-17828A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659846 | ||||||
| chr6:129659919
|
C | T | 35 | a0001c0001t0001g0132a0001c0001t0001g0144a0001c0001t0001g0186others(32): Show | 35 | HG00408.hp2 HG00597.hp2 HG02071.hp1 others(32): Show |
intron_variant | MODIFIER | c.114-17901G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659919 | ||||||
| chr6:129659986
|
T | TG | 10 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0153others(7): Show | 10 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.114-17969dupC | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129659986 | ||||||
| chr6:129660068
|
A | G | 1 | a0002c0002t0003g0037 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.114-18050T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660068 | ||||||
| chr6:129660167
|
C | T | 1 | a0002c0002t0001g0012 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.114-18149G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660167 | ||||||
| chr6:129660170
|
CA | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0178 | 2 | HG00733.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.114-18153delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660170 | ||||||
| chr6:129660368
|
A | C | 1 | a0002c0002t0003g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.114-18350T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660368 | ||||||
| chr6:129660428
|
A | G | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.114-18410T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660428 | ||||||
| chr6:129660497
|
GA | G | 132 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(129): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.114-18480delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660497 | ||||||
| chr6:129660499
|
A | G | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 8 | HG00099.hp2 HG01074.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-18481T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660499 | ||||||
| chr6:129660752
|
T | A | 1 | a0001c0001t0002g0066 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.114-18734A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660752 | ||||||
| chr6:129660825
|
T | C | 5 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(2): Show | 5 | HG02895.hp1 HG02897.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-18807A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660825 | ||||||
| chr6:129660861
|
G | C | 85 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(82): Show | 86 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.114-18843C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660861 | ||||||
| chr6:129660893
|
T | G | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 8 | HG00099.hp2 HG01074.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-18875A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660893 | ||||||
| chr6:129660894
|
A | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(122): Show | 126 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(123): Show |
intron_variant | MODIFIER | c.114-18876T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129660894 | ||||||
| chr6:129661021
|
TA | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.114-19004delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661021 | ||||||
| chr6:129661108
|
C | T | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.114-19090G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661108 | ||||||
| chr6:129661140
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.114-19122T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661140 | ||||||
| chr6:129661256
|
C | G | 15 | a0001c0001t0001g0079a0001c0001t0001g0142a0001c0001t0001g0144others(12): Show | 15 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.114-19238G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661256 | ||||||
| chr6:129661298
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(88): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.114-19280A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661298 | ||||||
| chr6:129661309
|
T | TA | 131 | a0001c0001t0001g0001a0001c0001t0001g0062a0001c0001t0001g0072others(128): Show | 132 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.114-19292dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661309 | ||||||
| chr6:129661309
|
T | TAA | 10 | a0001c0001t0001g0108a0001c0001t0001g0157a0001c0001t0001g0179others(7): Show | 10 | HG00140.hp2 HG00544.hp1 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.114-19293_114-1929 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661309 | ||||||
| chr6:129661309
|
TA | T | 9 | a0001c0001t0001g0186a0001c0001t0001g0199a0001c0001t0001g0210others(6): Show | 9 | HG01074.hp1 HG02615.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.114-19292delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661309 | ||||||
| chr6:129661512
|
G | GA | 10 | a0001c0001t0001g0080a0001c0001t0001g0144a0001c0001t0002g0145others(7): Show | 10 | HG00642.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.114-19495dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661512 | ||||||
| chr6:129661512
|
G | GAA | 20 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(17): Show | 20 | HG00423.hp1 HG02074.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.114-19496_114-1949 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661512 | ||||||
| chr6:129661512
|
G | GAAA | 102 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(99): Show | 103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.114-19497_114-1949 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661512 | ||||||
| chr6:129661512
|
G | GAAAA | 10 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(7): Show | 10 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.114-19498_114-1949 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661512 | ||||||
| chr6:129661769
|
C | A | 67 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(64): Show | 68 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.114-19751G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661769 | ||||||
| chr6:129661972
|
C | CCA | 3 | a0001c0011t0001g0056a0003c0004t0001g0151a0003c0004t0005g0088 | 3 | HG03098.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.114-19956_114-1995 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661972 | ||||||
| chr6:129661972
|
CCA | C | 50 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(47): Show | 50 | HG00099.hp2 HG00408.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.114-19956_114-1995 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129661972 | ||||||
| chr6:129662223
|
A | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0202 | 3 | HG00423.hp1 NA19000.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.114-20205T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129662223 | ||||||
| chr6:129662229
|
C | T | 3 | a0001c0001t0001g0079a0001c0001t0007g0077a0001c0001t0007g0078 | 3 | HG02896.hp1 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.114-20211G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129662229 | ||||||
| chr6:129662385
|
T | G | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-20367A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129662385 | ||||||
| chr6:129662489
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.114-20471G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129662489 | ||||||
| chr6:129662498
|
G | A | 9 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(6): Show | 9 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.114-20480C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129662498 | ||||||
| chr6:129662727
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-20709A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129662727 | ||||||
| chr6:129662733
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-20715T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129662733 | ||||||
| chr6:129663078
|
T | G | 12 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(9): Show | 12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-21060A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129663078 | ||||||
| chr6:129663155
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-21137G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129663155 | ||||||
| chr6:129663210
|
A | G | 5 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0004g0123others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-21192T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129663210 | ||||||
| chr6:129663217
|
T | A | 116 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(113): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(114): Show |
intron_variant | MODIFIER | c.114-21199A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129663217 | ||||||
| chr6:129663450
|
A | G | 4 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0004g0123others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-21432T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129663450 | ||||||
| chr6:129663451
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.114-21433G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129663451 | ||||||
| chr6:129663670
|
C | A | 2 | a0001c0001t0004g0123a0001c0001t0004g0134 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.114-21652G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129663670 | ||||||
| chr6:129663748
|
A | C | 12 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(9): Show | 12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-21730T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129663748 | ||||||
| chr6:129663775
|
G | A | 1 | a0001c0001t0001g0209 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.114-21757C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129663775 | ||||||
| chr6:129664002
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(132): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.114-21984A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129664002 | ||||||
| chr6:129664025
|
A | T | 1 | a0002c0002t0001g0008 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.114-22007T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129664025 | ||||||
| chr6:129664079
|
T | A | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-22061A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129664079 | ||||||
| chr6:129664388
|
A | C | 5 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0004g0123others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-22370T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129664388 | ||||||
| chr6:129664505
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-22487C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129664505 | ||||||
| chr6:129664776
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.114-22758C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129664776 | ||||||
| chr6:129665219
|
A | G | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.114-23201T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665219 | ||||||
| chr6:129665283
|
G | A | 12 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(9): Show | 12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-23265C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665283 | ||||||
| chr6:129665308
|
C | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(98): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.114-23290G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665308 | ||||||
| chr6:129665325
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.114-23307C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665325 | ||||||
| chr6:129665344
|
G | A | 9 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(6): Show | 9 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.114-23326C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665344 | ||||||
| chr6:129665443
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.114-23425T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665443 | ||||||
| chr6:129665570
|
T | A | 5 | a0001c0001t0002g0125a0001c0001t0002g0223a0001c0001t0003g0224others(2): Show | 5 | HG02451.hp2 HG02630.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-23552A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665570 | ||||||
| chr6:129665619
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-23601G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665619 | ||||||
| chr6:129665647
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.114-23629A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665647 | ||||||
| chr6:129665660
|
G | A | 3 | a0001c0001t0003g0237a0002c0002t0001g0044a0002c0002t0014g0045 | 3 | HG02257.hp2 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.114-23642C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665660 | ||||||
| chr6:129665661
|
G | T | 15 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0084others(12): Show | 15 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.114-23643C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665661 | ||||||
| chr6:129665803
|
T | C | 1 | a0001c0001t0001g0136 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.114-23785A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129665803 | ||||||
| chr6:129666216
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-24198T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666216 | ||||||
| chr6:129666247
|
A | T | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.114-24229T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666247 | ||||||
| chr6:129666259
|
A | G | 2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.114-24241T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666259 | ||||||
| chr6:129666319
|
C | G | 1 | a0001c0001t0001g0194 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.114-24301G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666319 | ||||||
| chr6:129666347
|
C | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(56): Show | 60 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.114-24329G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666347 | ||||||
| chr6:129666396
|
C | T | 3 | a0001c0001t0001g0079a0001c0001t0007g0077a0001c0001t0007g0078 | 3 | HG02896.hp1 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.114-24378G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666396 | ||||||
| chr6:129666585
|
C | A | 1 | a0001c0001t0001g0163 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.114-24567G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666585 | ||||||
| chr6:129666699
|
C | T | 2 | a0001c0001t0008g0118a0001c0001t0008g0228 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-24681G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666699 | ||||||
| chr6:129666842
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.114-24824T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666842 | ||||||
| chr6:129666885
|
G | GC | 141 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.114-24868dupG | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666885 | ||||||
| chr6:129666944
|
T | C | 4 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-24926A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666944 | ||||||
| chr6:129666990
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.114-24972G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666990 | ||||||
| chr6:129666999
|
TA | T | 12 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(9): Show | 12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-24982delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129666999 | ||||||
| chr6:129667032
|
A | T | 2 | a0001c0001t0008g0118a0001c0001t0008g0228 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.114-25014T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667032 | ||||||
| chr6:129667054
|
T | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.114-25036A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667054 | ||||||
| chr6:129667055
|
T | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.114-25037A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667055 | ||||||
| chr6:129667056
|
C | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.114-25038G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667056 | ||||||
| chr6:129667198
|
AT | A | 5 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0004g0123others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-25181delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667198 | ||||||
| chr6:129667200
|
T | A | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.114-25182A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667200 | ||||||
| chr6:129667408
|
T | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.114-25390A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667408 | ||||||
| chr6:129667469
|
A | ATG | 14 | a0001c0001t0001g0086a0001c0001t0001g0111a0001c0001t0001g0124others(11): Show | 14 | HG00438.hp1 HG00639.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.114-25453_114-2545 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667469 | ||||||
| chr6:129667469
|
A | ATGTG | 5 | a0001c0001t0001g0188a0001c0001t0002g0081a0001c0001t0013g0119others(2): Show | 5 | HG01169.hp1 HG01169.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-25455_114-2545 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667469 | ||||||
| chr6:129667469
|
A | ATGTGTG | 2 | a0001c0001t0001g0127a0002c0002t0001g0040 | 2 | HG01175.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.114-25457_114-2545 others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667469 | ||||||
| chr6:129667469
|
A | G | 6 | a0001c0001t0003g0128a0001c0001t0003g0133a0001c0011t0001g0056others(3): Show | 6 | HG01261.hp1 HG03098.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.114-25451T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667469 | ||||||
| chr6:129667469
|
ATG | A | 6 | a0001c0001t0001g0085a0001c0001t0001g0147a0001c0001t0001g0158others(3): Show | 6 | HG00438.hp2 HG01358.hp2 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.114-25453_114-2545 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667469 | ||||||
| chr6:129667469
|
ATGTG | A | 25 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(22): Show | 25 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.114-25455_114-2545 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667469 | ||||||
| chr6:129667469
|
ATGTGTG | A | 2 | a0001c0001t0001g0214a0001c0001t0002g0162 | 2 | HG00544.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.114-25457_114-2545 others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667469 | ||||||
| chr6:129667492
|
T | C | 1 | a0001c0001t0004g0123 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.114-25474A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667492 | ||||||
| chr6:129667503
|
G | A | 25 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(22): Show | 25 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.114-25485C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667503 | ||||||
| chr6:129667503
|
G | GTA | 4 | a0001c0001t0002g0070a0001c0001t0008g0118a0001c0001t0008g0228others(1): Show | 4 | HG02717.hp1 HG02922.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-25486_114-2548 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667503 | ||||||
| chr6:129667503
|
G | GTGTA | 14 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(11): Show | 14 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.114-25486_114-2548 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667503 | ||||||
| chr6:129667503
|
G | GTGTGTA | 11 | a0001c0001t0001g0096a0001c0001t0001g0121a0001c0001t0001g0132others(8): Show | 11 | HG00733.hp1 HG01081.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.114-25486_114-2548 others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667503 | ||||||
| chr6:129667503
|
G | GTGTGTGT others(1): Show |
22 | a0001c0001t0001g0079a0001c0001t0001g0101a0001c0001t0001g0109others(19): Show | 22 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.114-25486_114-2548 others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667503 | ||||||
| chr6:129667503
|
G | GTGTGTGT others(3): Show |
30 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(27): Show | 31 | HG00099.hp1 HG00140.hp1 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.114-25486_114-2548 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667503 | ||||||
| chr6:129667503
|
G | GTGTGTGT others(5): Show |
29 | a0001c0001t0001g0106a0001c0001t0001g0126a0001c0001t0001g0166others(26): Show | 29 | HG00408.hp2 HG00741.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.114-25486_114-2548 others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667503 | ||||||
| chr6:129667503
|
G | GTGTGTGT others(7): Show |
7 | a0001c0001t0001g0094a0001c0001t0001g0108a0001c0001t0001g0216others(4): Show | 7 | HG00140.hp2 HG00741.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.114-25486_114-2548 others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667503 | ||||||
| chr6:129667536
|
C | A | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.114-25518G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667536 | ||||||
| chr6:129667747
|
G | C | 136 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(133): Show | 137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.114-25729C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667747 | ||||||
| chr6:129667905
|
G | T | 9 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(6): Show | 9 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.114-25887C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129667905 | ||||||
| chr6:129668188
|
C | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.114-26170G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668188 | ||||||
| chr6:129668287
|
T | C | 3 | a0001c0011t0001g0056a0002c0002t0001g0006a0003c0004t0001g0151 | 3 | HG03098.hp2 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-26269A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668287 | ||||||
| chr6:129668362
|
T | TCA | 18 | a0001c0001t0001g0085a0001c0001t0001g0136a0001c0001t0001g0140others(15): Show | 18 | HG00558.hp1 HG00639.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.114-26346_114-2634 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | ||||||
| chr6:129668362
|
T | TCACA | 30 | a0001c0001t0001g0076a0001c0001t0001g0089a0001c0001t0001g0099others(27): Show | 30 | HG00438.hp1 HG00639.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.114-26348_114-2634 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | ||||||
| chr6:129668362
|
T | TCACACA | 32 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0124others(29): Show | 32 | HG00558.hp2 HG00621.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.114-26350_114-2634 others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | ||||||
| chr6:129668362
|
T | TCACACAC others(1): Show |
16 | a0001c0001t0001g0074a0001c0001t0001g0080a0001c0001t0001g0127others(13): Show | 16 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.114-26352_114-2634 others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | ||||||
| chr6:129668362
|
T | TCACACAC others(3): Show |
8 | a0001c0001t0001g0086a0001c0001t0001g0193a0001c0001t0001g0201others(5): Show | 8 | HG00408.hp1 HG02027.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.114-26354_114-2634 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | ||||||
| chr6:129668362
|
T | TCACACAC others(7): Show |
3 | a0001c0001t0002g0172a0002c0002t0002g0019a0002c0002t0002g0020 | 3 | HG01261.hp2 HG02273.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.114-26345_114-2634 others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | ||||||
| chr6:129668362
|
T | TCACACAC others(11): Show |
1 | a0002c0002t0002g0050 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.114-26345_114-2634 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | ||||||
| chr6:129668362
|
T | TCACACAC others(5): Show |
2 | a0001c0001t0001g0130a0001c0001t0001g0146 | 2 | HG02523.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.114-26356_114-2634 others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | ||||||
| chr6:129668362
|
T | TCACACAC others(7): Show |
3 | a0001c0001t0001g0144a0001c0001t0002g0145a0003c0004t0005g0088 | 3 | HG02280.hp2 HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.114-26358_114-2634 others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | ||||||
| chr6:129668362
|
TCA | T | 25 | a0001c0001t0001g0091a0001c0001t0001g0132a0001c0001t0001g0135others(22): Show | 25 | HG00408.hp2 HG00597.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.114-26346_114-2634 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | ||||||
| chr6:129668362
|
TCACA | T | 5 | a0001c0001t0001g0079a0001c0001t0001g0216a0001c0001t0007g0077others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.114-26348_114-2634 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668362 | ||||||
| chr6:129668377
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.114-26359G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668377 | ||||||
| chr6:129668378
|
A | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(57): Show | 61 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.114-26360T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668378 | ||||||
| chr6:129668391
|
CACACACA others(3): Show |
C | 5 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0002g0143others(2): Show | 5 | HG00099.hp2 HG01074.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-26383_114-2637 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668391 | ||||||
| chr6:129668393
|
CACACACA others(1): Show |
C | 3 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065 | 3 | HG01433.hp1 HG02004.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.114-26383_114-2637 others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668393 | ||||||
| chr6:129668395
|
CACACAG | C | 3 | a0001c0001t0001g0195a0002c0002t0001g0016a0002c0002t0001g0017 | 3 | HG01175.hp2 HG01261.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.114-26383_114-2637 others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668395 | ||||||
| chr6:129668401
|
G | C | 38 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(35): Show | 38 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.114-26383C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668401 | ||||||
| chr6:129668403
|
C | G | 1 | a0001c0001t0005g0212 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.114-26385G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668403 | ||||||
| chr6:129668427
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.114-26409T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668427 | ||||||
| chr6:129668481
|
A | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(116): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.114-26463T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668481 | ||||||
| chr6:129668687
|
G | A | 12 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(9): Show | 12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-26669C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668687 | ||||||
| chr6:129668784
|
C | G | 3 | a0001c0001t0001g0079a0001c0001t0007g0077a0001c0001t0007g0078 | 3 | HG02896.hp1 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.114-26766G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668784 | ||||||
| chr6:129668828
|
C | T | 15 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0084others(12): Show | 15 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.114-26810G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129668828 | ||||||
| chr6:129669132
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.114-27114A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669132 | ||||||
| chr6:129669172
|
C | CTT | 33 | a0001c0001t0001g0132a0001c0001t0001g0135a0001c0001t0001g0186others(30): Show | 33 | HG00408.hp2 HG00597.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.114-27156_114-2715 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669172 | ||||||
| chr6:129669172
|
C | T | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.114-27154G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669172 | ||||||
| chr6:129669208
|
C | G | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.114-27190G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669208 | ||||||
| chr6:129669233
|
G | C | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.114-27215C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669233 | ||||||
| chr6:129669526
|
C | T | 5 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0004g0123others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-27508G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669526 | ||||||
| chr6:129669548
|
G | A | 58 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(55): Show | 59 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.114-27530C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669548 | ||||||
| chr6:129669603
|
C | G | 1 | a0002c0002t0001g0014 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.114-27585G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669603 | ||||||
| chr6:129669692
|
G | A | 8 | a0001c0001t0001g0108a0001c0001t0001g0179a0001c0001t0001g0204others(5): Show | 8 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-27674C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669692 | ||||||
| chr6:129669782
|
C | CA | 12 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(9): Show | 12 | HG00099.hp2 HG01074.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-27765dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669782 | ||||||
| chr6:129669782
|
CA | C | 36 | a0001c0001t0001g0079a0001c0001t0001g0132a0001c0001t0001g0135others(33): Show | 36 | HG00408.hp2 HG00597.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.114-27765delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669782 | ||||||
| chr6:129669795
|
A | T | 1 | a0001c0001t0001g0121 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.114-27777T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129669795 | ||||||
| chr6:129670114
|
A | C | 3 | a0001c0011t0001g0056a0002c0002t0001g0006a0003c0004t0001g0151 | 3 | HG03098.hp2 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-28096T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670114 | ||||||
| chr6:129670118
|
C | G | 3 | a0001c0001t0001g0177a0001c0001t0001g0201a0001c0001t0001g0213 | 3 | HG01358.hp2 HG01928.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.114-28100G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670118 | ||||||
| chr6:129670221
|
C | T | 1 | a0001c0001t0015g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.114-28203G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670221 | ||||||
| chr6:129670586
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.114-28568G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670586 | ||||||
| chr6:129670636
|
G | A | 8 | a0001c0001t0002g0068a0001c0001t0002g0171a0001c0001t0002g0184others(5): Show | 8 | HG00438.hp1 HG02056.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.114-28618C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670636 | ||||||
| chr6:129670688
|
C | CT | 6 | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0127others(3): Show | 6 | HG01175.hp1 HG02056.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.114-28671dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670688 | ||||||
| chr6:129670688
|
CT | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(101): Show | 105 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.114-28671delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670688 | ||||||
| chr6:129670688
|
CTT | C | 34 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(31): Show | 34 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(31): Show |
intron_variant | MODIFIER | c.114-28672_114-2867 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670688 | ||||||
| chr6:129670725
|
A | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.114-28707T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670725 | ||||||
| chr6:129670990
|
A | T | 12 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(9): Show | 12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-28972T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129670990 | ||||||
| chr6:129671332
|
A | G | 1 | a0002c0002t0018g0009 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.114-29314T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129671332 | ||||||
| chr6:129671424
|
C | A | 23 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(20): Show | 23 | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.114-29406G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129671424 | ||||||
| chr6:129671425
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.114-29407C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129671425 | ||||||
| chr6:129671591
|
T | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(83): Show | 87 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(84): Show |
intron_variant | MODIFIER | c.114-29573A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129671591 | ||||||
| chr6:129671599
|
C | T | 12 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(9): Show | 12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-29581G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129671599 | ||||||
| chr6:129671807
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0127 | 2 | HG01175.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.114-29789G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129671807 | ||||||
| chr6:129672017
|
C | T | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 8 | HG00099.hp2 HG01074.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-29999G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672017 | ||||||
| chr6:129672054
|
G | T | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.114-30036C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672054 | ||||||
| chr6:129672089
|
G | A | 55 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(52): Show | 55 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.114-30071C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672089 | ||||||
| chr6:129672097
|
G | A | 12 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(9): Show | 12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.114-30079C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672097 | ||||||
| chr6:129672109
|
G | A | 5 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0004g0123others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-30091C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672109 | ||||||
| chr6:129672172
|
G | A | 5 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0004g0123others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-30154C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672172 | ||||||
| chr6:129672188
|
C | T | 2 | a0001c0001t0002g0057a0001c0001t0002g0173 | 2 | HG02818.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.114-30170G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672188 | ||||||
| chr6:129672219
|
G | A | 1 | a0001c0001t0001g0214 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.114-30201C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672219 | ||||||
| chr6:129672378
|
G | A | 3 | a0001c0011t0001g0056a0002c0002t0001g0006a0003c0004t0001g0151 | 3 | HG03098.hp2 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-30360C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672378 | ||||||
| chr6:129672555
|
A | C | 35 | a0001c0001t0001g0132a0001c0001t0001g0135a0001c0001t0001g0186others(32): Show | 35 | HG00408.hp2 HG00597.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.114-30537T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672555 | ||||||
| chr6:129672656
|
C | A | 8 | a0001c0001t0001g0108a0001c0001t0001g0179a0001c0001t0001g0204others(5): Show | 8 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.114-30638G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672656 | ||||||
| chr6:129672750
|
G | T | 7 | a0001c0001t0001g0108a0001c0001t0001g0179a0001c0001t0001g0204others(4): Show | 7 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.114-30732C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129672750 | ||||||
| chr6:129673129
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.114-31111A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673129 | ||||||
| chr6:129673222
|
C | T | 5 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0004g0123others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-31204G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673222 | ||||||
| chr6:129673223
|
G | A | 3 | a0001c0011t0001g0056a0002c0002t0001g0006a0003c0004t0001g0151 | 3 | HG03098.hp2 HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.114-31205C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673223 | ||||||
| chr6:129673353
|
C | CA | 5 | a0001c0001t0001g0084a0001c0001t0019g0233a0001c0003t0002g0211others(2): Show | 5 | HG00621.hp2 HG03669.hp2 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-31336dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673353 | ||||||
| chr6:129673353
|
C | CAA | 13 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(10): Show | 13 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.114-31337_114-3133 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673353 | ||||||
| chr6:129673429
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.114-31411C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673429 | ||||||
| chr6:129673438
|
C | G | 1 | a0002c0002t0001g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.114-31420G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673438 | ||||||
| chr6:129673510
|
C | T | 74 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(71): Show | 75 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.114-31492G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673510 | ||||||
| chr6:129673667
|
T | C | 5 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0004g0123others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-31649A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673667 | ||||||
| chr6:129673701
|
G | T | 1 | a0002c0002t0001g0008 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.114-31683C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673701 | ||||||
| chr6:129673795
|
T | C | 5 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0004g0123others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-31777A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673795 | ||||||
| chr6:129673910
|
T | C | 1 | a0002c0002t0001g0015 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.114-31892A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129673910 | ||||||
| chr6:129674267
|
G | T | 1 | a0001c0001t0015g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.114-32249C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129674267 | ||||||
| chr6:129674398
|
A | T | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.114-32380T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129674398 | ||||||
| chr6:129674468
|
C | T | 9 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(6): Show | 9 | HG00099.hp2 HG01074.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.114-32450G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129674468 | ||||||
| chr6:129674679
|
A | G | 2 | a0001c0001t0001g0090a0001c0001t0001g0101 | 2 | HG01361.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.114-32661T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129674679 | ||||||
| chr6:129674865
|
C | T | 1 | a0001c0001t0002g0087 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.114-32847G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129674865 | ||||||
| chr6:129674880
|
T | C | 81 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(78): Show | 81 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.114-32862A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129674880 | ||||||
| chr6:129674901
|
T | G | 1 | a0001c0001t0003g0224 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.114-32883A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129674901 | ||||||
| chr6:129674932
|
C | T | 4 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.114-32914G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129674932 | ||||||
| chr6:129675057
|
C | T | 1 | a0001c0001t0001g0155 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.114-33039G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129675057 | ||||||
| chr6:129675157
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.114-33139G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129675157 | ||||||
| chr6:129675371
|
G | A | 5 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0004g0123others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.114-33353C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129675371 | ||||||
| chr6:129675383
|
C | CA | 10 | a0001c0001t0001g0090a0001c0001t0001g0107a0001c0001t0001g0108others(7): Show | 10 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.114-33366dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129675383 | ||||||
| chr6:129675383
|
CA | C | 42 | a0001c0001t0001g0132a0001c0001t0001g0135a0001c0001t0001g0144others(39): Show | 42 | HG00408.hp2 HG00597.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.114-33366delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129675383 | ||||||
| chr6:129675537
|
C | A | 24 | a0001c0001t0001g0067a0001c0001t0001g0079a0001c0001t0001g0084others(21): Show | 24 | HG00423.hp1 HG02280.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.114-33519G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129675537 | ||||||
| chr6:129675634
|
CCTG | C | 3 | a0001c0001t0001g0129a0001c0001t0001g0150a0001c0001t0001g0154 | 3 | HG00558.hp2 NA18942.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.114-33619_114-3361 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129675634 | ||||||
| chr6:129675764
|
G | C | 1 | a0003c0004t0001g0151 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.114-33746C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129675764 | ||||||
| chr6:129675919
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.114-33901C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129675919 | ||||||
| chr6:129676370
|
A | G | 79 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(76): Show | 80 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(77): Show |
intron_variant | MODIFIER | c.113+33654T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676370 | ||||||
| chr6:129676371
|
T | A | 1 | a0001c0001t0001g0191 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.113+33653A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676371 | ||||||
| chr6:129676740
|
C | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.113+33284G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676740 | ||||||
| chr6:129676912
|
CCTCT | C | 4 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.113+33108_113+3311 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676912 | ||||||
| chr6:129676912
|
CCTCTTTT others(1): Show |
C | 27 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(24): Show | 28 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.113+33104_113+3311 others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676912 | ||||||
| chr6:129676912
|
CCTCTTTT others(2): Show |
C | 26 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0001t0001g0103others(23): Show | 26 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.113+33103_113+3311 others(13): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676912 | ||||||
| chr6:129676912
|
CCTCTTTT others(3): Show |
C | 4 | a0001c0001t0001g0164a0001c0001t0019g0233a0002c0002t0001g0052others(1): Show | 4 | HG02622.hp2 NA18969.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.113+33102_113+3311 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676912 | ||||||
| chr6:129676912
|
CCTCTTTT others(4): Show |
C | 5 | a0001c0001t0001g0108a0001c0001t0001g0179a0001c0001t0001g0204others(2): Show | 5 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+33101_113+3311 others(15): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676912 | ||||||
| chr6:129676912
|
CCTCTTTT others(9): Show |
C | 1 | a0001c0001t0003g0128 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.113+33096_113+3311 others(20): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676912 | ||||||
| chr6:129676912
|
CCTCTTTT others(13): Show |
C | 9 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(6): Show | 9 | HG00099.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.113+33092_113+3311 others(24): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676912 | ||||||
| chr6:129676915
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0015g0110 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.113+33099_113+3310 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | ||||||
| chr6:129676915
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0091 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.113+33098_113+3310 others(15): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | ||||||
| chr6:129676915
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0001g0140a0001c0001t0004g0139a0001c0001t0010g0137 | 3 | HG02965.hp2 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.113+33096_113+3310 others(17): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | ||||||
| chr6:129676915
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0003g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.113+33095_113+3310 others(18): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | ||||||
| chr6:129676915
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0002g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.113+33091_113+3310 others(22): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | ||||||
| chr6:129676915
|
C | CTTTTTTT others(16): Show |
1 | a0001c0001t0001g0136 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.113+33086_113+3310 others(27): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | ||||||
| chr6:129676915
|
CT | C | 39 | a0001c0001t0001g0076a0001c0001t0001g0085a0001c0001t0001g0089others(36): Show | 39 | HG00544.hp1 HG00639.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.113+33108delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | ||||||
| chr6:129676915
|
CTT | C | 40 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0083others(37): Show | 40 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.113+33107_113+3310 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | ||||||
| chr6:129676915
|
CTTTTTT | C | 30 | a0001c0001t0001g0132a0001c0001t0001g0206a0001c0001t0001g0209others(27): Show | 30 | HG00408.hp2 HG00597.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.113+33103_113+3310 others(10): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | ||||||
| chr6:129676915
|
CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0003g0075a0001c0001t0003g0225a0001c0001t0011g0141others(1): Show | 4 | HG02615.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+33096_113+3310 others(17): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | ||||||
| chr6:129676915
|
CTTTTTTT others(13): Show |
C | 5 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0004g0123others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+33089_113+3310 others(24): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676915 | ||||||
| chr6:129676948
|
T | A | 79 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(76): Show | 80 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(77): Show |
intron_variant | MODIFIER | c.113+33076A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676948 | ||||||
| chr6:129676950
|
A | G | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+33074T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129676950 | ||||||
| chr6:129677103
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.113+32921G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677103 | ||||||
| chr6:129677122
|
G | A | 7 | a0001c0001t0001g0108a0001c0001t0001g0179a0001c0001t0001g0204others(4): Show | 7 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.113+32902C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677122 | ||||||
| chr6:129677134
|
T | C | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+32890A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677134 | ||||||
| chr6:129677351
|
C | T | 2 | a0001c0001t0003g0128a0001c0001t0003g0133 | 2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.113+32673G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677351 | ||||||
| chr6:129677361
|
C | T | 8 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 8 | HG00099.hp2 HG01074.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.113+32663G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677361 | ||||||
| chr6:129677392
|
CA | C | 44 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0001g0084others(41): Show | 44 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.113+32631delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677392 | ||||||
| chr6:129677407
|
A | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(62): Show | 66 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(63): Show |
intron_variant | MODIFIER | c.113+32617T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677407 | ||||||
| chr6:129677511
|
A | G | 1 | a0006c0010t0001g0197 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.113+32513T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677511 | ||||||
| chr6:129677530
|
A | G | 3 | a0001c0001t0001g0177a0001c0001t0001g0201a0001c0001t0001g0213 | 3 | HG01358.hp2 HG01928.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.113+32494T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677530 | ||||||
| chr6:129677934
|
A | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(53): Show | 57 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.113+32090T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129677934 | ||||||
| chr6:129678125
|
G | C | 137 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(134): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.113+31899C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129678125 | ||||||
| chr6:129678311
|
G | A | 1 | a0001c0001t0003g0226 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.113+31713C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129678311 | ||||||
| chr6:129678400
|
T | C | 12 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0231others(9): Show | 12 | HG00597.hp2 HG00741.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.113+31624A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129678400 | ||||||
| chr6:129678412
|
AACGGATG others(15): Show |
A | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+31590_113+3161 others(26): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129678412 | ||||||
| chr6:129678981
|
C | G | 7 | a0001c0001t0001g0108a0001c0001t0001g0179a0001c0001t0001g0204others(4): Show | 7 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.113+31043G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129678981 | ||||||
| chr6:129679083
|
T | C | 58 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(55): Show | 59 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.113+30941A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129679083 | ||||||
| chr6:129679170
|
TACTA | T | 10 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0082others(7): Show | 10 | HG00597.hp2 HG03669.hp2 HG04115.hp2 others(7): Show |
intron_variant | MODIFIER | c.113+30850_113+3085 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129679170 | ||||||
| chr6:129679356
|
G | T | 1 | a0001c0001t0001g0131 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.113+30668C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129679356 | ||||||
| chr6:129679902
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.113+30122C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129679902 | ||||||
| chr6:129679991
|
C | T | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+30033G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129679991 | ||||||
| chr6:129680162
|
C | G | 2 | a0001c0001t0008g0118a0001c0001t0008g0228 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.113+29862G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680162 | ||||||
| chr6:129680168
|
T | C | 12 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(9): Show | 12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.113+29856A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680168 | ||||||
| chr6:129680218
|
A | G | 1 | a0001c0001t0001g0214 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.113+29806T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680218 | ||||||
| chr6:129680242
|
G | T | 2 | a0001c0011t0001g0056a0003c0004t0001g0151 | 2 | HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.113+29782C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680242 | ||||||
| chr6:129680348
|
C | T | 1 | a0002c0002t0003g0022 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.113+29676G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680348 | ||||||
| chr6:129680428
|
T | C | 14 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(11): Show | 14 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.113+29596A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680428 | ||||||
| chr6:129680503
|
C | T | 3 | a0001c0001t0001g0079a0001c0001t0007g0077a0001c0001t0007g0078 | 3 | HG02896.hp1 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.113+29521G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680503 | ||||||
| chr6:129680665
|
C | T | 14 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(11): Show | 14 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.113+29359G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680665 | ||||||
| chr6:129680699
|
C | G | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.113+29325G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680699 | ||||||
| chr6:129680732
|
A | G | 6 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(3): Show | 6 | HG02895.hp1 HG02897.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.113+29292T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680732 | ||||||
| chr6:129680992
|
G | A | 12 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(9): Show | 12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.113+29032C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129680992 | ||||||
| chr6:129681067
|
A | C | 1 | a0001c0001t0001g0166 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.113+28957T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129681067 | ||||||
| chr6:129681077
|
G | A | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+28947C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129681077 | ||||||
| chr6:129681327
|
C | T | 1 | a0001c0001t0002g0181 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.113+28697G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129681327 | ||||||
| chr6:129681335
|
C | T | 2 | a0001c0001t0001g0144a0001c0001t0002g0145 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.113+28689G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129681335 | ||||||
| chr6:129681398
|
A | G | 12 | a0001c0001t0001g0067a0001c0001t0001g0084a0001c0001t0001g0091others(9): Show | 12 | HG00423.hp1 HG02486.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.113+28626T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129681398 | ||||||
| chr6:129681457
|
A | T | 2 | a0001c0001t0008g0118a0001c0001t0008g0228 | 2 | HG02922.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.113+28567T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129681457 | ||||||
| chr6:129681877
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.113+28147C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129681877 | ||||||
| chr6:129682428
|
C | T | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.113+27596G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129682428 | ||||||
| chr6:129682436
|
T | C | 5 | a0001c0001t0002g0172a0002c0002t0002g0019a0002c0002t0002g0020others(2): Show | 5 | HG01261.hp2 HG01952.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+27588A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129682436 | ||||||
| chr6:129682470
|
CT | C | 3 | a0001c0001t0019g0233a0001c0011t0001g0056a0003c0004t0001g0151 | 3 | HG03098.hp2 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.113+27553delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129682470 | ||||||
| chr6:129682476
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.113+27548G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129682476 | ||||||
| chr6:129682922
|
T | C | 4 | a0001c0001t0001g0142a0001c0001t0003g0058a0001c0001t0003g0059others(1): Show | 4 | HG02895.hp1 HG02897.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.113+27102A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129682922 | ||||||
| chr6:129683050
|
TTTTTC | T | 6 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(3): Show | 6 | HG01433.hp1 HG01928.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+26969_113+2697 others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683050 | ||||||
| chr6:129683055
|
CT | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(97): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.113+26968delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683055 | ||||||
| chr6:129683055
|
CTT | C | 5 | a0001c0001t0001g0131a0001c0001t0003g0128a0001c0001t0003g0133others(2): Show | 5 | HG02970.hp2 HG03098.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+26967_113+2696 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683055 | ||||||
| chr6:129683056
|
T | C | 6 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(3): Show | 6 | HG01433.hp1 HG01928.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+26968A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683056 | ||||||
| chr6:129683069
|
G | T | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+26955C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683069 | ||||||
| chr6:129683075
|
T | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(115): Show | 119 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.113+26949A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683075 | ||||||
| chr6:129683173
|
A | T | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.113+26851T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683173 | ||||||
| chr6:129683232
|
C | T | 43 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(40): Show | 43 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.113+26792G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683232 | ||||||
| chr6:129683340
|
G | T | 1 | a0001c0003t0002g0190 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.113+26684C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683340 | ||||||
| chr6:129683454
|
C | T | 44 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(41): Show | 44 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.113+26570G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683454 | ||||||
| chr6:129683658
|
G | T | 1 | a0001c0001t0001g0153 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.113+26366C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683658 | ||||||
| chr6:129683839
|
G | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(65): Show | 69 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.113+26185C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683839 | ||||||
| chr6:129683866
|
C | T | 41 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(38): Show | 41 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.113+26158G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129683866 | ||||||
| chr6:129684204
|
G | A | 1 | a0001c0001t0002g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.113+25820C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129684204 | ||||||
| chr6:129684373
|
T | C | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.113+25651A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129684373 | ||||||
| chr6:129684513
|
T | C | 1 | a0001c0001t0004g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.113+25511A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129684513 | ||||||
| chr6:129684522
|
G | T | 85 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0079others(82): Show | 85 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.113+25502C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129684522 | ||||||
| chr6:129684571
|
T | G | 41 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(38): Show | 41 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.113+25453A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129684571 | ||||||
| chr6:129684602
|
C | T | 2 | a0002c0002t0003g0022a0002c0002t0003g0023 | 2 | HG00558.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.113+25422G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129684602 | ||||||
| chr6:129684603
|
G | A | 5 | a0001c0001t0001g0079a0001c0001t0001g0144a0001c0001t0002g0145others(2): Show | 5 | HG02280.hp2 HG02451.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+25421C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129684603 | ||||||
| chr6:129684845
|
T | C | 1 | a0002c0002t0002g0013 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.113+25179A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129684845 | ||||||
| chr6:129685092
|
G | T | 12 | a0001c0001t0001g0177a0001c0001t0001g0201a0001c0001t0001g0209others(9): Show | 12 | HG00597.hp2 HG00741.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.113+24932C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685092 | ||||||
| chr6:129685173
|
T | G | 3 | a0001c0001t0001g0131a0001c0001t0003g0128a0001c0001t0003g0133 | 3 | HG02970.hp2 HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.113+24851A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685173 | ||||||
| chr6:129685237
|
T | G | 20 | a0001c0001t0001g0206a0001c0001t0001g0214a0001c0001t0001g0215others(17): Show | 20 | HG00408.hp2 HG00544.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.113+24787A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685237 | ||||||
| chr6:129685282
|
G | A | 41 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(38): Show | 41 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.113+24742C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685282 | ||||||
| chr6:129685352
|
C | A | 1 | a0001c0001t0002g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.113+24672G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685352 | ||||||
| chr6:129685374
|
G | GCAGGCAC others(5): Show |
39 | a0001c0001t0001g0131a0001c0001t0001g0135a0001c0001t0001g0177others(36): Show | 39 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.113+24638_113+2464 others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685374 | ||||||
| chr6:129685570
|
C | T | 140 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(137): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.113+24454G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685570 | ||||||
| chr6:129685584
|
T | C | 1 | a0003c0004t0005g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.113+24440A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685584 | ||||||
| chr6:129685602
|
G | GGTTA | 44 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(41): Show | 44 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.113+24418_113+2442 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685602 | ||||||
| chr6:129685725
|
T | G | 173 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(170): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.113+24299A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685725 | ||||||
| chr6:129685750
|
CT | C | 41 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(38): Show | 41 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.113+24273delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685750 | ||||||
| chr6:129685839
|
G | A | 5 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0002g0066others(2): Show | 6 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+24185C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129685839 | ||||||
| chr6:129686079
|
T | A | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.113+23945A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686079 | ||||||
| chr6:129686108
|
G | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0064others(94): Show | 98 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.113+23916C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686108 | ||||||
| chr6:129686239
|
CCACGCTC others(5): Show |
C | 20 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(17): Show | 21 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.113+23773_113+2378 others(16): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686239 | ||||||
| chr6:129686271
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.113+23753G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686271 | ||||||
| chr6:129686289
|
T | A | 33 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0001t0001g0132others(30): Show | 33 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.113+23735A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686289 | ||||||
| chr6:129686332
|
T | C | 97 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0064others(94): Show | 98 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.113+23692A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686332 | ||||||
| chr6:129686452
|
C | A | 34 | a0001c0001t0001g0135a0001c0001t0001g0201a0001c0001t0001g0206others(31): Show | 34 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.113+23572G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686452 | ||||||
| chr6:129686619
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.113+23405T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686619 | ||||||
| chr6:129686788
|
C | CT | 38 | a0001c0001t0001g0001a0001c0001t0001g0080a0001c0001t0001g0096others(35): Show | 39 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(36): Show |
intron_variant | MODIFIER | c.113+23235dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686788 | ||||||
| chr6:129686788
|
CT | C | 8 | a0001c0001t0001g0150a0001c0001t0002g0117a0001c0001t0002g0167others(5): Show | 8 | HG02004.hp1 HG02970.hp1 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.113+23235delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686788 | ||||||
| chr6:129686788
|
CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(4): Show | 7 | HG01433.hp1 HG01928.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.113+23226_113+2323 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686788 | ||||||
| chr6:129686839
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.113+23185C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686839 | ||||||
| chr6:129686859
|
C | T | 2 | a0002c0002t0001g0021a0002c0002t0001g0051 | 2 | NA18977.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.113+23165G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686859 | ||||||
| chr6:129686893
|
C | T | 3 | a0001c0001t0001g0144a0001c0001t0002g0145a0007c0008t0004g0055 | 3 | HG02280.hp2 HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.113+23131G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686893 | ||||||
| chr6:129686949
|
C | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.113+23075G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686949 | ||||||
| chr6:129686973
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0064others(91): Show | 95 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.113+23051A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686973 | ||||||
| chr6:129686974
|
TTTTC | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0072a0001c0001t0001g0073others(22): Show | 26 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.113+23046_113+2304 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686974 | ||||||
| chr6:129686975
|
TTTC | T | 11 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(8): Show | 11 | HG01433.hp1 HG01928.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.113+23046_113+2304 others(7): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686975 | ||||||
| chr6:129686977
|
TC | T | 23 | a0001c0001t0001g0096a0001c0001t0001g0146a0001c0001t0001g0178others(20): Show | 23 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.113+23046delG | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686977 | ||||||
| chr6:129686978
|
C | CT | 37 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0001g0098others(34): Show | 37 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.113+23045dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686978 | ||||||
| chr6:129686978
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.113+23046G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686978 | ||||||
| chr6:129686978
|
CTTTT | C | 34 | a0001c0001t0001g0135a0001c0001t0001g0201a0001c0001t0001g0206others(31): Show | 34 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.113+23042_113+2304 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686978 | ||||||
| chr6:129686978
|
CTTTTTTT others(1): Show |
C | 41 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(38): Show | 41 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.113+23038_113+2304 others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686978 | ||||||
| chr6:129686978
|
CTTTTTTT others(4): Show |
C | 2 | a0002c0002t0001g0016a0002c0002t0001g0017 | 2 | HG01175.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.113+23035_113+2304 others(15): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129686978 | ||||||
| chr6:129687069
|
A | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0064others(93): Show | 97 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.113+22955T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687069 | ||||||
| chr6:129687146
|
C | T | 1 | a0001c0001t0004g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.113+22878G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687146 | ||||||
| chr6:129687173
|
G | A | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+22851C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687173 | ||||||
| chr6:129687273
|
C | T | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+22751G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687273 | ||||||
| chr6:129687297
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.113+22727A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687297 | ||||||
| chr6:129687300
|
A | C | 46 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(43): Show | 46 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.113+22724T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687300 | ||||||
| chr6:129687383
|
T | C | 1 | a0001c0001t0002g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.113+22641A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687383 | ||||||
| chr6:129687398
|
G | A | 32 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0001t0001g0148others(29): Show | 32 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.113+22626C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687398 | ||||||
| chr6:129687430
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.113+22594T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687430 | ||||||
| chr6:129687735
|
C | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(20): Show | 24 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.113+22289G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687735 | ||||||
| chr6:129687758
|
G | T | 41 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(38): Show | 41 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.113+22266C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687758 | ||||||
| chr6:129687787
|
A | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0064others(93): Show | 97 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.113+22237T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687787 | ||||||
| chr6:129687789
|
A | AT | 95 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0064others(92): Show | 96 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.113+22234dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687789 | ||||||
| chr6:129687789
|
AT | A | 41 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(38): Show | 41 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.113+22234delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687789 | ||||||
| chr6:129687965
|
A | G | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+22059T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129687965 | ||||||
| chr6:129688167
|
C | A | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.113+21857G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688167 | ||||||
| chr6:129688359
|
G | GTT | 96 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0064others(93): Show | 97 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.113+21664_113+2166 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688359 | ||||||
| chr6:129688522
|
G | A | 24 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(21): Show | 25 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.113+21502C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688522 | ||||||
| chr6:129688545
|
C | A | 26 | a0001c0001t0001g0096a0001c0001t0001g0146a0001c0001t0001g0178others(23): Show | 26 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.113+21479G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688545 | ||||||
| chr6:129688593
|
G | T | 1 | a0001c0001t0003g0205 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.113+21431C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688593 | ||||||
| chr6:129688652
|
C | A | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+21372G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688652 | ||||||
| chr6:129688689
|
G | A | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.113+21335C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688689 | ||||||
| chr6:129688753
|
T | C | 2 | a0001c0001t0001g0089a0001c0001t0001g0090 | 2 | HG01099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.113+21271A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688753 | ||||||
| chr6:129688792
|
C | CA | 112 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(109): Show | 113 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.113+21231dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688792 | ||||||
| chr6:129688803
|
A | AT | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG00741.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.113+21220_113+2122 others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688803 | ||||||
| chr6:129688965
|
C | T | 2 | a0001c0001t0006g0198a0006c0010t0001g0197 | 2 | HG03704.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.113+21059G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688965 | ||||||
| chr6:129688996
|
G | C | 21 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(18): Show | 22 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.113+21028C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129688996 | ||||||
| chr6:129689031
|
C | T | 1 | a0002c0002t0002g0019 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.113+20993G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129689031 | ||||||
| chr6:129689136
|
C | A | 1 | a0002c0002t0001g0040 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.113+20888G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129689136 | ||||||
| chr6:129689227
|
T | C | 139 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.113+20797A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129689227 | ||||||
| chr6:129689354
|
C | T | 2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+20670G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129689354 | ||||||
| chr6:129689440
|
G | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0064others(93): Show | 97 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.113+20584C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129689440 | ||||||
| chr6:129689454
|
G | A | 1 | a0004c0013t0001g0208 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.113+20570C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129689454 | ||||||
| chr6:129689994
|
C | T | 31 | a0001c0001t0001g0094a0001c0001t0001g0148a0001c0001t0001g0150others(28): Show | 31 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.113+20030G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129689994 | ||||||
| chr6:129689997
|
C | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(175): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.113+20027G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129689997 | ||||||
| chr6:129690059
|
CCAAA | C | 4 | a0001c0001t0002g0172a0002c0002t0002g0019a0002c0002t0002g0020others(1): Show | 4 | HG01261.hp2 HG01952.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+19961_113+1996 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129690059 | ||||||
| chr6:129690124
|
C | CGT | 24 | a0001c0001t0001g0096a0001c0001t0001g0146a0001c0001t0001g0178others(21): Show | 24 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.113+19898_113+1989 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129690124 | ||||||
| chr6:129690124
|
C | CGTGT | 34 | a0001c0001t0001g0135a0001c0001t0001g0201a0001c0001t0001g0206others(31): Show | 34 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.113+19896_113+1989 others(8): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129690124 | ||||||
| chr6:129690521
|
A | G | 45 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(42): Show | 45 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.113+19503T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129690521 | ||||||
| chr6:129690753
|
T | C | 1 | a0001c0001t0003g0237 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.113+19271A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129690753 | ||||||
| chr6:129690774
|
T | C | 73 | a0001c0001t0001g0001a0001c0001t0001g0063a0001c0001t0001g0064others(70): Show | 74 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.113+19250A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129690774 | ||||||
| chr6:129690908
|
G | A | 37 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0135others(34): Show | 37 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.113+19116C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129690908 | ||||||
| chr6:129690980
|
C | T | 1 | a0001c0001t0002g0082 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.113+19044G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129690980 | ||||||
| chr6:129691051
|
C | A | 1 | a0002c0002t0001g0006 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.113+18973G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691051 | ||||||
| chr6:129691080
|
C | T | 24 | a0001c0001t0001g0096a0001c0001t0001g0146a0001c0001t0001g0178others(21): Show | 24 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.113+18944G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691080 | ||||||
| chr6:129691125
|
A | G | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0108 | 3 | HG00140.hp2 HG01099.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.113+18899T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691125 | ||||||
| chr6:129691213
|
A | T | 6 | a0001c0001t0001g0100a0001c0001t0001g0105a0001c0001t0001g0106others(3): Show | 6 | NA18950.hp1 NA18983.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.113+18811T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691213 | ||||||
| chr6:129691228
|
C | T | 32 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(29): Show | 32 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.113+18796G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691228 | ||||||
| chr6:129691500
|
C | T | 41 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(38): Show | 41 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.113+18524G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691500 | ||||||
| chr6:129691698
|
C | T | 1 | a0002c0002t0001g0014 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.113+18326G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691698 | ||||||
| chr6:129691876
|
G | A | 1 | a0002c0002t0001g0018 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.113+18148C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691876 | ||||||
| chr6:129691904
|
C | T | 2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+18120G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691904 | ||||||
| chr6:129691924
|
A | G | 3 | a0001c0001t0001g0079a0001c0001t0007g0077a0001c0001t0007g0078 | 3 | HG02896.hp1 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.113+18100T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129691924 | ||||||
| chr6:129692010
|
C | T | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.113+18014G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129692010 | ||||||
| chr6:129692038
|
G | A | 2 | a0001c0001t0004g0134a0003c0004t0005g0088 | 2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.113+17986C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129692038 | ||||||
| chr6:129692487
|
C | A | 1 | a0001c0001t0001g0126 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.113+17537G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129692487 | ||||||
| chr6:129692699
|
C | T | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | HG00621.hp1 NA18986.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.113+17325G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129692699 | ||||||
| chr6:129692889
|
T | C | 2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+17135A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129692889 | ||||||
| chr6:129693007
|
TTTATTTT others(3): Show |
T | 2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+17007_113+1701 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693007 | ||||||
| chr6:129693039
|
C | G | 2 | a0002c0002t0001g0007a0002c0002t0001g0018 | 2 | HG00621.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.113+16985G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693039 | ||||||
| chr6:129693053
|
C | T | 2 | a0002c0002t0001g0016a0002c0002t0001g0017 | 2 | HG01175.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.113+16971G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693053 | ||||||
| chr6:129693081
|
G | A | 38 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0135others(35): Show | 38 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.113+16943C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693081 | ||||||
| chr6:129693108
|
A | G | 31 | a0001c0001t0001g0094a0001c0001t0001g0148a0001c0001t0001g0150others(28): Show | 31 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.113+16916T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693108 | ||||||
| chr6:129693355
|
G | A | 1 | a0001c0001t0013g0119 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.113+16669C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693355 | ||||||
| chr6:129693546
|
G | A | 24 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(21): Show | 25 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.113+16478C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693546 | ||||||
| chr6:129693769
|
A | AC | 43 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(40): Show | 43 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.113+16254dupG | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693769 | ||||||
| chr6:129693814
|
T | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0178 | 2 | HG00733.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.113+16210A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693814 | ||||||
| chr6:129693843
|
A | C | 7 | a0001c0001t0001g0094a0001c0001t0001g0194a0001c0001t0002g0057others(4): Show | 7 | HG02257.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.113+16181T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693843 | ||||||
| chr6:129693894
|
C | G | 1 | a0001c0001t0002g0176 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.113+16130G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693894 | ||||||
| chr6:129693908
|
CAGCTGAC others(3): Show |
C | 25 | a0001c0001t0001g0096a0001c0001t0001g0146a0001c0001t0001g0178others(22): Show | 25 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.113+16106_113+1611 others(14): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129693908 | ||||||
| chr6:129694186
|
T | G | 124 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(121): Show | 125 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.113+15838A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129694186 | ||||||
| chr6:129694264
|
G | A | 7 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(4): Show | 7 | HG01433.hp1 HG01928.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.113+15760C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129694264 | ||||||
| chr6:129694272
|
C | G | 2 | a0002c0002t0001g0015a0002c0002t0001g0049 | 2 | HG02027.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.113+15752G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129694272 | ||||||
| chr6:129694428
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.113+15596C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129694428 | ||||||
| chr6:129694564
|
T | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | HG00735.hp2 HG01106.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.113+15460A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129694564 | ||||||
| chr6:129694619
|
G | A | 33 | a0001c0001t0001g0094a0001c0001t0001g0148a0001c0001t0001g0150others(30): Show | 33 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.113+15405C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129694619 | ||||||
| chr6:129694925
|
G | C | 1 | a0001c0001t0004g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.113+15099C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129694925 | ||||||
| chr6:129694926
|
T | C | 1 | a0001c0001t0002g0081 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.113+15098A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129694926 | ||||||
| chr6:129695004
|
A | C | 50 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.113+15020T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695004 | ||||||
| chr6:129695065
|
C | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(22): Show | 26 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.113+14959G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695065 | ||||||
| chr6:129695135
|
A | C | 1 | a0001c0001t0004g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.113+14889T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695135 | ||||||
| chr6:129695263
|
A | AT | 65 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(62): Show | 66 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.113+14760dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695263 | ||||||
| chr6:129695313
|
T | C | 25 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(22): Show | 26 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.113+14711A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695313 | ||||||
| chr6:129695382
|
T | TG | 65 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(62): Show | 66 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.113+14641dupC | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695382 | ||||||
| chr6:129695553
|
G | T | 1 | a0008c0005t0003g0002 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.113+14471C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695553 | ||||||
| chr6:129695676
|
G | A | 5 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0003g0128others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+14348C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695676 | ||||||
| chr6:129695684
|
A | G | 43 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(40): Show | 43 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.113+14340T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695684 | ||||||
| chr6:129695821
|
TAAAAG | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(63): Show | 67 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.113+14198_113+1420 others(9): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695821 | ||||||
| chr6:129695904
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.113+14120G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695904 | ||||||
| chr6:129695948
|
T | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(141): Show | 145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.113+14076A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129695948 | ||||||
| chr6:129696132
|
C | T | 1 | a0001c0011t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.113+13892G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696132 | ||||||
| chr6:129696395
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.113+13629A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696395 | ||||||
| chr6:129696417
|
T | C | 65 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(62): Show | 66 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.113+13607A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696417 | ||||||
| chr6:129696514
|
G | A | 7 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(4): Show | 7 | HG01433.hp1 HG01928.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.113+13510C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696514 | ||||||
| chr6:129696639
|
C | T | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+13385G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696639 | ||||||
| chr6:129696650
|
A | G | 1 | a0001c0001t0001g0001 | 2 | HG00738.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.113+13374T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696650 | ||||||
| chr6:129696685
|
A | C | 5 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0003g0128others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+13339T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696685 | ||||||
| chr6:129696725
|
AATGCACA others(1): Show |
A | 57 | a0001c0001t0001g0096a0001c0001t0001g0135a0001c0001t0001g0146others(54): Show | 57 | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.113+13291_113+1329 others(12): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696725 | ||||||
| chr6:129696885
|
G | A | 25 | a0001c0001t0001g0096a0001c0001t0001g0146a0001c0001t0001g0178others(22): Show | 25 | HG00099.hp2 HG00544.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.113+13139C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696885 | ||||||
| chr6:129696910
|
T | G | 3 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0019g0233 | 3 | HG02280.hp2 HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.113+13114A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696910 | ||||||
| chr6:129696957
|
C | A | 2 | a0002c0002t0001g0044a0002c0002t0014g0045 | 2 | HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.113+13067G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129696957 | ||||||
| chr6:129697221
|
T | C | 5 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0003g0128others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+12803A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129697221 | ||||||
| chr6:129697242
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.113+12782G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129697242 | ||||||
| chr6:129697372
|
C | T | 3 | a0001c0001t0001g0199a0001c0001t0001g0200a0005c0012t0002g0095 | 3 | HG00099.hp2 HG01074.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.113+12652G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129697372 | ||||||
| chr6:129697442
|
AT | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(164): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.113+12581delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129697442 | ||||||
| chr6:129697442
|
ATT | A | 7 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(4): Show | 7 | HG01433.hp1 HG01928.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.113+12580_113+1258 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129697442 | ||||||
| chr6:129697455
|
T | C | 67 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(64): Show | 68 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.113+12569A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129697455 | ||||||
| chr6:129697762
|
A | G | 5 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0003g0128others(2): Show | 5 | HG02280.hp1 HG02970.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+12262T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129697762 | ||||||
| chr6:129698096
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.113+11928A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698096 | ||||||
| chr6:129698181
|
G | T | 1 | a0002c0002t0001g0014 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.113+11843C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698181 | ||||||
| chr6:129698209
|
T | C | 41 | a0001c0001t0001g0094a0001c0001t0001g0131a0001c0001t0001g0132others(38): Show | 41 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.113+11815A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698209 | ||||||
| chr6:129698471
|
T | G | 3 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0019g0233 | 3 | HG02280.hp2 HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.113+11553A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698471 | ||||||
| chr6:129698503
|
C | G | 5 | a0001c0001t0001g0099a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG00735.hp2 HG01106.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+11521G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698503 | ||||||
| chr6:129698533
|
CT | C | 83 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(80): Show | 84 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.113+11490delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698533 | ||||||
| chr6:129698533
|
CTT | C | 6 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0188others(3): Show | 6 | HG01071.hp1 HG01169.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.113+11489_113+1149 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698533 | ||||||
| chr6:129698549
|
T | G | 43 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0076others(40): Show | 43 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.113+11475A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698549 | ||||||
| chr6:129698588
|
G | A | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+11436C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698588 | ||||||
| chr6:129698605
|
A | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(64): Show | 68 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.113+11419T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698605 | ||||||
| chr6:129698691
|
G | GT | 5 | a0001c0001t0001g0136a0001c0001t0010g0137a0002c0002t0001g0012others(2): Show | 5 | HG02486.hp1 HG03195.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+11332dupA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698691 | ||||||
| chr6:129698691
|
GT | G | 139 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(136): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.113+11332delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698691 | ||||||
| chr6:129698691
|
GTT | G | 25 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(22): Show | 26 | HG00099.hp1 HG00438.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.113+11331_113+1133 others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698691 | ||||||
| chr6:129698795
|
T | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | HG00735.hp2 HG01106.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.113+11229A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698795 | ||||||
| chr6:129698831
|
T | G | 2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+11193A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698831 | ||||||
| chr6:129698841
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.113+11183G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698841 | ||||||
| chr6:129698843
|
C | T | 7 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(4): Show | 7 | HG01433.hp1 HG01928.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.113+11181G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698843 | ||||||
| chr6:129698905
|
C | T | 1 | a0001c0001t0005g0207 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.113+11119G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698905 | ||||||
| chr6:129698987
|
C | T | 2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+11037G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129698987 | ||||||
| chr6:129699110
|
T | A | 58 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0146others(55): Show | 58 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.113+10914A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699110 | ||||||
| chr6:129699127
|
C | T | 1 | a0001c0001t0002g0066 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.113+10897G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699127 | ||||||
| chr6:129699202
|
A | C | 58 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0146others(55): Show | 58 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.113+10822T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699202 | ||||||
| chr6:129699312
|
C | T | 2 | a0001c0001t0001g0096a0001c0001t0001g0178 | 2 | HG00733.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.113+10712G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699312 | ||||||
| chr6:129699593
|
G | T | 25 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(22): Show | 26 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.113+10431C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699593 | ||||||
| chr6:129699666
|
C | T | 67 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(64): Show | 68 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.113+10358G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699666 | ||||||
| chr6:129699738
|
G | C | 1 | a0001c0009t0001g0122 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.113+10286C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699738 | ||||||
| chr6:129699805
|
T | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(175): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.113+10219A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699805 | ||||||
| chr6:129699830
|
C | G | 2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+10194G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699830 | ||||||
| chr6:129699983
|
A | G | 37 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0135others(34): Show | 37 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.113+10041T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129699983 | ||||||
| chr6:129700023
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.113+10001A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129700023 | ||||||
| chr6:129700063
|
T | C | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+9961A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129700063 | ||||||
| chr6:129700120
|
G | A | 26 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0153others(23): Show | 26 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.113+9904C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129700120 | ||||||
| chr6:129700312
|
AGAT | A | 7 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(4): Show | 7 | HG01433.hp1 HG01928.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.113+9709_113+9711d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129700312 | ||||||
| chr6:129700473
|
G | A | 99 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(96): Show | 100 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.113+9551C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129700473 | ||||||
| chr6:129700936
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0019g0233 | 3 | HG02280.hp2 HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.113+9088C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129700936 | ||||||
| chr6:129700989
|
A | G | 16 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0001g0073others(13): Show | 16 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.113+9035T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129700989 | ||||||
| chr6:129700999
|
T | TA | 71 | a0001c0001t0001g0094a0001c0001t0001g0131a0001c0001t0001g0132others(68): Show | 71 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.113+9024dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129700999 | ||||||
| chr6:129701245
|
C | T | 175 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.113+8779G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129701245 | ||||||
| chr6:129701493
|
C | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(63): Show | 67 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.113+8531G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129701493 | ||||||
| chr6:129701523
|
A | G | 175 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(172): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.113+8501T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129701523 | ||||||
| chr6:129701695
|
G | A | 1 | a0003c0004t0005g0088 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.113+8329C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129701695 | ||||||
| chr6:129701773
|
T | TA | 10 | a0001c0001t0001g0136a0001c0001t0001g0140a0001c0001t0001g0142others(7): Show | 10 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.113+8250dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129701773 | ||||||
| chr6:129702068
|
A | G | 25 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(22): Show | 26 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.113+7956T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702068 | ||||||
| chr6:129702161
|
G | C | 124 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(121): Show | 125 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.113+7863C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702161 | ||||||
| chr6:129702206
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.113+7818G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702206 | ||||||
| chr6:129702364
|
C | A | 1 | a0002c0002t0002g0046 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.113+7660G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702364 | ||||||
| chr6:129702473
|
T | A | 1 | a0002c0002t0001g0047 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.113+7551A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702473 | ||||||
| chr6:129702603
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0002g0170 | 2 | HG01361.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.113+7421A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702603 | ||||||
| chr6:129702740
|
C | T | 26 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0153others(23): Show | 26 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.113+7284G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702740 | ||||||
| chr6:129702771
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0002g0145a0001c0001t0019g0233 | 3 | HG02280.hp2 HG02451.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.113+7253C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702771 | ||||||
| chr6:129702873
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(63): Show | 67 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.113+7151C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702873 | ||||||
| chr6:129702881
|
T | A | 1 | a0001c0001t0004g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.113+7143A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129702881 | ||||||
| chr6:129703003
|
CA | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(179): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.113+7020delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129703003 | ||||||
| chr6:129703055
|
G | A | 73 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(70): Show | 73 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.113+6969C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129703055 | ||||||
| chr6:129703309
|
C | G | 5 | a0001c0001t0001g0099a0001c0001t0001g0129a0001c0001t0001g0130others(2): Show | 5 | HG00735.hp2 HG01106.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.113+6715G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129703309 | ||||||
| chr6:129703442
|
C | A | 1 | a0001c0001t0004g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.113+6582G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129703442 | ||||||
| chr6:129703461
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.113+6563C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129703461 | ||||||
| chr6:129703484
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(98): Show | 102 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.113+6540T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129703484 | ||||||
| chr6:129703882
|
C | T | 1 | a0001c0001t0003g0205 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.113+6142G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129703882 | ||||||
| chr6:129703925
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.113+6099G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129703925 | ||||||
| chr6:129703996
|
GTAA | G | 174 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.113+6025_113+6027d others(5): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129703996 | ||||||
| chr6:129704006
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.113+6018T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704006 | ||||||
| chr6:129704106
|
G | A | 2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+5918C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704106 | ||||||
| chr6:129704113
|
TCTTA | T | 64 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(61): Show | 65 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.113+5907_113+5910d others(6): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704113 | ||||||
| chr6:129704170
|
C | T | 3 | a0001c0001t0001g0098a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG01358.hp1 HG02280.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.113+5854G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704170 | ||||||
| chr6:129704286
|
T | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0067a0001c0001t0001g0072others(63): Show | 67 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.113+5738A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704286 | ||||||
| chr6:129704360
|
G | A | 1 | a0001c0001t0006g0060 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.113+5664C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704360 | ||||||
| chr6:129704369
|
T | C | 1 | a0001c0001t0008g0228 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.113+5655A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704369 | ||||||
| chr6:129704520
|
T | C | 3 | a0001c0001t0001g0124a0001c0001t0001g0126a0001c0001t0002g0125 | 3 | HG02257.hp1 HG03041.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.113+5504A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704520 | ||||||
| chr6:129704535
|
T | A | 1 | a0001c0001t0001g0084 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.113+5489A>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704535 | ||||||
| chr6:129704640
|
T | C | 174 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.113+5384A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704640 | ||||||
| chr6:129704701
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.113+5323G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704701 | ||||||
| chr6:129704800
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.113+5224G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704800 | ||||||
| chr6:129704927
|
T | C | 3 | a0001c0001t0002g0229a0001c0001t0002g0230a0007c0008t0004g0055 | 3 | HG02615.hp2 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.113+5097A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129704927 | ||||||
| chr6:129705097
|
G | T | 1 | a0001c0001t0002g0171 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.113+4927C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129705097 | ||||||
| chr6:129705253
|
A | T | 1 | a0001c0001t0001g0193 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.113+4771T>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129705253 | ||||||
| chr6:129705298
|
C | G | 47 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(44): Show | 47 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.113+4726G>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129705298 | ||||||
| chr6:129705320
|
G | C | 1 | a0007c0008t0004g0055 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.113+4704C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129705320 | ||||||
| chr6:129705664
|
G | T | 27 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0150others(24): Show | 27 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.113+4360C>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129705664 | ||||||
| chr6:129706015
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.113+4009G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706015 | ||||||
| chr6:129706076
|
A | C | 1 | a0002c0002t0001g0054 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.113+3948T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706076 | ||||||
| chr6:129706175
|
G | A | 154 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.113+3849C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706175 | ||||||
| chr6:129706218
|
G | A | 3 | a0001c0001t0001g0191a0001c0001t0003g0058a0001c0001t0003g0059 | 3 | HG00639.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+3806C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706218 | ||||||
| chr6:129706227
|
C | A | 1 | a0002c0002t0001g0048 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.113+3797G>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706227 | ||||||
| chr6:129706619
|
G | C | 36 | a0001c0001t0001g0135a0001c0001t0001g0144a0001c0001t0001g0201others(33): Show | 36 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.113+3405C>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706619 | ||||||
| chr6:129706739
|
T | C | 36 | a0001c0001t0001g0135a0001c0001t0001g0144a0001c0001t0001g0201others(33): Show | 36 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.113+3285A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706739 | ||||||
| chr6:129706841
|
G | A | 35 | a0001c0001t0001g0135a0001c0001t0001g0144a0001c0001t0001g0201others(32): Show | 35 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.113+3183C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706841 | ||||||
| chr6:129706885
|
C | CA | 9 | a0001c0001t0001g0096a0001c0001t0001g0192a0001c0001t0001g0193others(6): Show | 9 | HG01081.hp2 HG01433.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.113+3138dupT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706885 | ||||||
| chr6:129706885
|
CA | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(98): Show | 102 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.113+3138delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706885 | ||||||
| chr6:129706889
|
A | C | 1 | a0002c0002t0001g0008 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.113+3135T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706889 | ||||||
| chr6:129706935
|
A | G | 4 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0003g0128others(1): Show | 4 | HG02280.hp1 HG02970.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.113+3089T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706935 | ||||||
| chr6:129706952
|
C | T | 48 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(45): Show | 48 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.113+3072G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129706952 | ||||||
| chr6:129707017
|
G | A | 2 | a0001c0001t0006g0198a0006c0010t0001g0197 | 2 | HG03704.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.113+3007C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707017 | ||||||
| chr6:129707025
|
G | A | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG00099.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.113+2999C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707025 | ||||||
| chr6:129707115
|
C | T | 40 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(37): Show | 40 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.113+2909G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707115 | ||||||
| chr6:129707125
|
A | G | 1 | a0002c0002t0001g0007 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.113+2899T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707125 | ||||||
| chr6:129707245
|
G | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.113+2779C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707245 | ||||||
| chr6:129707397
|
T | G | 50 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.113+2627A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707397 | ||||||
| chr6:129707406
|
A | C | 150 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.113+2618T>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707406 | ||||||
| chr6:129707530
|
G | A | 64 | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0146others(61): Show | 64 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.113+2494C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707530 | ||||||
| chr6:129707557
|
T | C | 50 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.113+2467A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707557 | ||||||
| chr6:129707619
|
A | G | 50 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0089others(47): Show | 50 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.113+2405T>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707619 | ||||||
| chr6:129707650
|
GT | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(220): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.113+2373delA | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707650 | ||||||
| chr6:129707656
|
T | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG00741.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.113+2368A>C | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129707656 | ||||||
| chr6:129708548
|
G | A | 3 | a0001c0001t0002g0057a0001c0001t0003g0058a0001c0001t0003g0059 | 3 | HG02818.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.113+1476C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129708548 | ||||||
| chr6:129708694
|
G | A | 34 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0203others(31): Show | 34 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.113+1330C>T | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129708694 | ||||||
| chr6:129708742
|
T | C | 1 | a0001c0001t0019g0233 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.113+1282A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129708742 | ||||||
| chr6:129708805
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.113+1219G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129708805 | ||||||
| chr6:129708824
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.113+1200A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129708824 | ||||||
| chr6:129708868
|
T | C | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG01106.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.113+1156A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129708868 | ||||||
| chr6:129708969
|
C | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(25): Show | 29 | HG00140.hp1 HG00438.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.113+1055G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129708969 | ||||||
| chr6:129709287
|
GA | G | 5 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 5 | HG00140.hp1 HG00735.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.113+736delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129709287 | ||||||
| chr6:129709417
|
C | T | 1 | a0001c0001t0006g0060 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.113+607G>A | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129709417 | ||||||
| chr6:129709572
|
GA | G | 4 | a0001c0001t0002g0057a0001c0001t0003g0058a0001c0001t0003g0059others(1): Show | 4 | HG02818.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.113+451delT | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129709572 | ||||||
| chr6:129709712
|
T | C | 1 | a0001c0001t0003g0237 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.113+312A>G | ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | 129709712 |