Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 57514 |
|---|---|
| ensemblid | ENSG00000031081.11 |
| hgncid | 29216 |
| symbol | ARHGAP31 |
| name | Rho GTPase activating protein 31 |
| refseq_nuc | NM_020754.4 |
| refseq_prot | NP_065805.2 |
| ensembl_nuc | ENST00000264245.9 |
| ensembl_prot | ENSP00000264245.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 119294383 |
| end | 119420714 |
| strand | + |
| ver | v1.2 |
| region | chr3:119294383-119420714 |
| region5000 | chr3:119289383-119425714 |
| regionname0 | ARHGAP31_chr3_119294383_119420714 |
| regionname5000 | ARHGAP31_chr3_119289383_119425714 |
| 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 | 1444 | 234 | 59 | 41 | 93 | 6 | 35 | 73 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0002 | 1/1 | 1444 | 44 | 6 | 10 | 16 | 2 | 8 | 9 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0003 | 0/0 | 1444 | 11 | 9 | 2 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0004 | 0/0 | 1444 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0005 | 0/0 | 1444 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0006 | 0/0 | 1444 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0007 | 0/0 | 1444 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0008 | 0/0 | 1444 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0009 | 0/0 | 1444 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0010 | 0/0 | 1444 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0011 | 0/0 | 1444 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0012 | 0/0 | 1444 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0013 | 0/0 | 1444 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0014 | 0/0 | 1444 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0015 | 0/0 | 1444 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| 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 | 4335 | 107 | 11 | 26 | 48 | 4 | 18 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0002 | 0/0 | 4335 | 51 | 10 | 3 | 30 | 0 | 8 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0003 | 1/1 | 4335 | 43 | 5 | 10 | 16 | 2 | 8 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0004 | 0/0 | 4335 | 38 | 7 | 10 | 10 | 2 | 9 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0005 | 0/0 | 4335 | 37 | 30 | 2 | 5 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0006 | 0/0 | 4335 | 9 | 8 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0007 | 0/0 | 4335 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0008 | 0/0 | 4335 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0009 | 0/0 | 4335 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0010 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0011 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0012 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0013 | 0/0 | 4335 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0014 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0015 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0016 | 0/0 | 4335 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0017 | 0/0 | 4335 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0018 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0019 | 0/0 | 4335 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0020 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| c0021 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| 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 | 0/0 | 4974 | 42 | 25 | 3 | 11 | 0 | 3 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0002 | 1/1 | 4973 | 25 | 2 | 4 | 12 | 0 | 5 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0003 | 0/0 | 4974 | 21 | 3 | 5 | 8 | 1 | 4 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0004 | 0/0 | 4974 | 19 | 6 | 1 | 8 | 0 | 4 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0005 | 0/0 | 4974 | 18 | 0 | 3 | 10 | 2 | 3 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0006 | 0/0 | 4973 | 18 | 0 | 5 | 10 | 1 | 2 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0007 | 0/0 | 4974 | 17 | 1 | 4 | 10 | 0 | 2 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0008 | 0/0 | 4973 | 17 | 0 | 3 | 13 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0009 | 0/0 | 4973 | 12 | 2 | 0 | 6 | 2 | 2 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0010 | 0/0 | 4974 | 10 | 0 | 2 | 3 | 1 | 4 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0011 | 0/0 | 4974 | 10 | 0 | 7 | 2 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0012 | 0/0 | 4974 | 7 | 4 | 2 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0013 | 0/0 | 4970 | 5 | 4 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0014 | 0/0 | 4974 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0015 | 0/0 | 4974 | 5 | 5 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0016 | 0/0 | 4974 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0017 | 0/0 | 4973 | 4 | 0 | 1 | 3 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0018 | 0/0 | 4974 | 4 | 0 | 0 | 1 | 0 | 3 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0019 | 0/0 | 4973 | 4 | 1 | 1 | 1 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0020 | 0/0 | 4974 | 4 | 2 | 0 | 0 | 0 | 2 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0021 | 0/0 | 4974 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0022 | 0/0 | 4970 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0023 | 0/0 | 4974 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0024 | 0/0 | 4974 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0025 | 0/0 | 4973 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0026 | 0/0 | 4973 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0027 | 0/0 | 4970 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0028 | 0/0 | 4974 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0029 | 0/0 | 4973 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0030 | 0/0 | 4973 | 2 | 1 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0031 | 0/0 | 4973 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0032 | 0/0 | 4974 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0033 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0034 | 0/0 | 4974 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0035 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0036 | 0/0 | 4970 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0037 | 0/0 | 4974 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0038 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0039 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0040 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0041 | 0/0 | 4973 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0042 | 0/0 | 4973 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0043 | 0/0 | 4973 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0044 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0045 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0046 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0047 | 0/0 | 4970 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0048 | 0/0 | 4970 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0049 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0050 | 0/0 | 4974 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0051 | 0/0 | 4974 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0052 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0053 | 0/0 | 4973 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0054 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0055 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0056 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0057 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0058 | 0/0 | 4974 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0059 | 0/0 | 4974 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0060 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0061 | 0/0 | 4973 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0062 | 0/0 | 4973 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0063 | 0/0 | 4973 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0064 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0065 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| t0066 | 0/0 | 4974 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| 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 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0141 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| 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 | 4335 | 107 | 11 | 26 | 48 | 4 | 18 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0002 | 0/0 | 4335 | 51 | 10 | 3 | 30 | 0 | 8 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0004 | 0/0 | 4335 | 38 | 7 | 10 | 10 | 2 | 9 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0005 | 0/0 | 4335 | 37 | 30 | 2 | 5 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0010 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0002c0003 | 1/1 | 4335 | 43 | 5 | 10 | 16 | 2 | 8 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0002c0018 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0003c0006 | 0/0 | 4335 | 9 | 8 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0003c0009 | 0/0 | 4335 | 2 | 1 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0004c0007 | 0/0 | 4335 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0005c0008 | 0/0 | 4335 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0006c0011 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0007c0012 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0008c0021 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0009c0017 | 0/0 | 4335 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0010c0016 | 0/0 | 4335 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0011c0019 | 0/0 | 4335 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0012c0015 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0013c0020 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0014c0014 | 0/0 | 4335 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0015c0013 | 0/0 | 4335 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0005 | 0/0 | 9308 | 17 | 0 | 3 | 9 | 2 | 3 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0006 | 0/0 | 9307 | 17 | 0 | 5 | 9 | 1 | 2 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0007 | 0/0 | 9308 | 17 | 1 | 4 | 10 | 0 | 2 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0008 | 0/0 | 9307 | 17 | 0 | 3 | 13 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0011 | 0/0 | 9308 | 10 | 0 | 7 | 2 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0017 | 0/0 | 9307 | 4 | 0 | 1 | 3 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0018 | 0/0 | 9308 | 3 | 0 | 0 | 0 | 0 | 3 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0020 | 0/0 | 9308 | 4 | 2 | 0 | 0 | 0 | 2 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0024 | 0/0 | 9308 | 2 | 0 | 0 | 0 | 0 | 2 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0025 | 0/0 | 9307 | 2 | 0 | 1 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0029 | 0/0 | 9307 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0039 | 0/0 | 9307 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0040 | 0/0 | 9307 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0042 | 0/0 | 9307 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0045 | 0/0 | 9307 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0046 | 0/0 | 9308 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0050 | 0/0 | 9308 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0052 | 0/0 | 9307 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0053 | 0/0 | 9307 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0055 | 0/0 | 9308 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0060 | 0/0 | 9307 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0061 | 0/0 | 9307 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0001t0063 | 0/0 | 9307 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0002t0001 | 0/0 | 9308 | 19 | 3 | 2 | 11 | 0 | 3 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0002t0003 | 0/0 | 9308 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0002t0004 | 0/0 | 9308 | 15 | 3 | 0 | 8 | 0 | 4 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0002t0012 | 0/0 | 9308 | 3 | 2 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0002t0016 | 0/0 | 9308 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0002t0018 | 0/0 | 9308 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0002t0028 | 0/0 | 9308 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0002t0033 | 0/0 | 9308 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0002t0034 | 0/0 | 9308 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0002t0037 | 0/0 | 9308 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0002t0065 | 0/0 | 9308 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0004t0003 | 0/0 | 9308 | 19 | 3 | 5 | 6 | 1 | 4 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0004t0010 | 0/0 | 9308 | 10 | 0 | 2 | 3 | 1 | 4 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0004t0021 | 0/0 | 9308 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0004t0032 | 0/0 | 9308 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0004t0038 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0004t0051 | 0/0 | 9308 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0004t0059 | 0/0 | 9308 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0004t0064 | 0/0 | 9308 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0004t0066 | 0/0 | 9308 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0005t0001 | 0/0 | 9308 | 19 | 18 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0005t0004 | 0/0 | 9308 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0005t0012 | 0/0 | 9308 | 3 | 2 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0005t0014 | 0/0 | 9308 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0005t0023 | 0/0 | 9308 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0005t0027 | 0/0 | 9304 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0005t0036 | 0/0 | 9304 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0005t0047 | 0/0 | 9304 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0005t0048 | 0/0 | 9304 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0005t0049 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0005t0057 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0001c0010t0014 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0002c0003t0002 | 1/1 | 9307 | 20 | 2 | 4 | 7 | 0 | 5 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0002c0003t0009 | 0/0 | 9307 | 12 | 2 | 0 | 6 | 2 | 2 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0002c0003t0019 | 0/0 | 9307 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0002c0003t0026 | 0/0 | 9307 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0002c0003t0030 | 0/0 | 9307 | 2 | 1 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0002c0003t0031 | 0/0 | 9307 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0002c0003t0041 | 0/0 | 9307 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0002c0003t0043 | 0/0 | 9307 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0002c0003t0062 | 0/0 | 9307 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0002c0018t0019 | 0/0 | 9307 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0003c0006t0001 | 0/0 | 9308 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0003c0006t0013 | 0/0 | 9304 | 4 | 3 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0003c0006t0022 | 0/0 | 9304 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0003c0006t0056 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0003c0009t0004 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0003c0009t0012 | 0/0 | 9308 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0004c0007t0015 | 0/0 | 9308 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0004c0007t0044 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0004c0007t0054 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0005c0008t0002 | 0/0 | 9307 | 5 | 0 | 0 | 5 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0006c0011t0015 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0007c0012t0001 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0008c0021t0001 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0009c0017t0019 | 0/0 | 9307 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0010c0016t0004 | 0/0 | 9308 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0011c0019t0005 | 0/0 | 9308 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0012c0015t0035 | 0/0 | 9307 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0013c0020t0013 | 0/0 | 9304 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0014c0014t0058 | 0/0 | 9308 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| a0015c0013t0006 | 0/0 | 9307 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | copy fasta | chr3 | 119289383 | 119425714 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0005g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0005g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0006g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0006g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0006g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0006g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0006g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0007g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0007g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0007g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0007g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0007g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0007g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0007g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0007g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0007g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0007g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0007g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0007g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0007g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0007g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0007g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0007g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0007g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0008g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0008g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0008g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0008g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0008g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0008g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0008g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0008g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0008g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0008g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0008g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0008g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0008g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0008g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0008g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0008g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0008g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0011g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0011g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0011g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0011g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0011g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0011g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0011g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0011g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0011g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0017g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0017g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0017g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0017g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0018g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0018g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0018g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0020g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0020g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0020g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0020g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0024g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0024g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0025g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0025g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0029g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0029g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0039g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0040g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0042g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0045g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0046g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0050g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0052g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0053g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0055g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0060g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0061g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0001t0063g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0004g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0004g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0004g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0012g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0012g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0016g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0016g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0016g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0016g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0016g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0018g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0028g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0028g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0033g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0034g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0037g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0002t0065g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0010g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0010g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0010g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0010g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0010g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0010g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0010g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0010g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0010g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0021g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0021g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0021g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0032g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0038g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0051g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0059g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0064g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0004t0066g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0012g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0012g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0012g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0014g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0014g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0014g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0014g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0023g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0023g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0027g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0027g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0036g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0047g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0048g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0049g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0005t0057g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0001c0010t0014g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0141 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0009g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0009g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0009g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0009g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0009g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0009g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0009g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0009g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0009g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0009g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0009g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0019g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0019g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0026g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0026g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0030g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0030g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0031g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0031g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0041g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0043g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0003t0062g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0002c0018t0019g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0003c0006t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0003c0006t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0003c0006t0013g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0003c0006t0013g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0003c0006t0013g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0003c0006t0013g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0003c0006t0022g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0003c0006t0022g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0003c0006t0056g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0003c0009t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0003c0009t0012g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0004c0007t0015g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0004c0007t0015g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0004c0007t0015g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0004c0007t0015g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0004c0007t0044g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0004c0007t0054g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0005c0008t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0005c0008t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0005c0008t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0005c0008t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0005c0008t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0006c0011t0015g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0007c0012t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0008c0021t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0009c0017t0019g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0010c0016t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0011c0019t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0012c0015t0035g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0013c0020t0013g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0014c0014t0058g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| a0015c0013t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0077 | EUR | GBR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00099 | hp2 | a0001 | c0004 | t0010 | g0222 | EUR | GBR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00280 | hp1 | a0001 | c0001 | t0042 | g0282 | EUR | FIN | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00280 | hp2 | a0002 | c0003 | t0009 | g0167 | EUR | FIN | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0148 | EUR | FIN | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0078 | EUR | FIN | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | CHS | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00408 | hp2 | a0001 | c0001 | t0008 | g0213 | EAS | CHS | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00438 | hp1 | a0001 | c0005 | t0047 | g0239 | EAS | CHS | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00438 | hp2 | a0001 | c0002 | t0016 | g0133 | EAS | CHS | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00597 | hp1 | a0001 | c0002 | t0012 | g0238 | EAS | CHS | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00597 | hp2 | a0002 | c0003 | t0062 | g0093 | EAS | CHS | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0168 | EAS | CHS | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00609 | hp2 | a0001 | c0001 | t0007 | g0254 | EAS | CHS | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00621 | hp1 | a0002 | c0003 | t0009 | g0248 | EAS | CHS | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00621 | hp2 | a0002 | c0003 | t0009 | g0245 | EAS | CHS | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00639 | hp1 | a0001 | c0005 | t0012 | g0288 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0293 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00735 | hp1 | a0001 | c0001 | t0011 | g0186 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00735 | hp2 | a0010 | c0016 | t0004 | g0166 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0296 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00741 | hp1 | a0002 | c0003 | t0041 | g0295 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG00741 | hp2 | a0001 | c0004 | t0003 | g0113 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01071 | hp1 | a0001 | c0001 | t0017 | g0189 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0075 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01081 | hp1 | a0001 | c0001 | t0053 | g0187 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01081 | hp2 | a0001 | c0001 | t0011 | g0292 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01099 | hp1 | a0003 | c0006 | t0013 | g0031 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01099 | hp2 | a0001 | c0004 | t0059 | g0015 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01106 | hp1 | a0002 | c0003 | t0002 | g0145 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01106 | hp2 | a0003 | c0009 | t0012 | g0290 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01167 | hp1 | a0001 | c0004 | t0010 | g0267 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01167 | hp2 | a0001 | c0001 | t0006 | g0100 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01168 | hp1 | a0002 | c0003 | t0002 | g0123 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01168 | hp2 | a0001 | c0004 | t0032 | g0071 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0127 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01192 | hp2 | a0001 | c0002 | t0034 | g0240 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0102 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01243 | hp2 | a0001 | c0005 | t0001 | g0012 | AMR | PUR | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01255 | hp1 | a0001 | c0001 | t0008 | g0216 | AMR | CLM | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01255 | hp2 | a0001 | c0004 | t0003 | g0024 | AMR | CLM | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01256 | hp1 | a0001 | c0004 | t0003 | g0125 | AMR | CLM | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01256 | hp2 | a0001 | c0001 | t0007 | g0226 | AMR | CLM | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01258 | hp1 | a0001 | c0001 | t0007 | g0227 | AMR | CLM | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01258 | hp2 | a0002 | c0003 | t0002 | g0118 | AMR | CLM | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01261 | hp1 | a0001 | c0001 | t0008 | g0215 | AMR | CLM | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01261 | hp2 | a0001 | c0004 | t0066 | g0217 | AMR | CLM | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01358 | hp1 | a0001 | c0001 | t0011 | g0001 | AMR | CLM | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01358 | hp2 | a0002 | c0003 | t0002 | g0112 | AMR | CLM | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01361 | hp1 | a0002 | c0003 | t0019 | g0182 | AMR | CLM | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01361 | hp2 | a0001 | c0001 | t0063 | g0139 | AMR | CLM | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01496 | hp1 | a0001 | c0004 | t0003 | g0007 | AMR | CLM | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01496 | hp2 | a0002 | c0003 | t0031 | g0089 | AMR | CLM | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01884 | hp1 | a0004 | c0007 | t0015 | g0016 | AFR | ACB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01884 | hp2 | a0003 | c0006 | t0056 | g0011 | AFR | ACB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01934 | hp1 | a0001 | c0001 | t0011 | g0188 | AMR | PEL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01934 | hp2 | a0001 | c0001 | t0025 | g0223 | AMR | PEL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01943 | hp1 | a0001 | c0001 | t0011 | g0184 | AMR | PEL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01943 | hp2 | a0001 | c0001 | t0006 | g0073 | AMR | PEL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01975 | hp1 | a0002 | c0003 | t0026 | g0232 | AMR | PEL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01975 | hp2 | a0001 | c0001 | t0005 | g0022 | AMR | PEL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01978 | hp1 | a0001 | c0001 | t0011 | g0001 | AMR | PEL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01978 | hp2 | a0002 | c0003 | t0031 | g0138 | AMR | PEL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01993 | hp1 | a0001 | c0001 | t0011 | g0158 | AMR | PEL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0027 | AMR | PEL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02015 | hp1 | a0002 | c0003 | t0002 | g0082 | EAS | KHV | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02015 | hp2 | a0001 | c0005 | t0027 | g0044 | EAS | KHV | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02055 | hp1 | a0001 | c0004 | t0021 | g0059 | AFR | ACB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02055 | hp2 | a0003 | c0006 | t0022 | g0270 | AFR | ACB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02056 | hp1 | a0001 | c0002 | t0004 | g0211 | EAS | KHV | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02056 | hp2 | a0002 | c0003 | t0002 | g0090 | EAS | KHV | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0278 | EAS | KHV | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02080 | hp2 | a0001 | c0001 | t0008 | g0212 | EAS | KHV | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02083 | hp1 | a0001 | c0005 | t0048 | g0304 | EAS | KHV | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | KHV | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02129 | hp1 | a0001 | c0001 | t0011 | g0301 | EAS | KHV | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02129 | hp2 | a0001 | c0004 | t0003 | g0120 | EAS | KHV | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02135 | hp1 | a0001 | c0001 | t0008 | g0199 | EAS | KHV | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02135 | hp2 | a0002 | c0003 | t0009 | g0268 | EAS | KHV | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02145 | hp1 | a0001 | c0005 | t0001 | g0069 | AFR | ACB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02145 | hp2 | a0001 | c0001 | t0007 | g0275 | AFR | ACB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02148 | hp1 | a0001 | c0001 | t0008 | g0192 | AMR | PEL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02148 | hp2 | a0001 | c0004 | t0010 | g0195 | AMR | PEL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02155 | hp1 | a0001 | c0002 | t0016 | g0279 | EAS | CDX | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02155 | hp2 | a0005 | c0008 | t0002 | g0122 | EAS | CDX | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02257 | hp1 | a0001 | c0005 | t0001 | g0046 | AFR | ACB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02257 | hp2 | a0001 | c0002 | t0012 | g0206 | AFR | ACB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02258 | hp1 | a0001 | c0005 | t0001 | g0049 | AFR | ACB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02258 | hp2 | a0004 | c0007 | t0015 | g0052 | AFR | ACB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02280 | hp1 | a0001 | c0005 | t0001 | g0034 | AFR | ACB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02280 | hp2 | a0001 | c0010 | t0014 | g0004 | AFR | ACB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02293 | hp1 | a0002 | c0003 | t0026 | g0294 | AMR | PEL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0111 | AMR | PEL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02300 | hp1 | a0001 | c0001 | t0005 | g0096 | AMR | PEL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02300 | hp2 | a0001 | c0004 | t0003 | g0072 | AMR | PEL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02451 | hp1 | a0003 | c0006 | t0001 | g0159 | AFR | ACB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02451 | hp2 | a0001 | c0004 | t0003 | g0040 | AFR | ACB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02523 | hp1 | a0002 | c0003 | t0019 | g0308 | EAS | KHV | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02523 | hp2 | a0001 | c0002 | t0018 | g0305 | EAS | KHV | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02572 | hp1 | a0001 | c0005 | t0001 | g0163 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02572 | hp2 | a0004 | c0007 | t0015 | g0030 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02602 | hp1 | a0001 | c0001 | t0007 | g0241 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0080 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02615 | hp1 | a0001 | c0001 | t0052 | g0283 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02615 | hp2 | a0001 | c0002 | t0004 | g0247 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02622 | hp1 | a0001 | c0004 | t0003 | g0038 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02622 | hp2 | a0001 | c0005 | t0001 | g0160 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02630 | hp1 | a0001 | c0001 | t0045 | g0286 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02630 | hp2 | a0001 | c0005 | t0001 | g0067 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02647 | hp1 | a0001 | c0005 | t0023 | g0198 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02647 | hp2 | a0001 | c0005 | t0001 | g0020 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02683 | hp1 | a0001 | c0001 | t0020 | g0043 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02683 | hp2 | a0001 | c0001 | t0050 | g0177 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02698 | hp1 | a0002 | c0003 | t0030 | g0149 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02698 | hp2 | a0001 | c0001 | t0007 | g0276 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02717 | hp1 | a0003 | c0006 | t0013 | g0045 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02717 | hp2 | a0001 | c0005 | t0001 | g0164 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02723 | hp1 | a0012 | c0015 | t0035 | g0237 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0014 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02735 | hp1 | a0001 | c0004 | t0003 | g0076 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02735 | hp2 | a0001 | c0001 | t0005 | g0142 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02738 | hp1 | a0001 | c0004 | t0010 | g0219 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02738 | hp2 | a0001 | c0001 | t0008 | g0224 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02818 | hp1 | a0001 | c0005 | t0004 | g0258 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02818 | hp2 | a0003 | c0006 | t0013 | g0006 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02886 | hp1 | a0001 | c0005 | t0057 | g0033 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02886 | hp2 | a0001 | c0004 | t0003 | g0039 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02895 | hp1 | a0004 | c0007 | t0044 | g0196 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02895 | hp2 | a0001 | c0005 | t0001 | g0035 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02896 | hp1 | a0001 | c0002 | t0028 | g0018 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02896 | hp2 | a0001 | c0001 | t0040 | g0257 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02897 | hp1 | a0001 | c0005 | t0001 | g0037 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02897 | hp2 | a0001 | c0002 | t0028 | g0017 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02922 | hp1 | a0003 | c0006 | t0013 | g0041 | AFR | ESN | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02922 | hp2 | a0001 | c0004 | t0021 | g0048 | AFR | ESN | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0070 | AFR | ESN | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02970 | hp2 | a0001 | c0001 | t0020 | g0010 | AFR | ESN | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02976 | hp1 | a0001 | c0004 | t0038 | g0181 | AFR | ESN | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ESN | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03017 | hp1 | a0001 | c0004 | t0010 | g0197 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03017 | hp2 | a0002 | c0003 | t0002 | g0060 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03041 | hp1 | a0001 | c0005 | t0001 | g0191 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03041 | hp2 | a0002 | c0003 | t0030 | g0053 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03098 | hp1 | a0002 | c0003 | t0009 | g0220 | AFR | MSL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03098 | hp2 | a0001 | c0005 | t0014 | g0028 | AFR | MSL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03130 | hp1 | a0001 | c0005 | t0014 | g0047 | AFR | ESN | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03130 | hp2 | a0001 | c0001 | t0020 | g0056 | AFR | ESN | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03139 | hp1 | a0003 | c0006 | t0001 | g0161 | AFR | ESN | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03139 | hp2 | a0001 | c0005 | t0014 | g0009 | AFR | ESN | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03195 | hp1 | a0001 | c0001 | t0060 | g0026 | AFR | ESN | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03195 | hp2 | a0002 | c0003 | t0009 | g0265 | AFR | ESN | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03209 | hp1 | a0001 | c0001 | t0039 | g0260 | AFR | MSL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03209 | hp2 | a0001 | c0005 | t0001 | g0036 | AFR | MSL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03225 | hp1 | a0001 | c0005 | t0001 | g0019 | AFR | MSL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0203 | AFR | MSL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03239 | hp1 | a0001 | c0004 | t0003 | g0147 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03239 | hp2 | a0001 | c0001 | t0020 | g0064 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03486 | hp1 | a0001 | c0005 | t0023 | g0193 | AFR | MSL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03486 | hp2 | a0001 | c0005 | t0014 | g0062 | AFR | MSL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03490 | hp1 | a0002 | c0003 | t0009 | g0298 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03490 | hp2 | a0001 | c0002 | t0004 | g0236 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03491 | hp1 | a0001 | c0001 | t0025 | g0204 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0065 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0066 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03492 | hp2 | a0002 | c0003 | t0009 | g0297 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03516 | hp1 | a0002 | c0003 | t0002 | g0032 | AFR | ESN | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03516 | hp2 | a0001 | c0005 | t0012 | g0287 | AFR | ESN | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03540 | hp1 | a0001 | c0005 | t0004 | g0253 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03540 | hp2 | a0002 | c0018 | t0019 | g0284 | AFR | GWD | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03579 | hp1 | a0007 | c0012 | t0001 | g0050 | AFR | MSL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03579 | hp2 | a0001 | c0001 | t0029 | g0042 | AFR | MSL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03654 | hp1 | a0001 | c0001 | t0018 | g0209 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03654 | hp2 | a0009 | c0017 | t0019 | g0185 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03669 | hp1 | a0002 | c0003 | t0002 | g0152 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03669 | hp2 | a0001 | c0004 | t0010 | g0176 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03704 | hp1 | a0001 | c0002 | t0037 | g0214 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03704 | hp2 | a0001 | c0004 | t0051 | g0157 | SAS | PJL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0087 | SAS | BEB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03831 | hp2 | a0001 | c0004 | t0010 | g0274 | SAS | BEB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03834 | hp1 | a0001 | c0004 | t0003 | g0128 | SAS | BEB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03834 | hp2 | a0001 | c0001 | t0018 | g0207 | SAS | BEB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03927 | hp1 | a0001 | c0004 | t0003 | g0136 | SAS | BEB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03927 | hp2 | a0001 | c0002 | t0004 | g0291 | SAS | BEB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG04115 | hp1 | a0001 | c0002 | t0004 | g0235 | SAS | STU | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG04115 | hp2 | a0002 | c0003 | t0002 | g0137 | SAS | STU | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG04184 | hp1 | a0001 | c0001 | t0024 | g0221 | SAS | BEB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0153 | SAS | BEB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0074 | SAS | STU | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG04199 | hp2 | a0001 | c0001 | t0011 | g0183 | SAS | STU | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0088 | SAS | STU | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG04204 | hp2 | a0001 | c0002 | t0004 | g0233 | SAS | STU | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG04228 | hp1 | a0001 | c0001 | t0018 | g0208 | SAS | STU | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG04228 | hp2 | a0002 | c0003 | t0002 | g0151 | SAS | STU | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18522 | hp1 | a0001 | c0005 | t0001 | g0190 | AFR | YRI | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18522 | hp2 | a0001 | c0005 | t0001 | g0029 | AFR | YRI | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18612 | hp1 | a0001 | c0001 | t0005 | g0172 | EAS | CHB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18612 | hp2 | a0001 | c0002 | t0033 | g0231 | EAS | CHB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18906 | hp1 | a0001 | c0002 | t0012 | g0174 | AFR | YRI | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18906 | hp2 | a0001 | c0005 | t0001 | g0165 | AFR | YRI | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18940 | hp1 | a0001 | c0001 | t0007 | g0249 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18940 | hp2 | a0001 | c0001 | t0011 | g0300 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18944 | hp2 | a0001 | c0004 | t0010 | g0002 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18945 | hp1 | a0002 | c0003 | t0002 | g0085 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18945 | hp2 | a0005 | c0008 | t0002 | g0107 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18946 | hp1 | a0001 | c0001 | t0008 | g0229 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18946 | hp2 | a0001 | c0001 | t0005 | g0129 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18950 | hp2 | a0001 | c0001 | t0008 | g0277 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18952 | hp1 | a0002 | c0003 | t0009 | g0201 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18952 | hp2 | a0001 | c0005 | t0027 | g0130 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18953 | hp1 | a0001 | c0001 | t0006 | g0131 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18953 | hp2 | a0001 | c0002 | t0016 | g0099 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18956 | hp1 | a0001 | c0004 | t0010 | g0244 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18956 | hp2 | a0001 | c0001 | t0006 | g0124 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18957 | hp1 | a0002 | c0003 | t0002 | g0081 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18957 | hp2 | a0001 | c0001 | t0008 | g0299 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18960 | hp1 | a0001 | c0001 | t0007 | g0251 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18960 | hp2 | a0001 | c0004 | t0003 | g0110 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18962 | hp1 | a0002 | c0003 | t0002 | g0079 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18962 | hp2 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18964 | hp1 | a0002 | c0003 | t0043 | g0210 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18964 | hp2 | a0001 | c0002 | t0004 | g0242 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18969 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18971 | hp1 | a0001 | c0001 | t0017 | g0175 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18971 | hp2 | a0001 | c0004 | t0003 | g0126 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18975 | hp1 | a0001 | c0001 | t0006 | g0092 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18981 | hp1 | a0001 | c0001 | t0007 | g0250 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18981 | hp2 | a0001 | c0001 | t0006 | g0154 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18985 | hp1 | a0001 | c0001 | t0005 | g0156 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18985 | hp2 | a0001 | c0001 | t0008 | g0180 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18987 | hp1 | a0002 | c0003 | t0009 | g0264 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18990 | hp1 | a0001 | c0001 | t0007 | g0272 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18990 | hp2 | a0001 | c0005 | t0036 | g0271 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18992 | hp1 | a0015 | c0013 | t0006 | g0115 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18992 | hp2 | a0001 | c0001 | t0007 | g0228 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18994 | hp1 | a0001 | c0001 | t0006 | g0094 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18994 | hp2 | a0001 | c0004 | t0003 | g0021 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0143 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18995 | hp2 | a0001 | c0004 | t0010 | g0002 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18998 | hp1 | a0001 | c0002 | t0016 | g0098 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18998 | hp2 | a0001 | c0002 | t0004 | g0262 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18999 | hp1 | a0001 | c0001 | t0008 | g0170 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18999 | hp2 | a0001 | c0002 | t0004 | g0246 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0225 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19000 | hp2 | a0001 | c0001 | t0006 | g0109 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19003 | hp1 | a0001 | c0001 | t0006 | g0104 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19003 | hp2 | a0001 | c0002 | t0004 | g0266 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19005 | hp1 | a0011 | c0019 | t0005 | g0155 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19005 | hp2 | a0001 | c0001 | t0008 | g0178 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19011 | hp1 | a0001 | c0001 | t0007 | g0259 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19011 | hp2 | a0001 | c0004 | t0003 | g0280 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19043 | hp1 | a0008 | c0021 | t0001 | g0068 | AFR | LWK | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19043 | hp2 | a0003 | c0006 | t0022 | g0269 | AFR | LWK | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19058 | hp1 | a0001 | c0001 | t0006 | g0103 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19060 | hp1 | a0001 | c0001 | t0046 | g0307 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19062 | hp2 | a0001 | c0002 | t0004 | g0255 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19064 | hp1 | a0001 | c0001 | t0008 | g0273 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19064 | hp2 | a0005 | c0008 | t0002 | g0116 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19066 | hp1 | a0001 | c0004 | t0003 | g0095 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19066 | hp2 | a0001 | c0002 | t0016 | g0097 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19067 | hp1 | a0001 | c0002 | t0004 | g0179 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19067 | hp2 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19070 | hp1 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19075 | hp1 | a0002 | c0003 | t0002 | g0218 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19075 | hp2 | a0001 | c0001 | t0008 | g0281 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19081 | hp1 | a0001 | c0001 | t0017 | g0302 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19081 | hp2 | a0001 | c0001 | t0055 | g0306 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19083 | hp1 | a0001 | c0004 | t0064 | g0061 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19083 | hp2 | a0002 | c0003 | t0009 | g0263 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19084 | hp1 | a0005 | c0008 | t0002 | g0114 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19084 | hp2 | a0001 | c0001 | t0008 | g0252 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19086 | hp1 | a0002 | c0003 | t0002 | g0119 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19086 | hp2 | a0001 | c0001 | t0017 | g0303 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19087 | hp1 | a0005 | c0008 | t0002 | g0106 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19087 | hp2 | a0001 | c0002 | t0004 | g0230 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19090 | hp1 | a0001 | c0001 | t0007 | g0202 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19091 | hp1 | a0001 | c0001 | t0008 | g0200 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19091 | hp2 | a0001 | c0002 | t0065 | g0091 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19240 | hp1 | a0001 | c0005 | t0049 | g0289 | AFR | YRI | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA19240 | hp2 | a0004 | c0007 | t0054 | g0205 | AFR | YRI | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA20129 | hp1 | a0001 | c0002 | t0004 | g0256 | AFR | ASW | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA20129 | hp2 | a0001 | c0001 | t0029 | g0054 | AFR | ASW | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA20805 | hp1 | a0001 | c0004 | t0003 | g0150 | EUR | TSI | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA20805 | hp2 | a0002 | c0003 | t0009 | g0194 | EUR | TSI | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA20905 | hp1 | a0001 | c0001 | t0024 | g0243 | SAS | GIH | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA20905 | hp2 | a0002 | c0003 | t0002 | g0063 | SAS | GIH | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02486 | hp1 | a0001 | c0001 | t0061 | g0057 | AFR | ACB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02486 | hp2 | a0014 | c0014 | t0058 | g0003 | AFR | ACB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02559 | hp1 | a0001 | c0005 | t0012 | g0285 | AFR | ACB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG02559 | hp2 | a0001 | c0005 | t0001 | g0005 | AFR | ACB | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03471 | hp1 | a0006 | c0011 | t0015 | g0013 | AFR | MSL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG03471 | hp2 | a0001 | c0004 | t0021 | g0055 | AFR | MSL | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG06807 | hp1 | a0003 | c0009 | t0004 | g0261 | AFR | USA | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| HG06807 | hp2 | a0002 | c0003 | t0002 | g0086 | AFR | USA | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18955 | hp1 | a0001 | c0001 | t0007 | g0234 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA18955 | hp2 | a0001 | c0002 | t0003 | g0144 | EAS | JPT | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA21309 | hp1 | a0004 | c0007 | t0015 | g0162 | AFR | LWK | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| NA21309 | hp2 | a0013 | c0020 | t0013 | g0051 | AFR | LWK | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0002 | g0146 | REF | REF | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| homoSapiens_grch38 | hp1 | a0002 | c0003 | t0002 | g0141 | REF | REF | ARHGAP31_chr3_119289383_119425714 | ARHGAP31 | chr3 | 119289383 | 119425714 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:119382312
|
G | A | 2 | a0006a0007 | 2 | HG03471.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.452G>A | p.Arg151Gln | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 5/12 | 974/9307 | 452/4335 | 151/1444 | chr3 | 119382312 | ||
| chr3:119402133
|
C | A | 1 | a0015 | 1 | NA18992.hp1 | missense_variant | MODERATE | c.1381C>A | p.Pro461Thr | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/12 | 1903/9307 | 1381/4335 | 461/1444 | chr3 | 119402133 | ||
| chr3:119402349
|
G | A | 1 | a0014 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.1597G>A | p.Gly533Arg | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/12 | 2119/9307 | 1597/4335 | 533/1444 | chr3 | 119402349 | ||
| chr3:119402370
|
A | G | 1 | a0008 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1618A>G | p.Lys540Glu | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/12 | 2140/9307 | 1618/4335 | 540/1444 | chr3 | 119402370 | ||
| chr3:119409550
|
C | T | 2 | a0004a0006 | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
missense_variant | MODERATE | c.1700C>T | p.Pro567Leu | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/12 | 2222/9307 | 1700/4335 | 567/1444 | chr3 | 119409550 | ||
| chr3:119409622
|
A | G | 1 | a0013 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1772A>G | p.Glu591Gly | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/12 | 2294/9307 | 1772/4335 | 591/1444 | chr3 | 119409622 | ||
| chr3:119414273
|
C | A | 1 | a0012 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.2344C>A | p.Pro782Thr | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 2866/9307 | 2344/4335 | 782/1444 | chr3 | 119414273 | ||
| chr3:119414288
|
C | T | 1 | a0011 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.2359C>T | p.Pro787Ser | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 2881/9307 | 2359/4335 | 787/1444 | chr3 | 119414288 | ||
| chr3:119414336
|
G | A | 12 | a0001a0003a0004others(9): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
missense_variant | MODERATE | c.2407G>A | p.Gly803Ser | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 2929/9307 | 2407/4335 | 803/1444 | chr3 | 119414336 | ||
| chr3:119414441
|
G | C | 1 | a0009 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.2512G>C | p.Glu838Gln | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3034/9307 | 2512/4335 | 838/1444 | chr3 | 119414441 | ||
| chr3:119415185
|
G | A | 2 | a0003a0013 | 12 | HG01099.hp1 HG01106.hp2 HG01884.hp2 others(9): Show |
missense_variant | MODERATE | c.3256G>A | p.Ala1086Thr | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3778/9307 | 3256/4335 | 1086/1444 | chr3 | 119415185 | ||
| chr3:119415387
|
A | G | 1 | a0010 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.3458A>G | p.Asp1153Gly | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3980/9307 | 3458/4335 | 1153/1444 | chr3 | 119415387 | ||
| chr3:119416025
|
G | A | 1 | a0005 | 5 | HG02155.hp2 NA18945.hp2 NA19064.hp2 others(2): Show |
missense_variant | MODERATE | c.4096G>A | p.Val1366Met | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 4618/9307 | 4096/4335 | 1366/1444 | chr3 | 119416025 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:119380939
|
G | C | 2 | a0001c0010a0003c0009 | 3 | HG01106.hp2 HG02280.hp2 HG06807.hp1 |
synonymous_variant | LOW | c.384G>C | p.Leu128Leu | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/12 | 906/9307 | 384/4335 | 128/1444 | chr3 | 119380939 | ||
| chr3:119383198
|
C | T | 1 | a0003c0009 | 2 | HG01106.hp2 HG06807.hp1 |
synonymous_variant | LOW | c.654C>T | p.Asn218Asn | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/12 | 1176/9307 | 654/4335 | 218/1444 | chr3 | 119383198 | ||
| chr3:119402243
|
C | A | 2 | a0004c0007a0006c0011 | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
synonymous_variant | LOW | c.1491C>A | p.Arg497Arg | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/12 | 2013/9307 | 1491/4335 | 497/1444 | chr3 | 119402243 | ||
| chr3:119402285
|
A | G | 2 | a0004c0007a0006c0011 | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
synonymous_variant | LOW | c.1533A>G | p.Thr511Thr | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/12 | 2055/9307 | 1533/4335 | 511/1444 | chr3 | 119402285 | ||
| chr3:119402366
|
A | G | 2 | a0004c0007a0006c0011 | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
synonymous_variant | LOW | c.1614A>G | p.Glu538Glu | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/12 | 2136/9307 | 1614/4335 | 538/1444 | chr3 | 119402366 | ||
| chr3:119409551
|
G | A | 1 | a0001c0002 | 51 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(48): Show |
synonymous_variant | LOW | c.1701G>A | p.Pro567Pro | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/12 | 2223/9307 | 1701/4335 | 567/1444 | chr3 | 119409551 | ||
| chr3:119414128
|
A | T | 1 | a0001c0010 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.2199A>T | p.Ala733Ala | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 2721/9307 | 2199/4335 | 733/1444 | chr3 | 119414128 | ||
| chr3:119414707
|
G | A | 2 | a0001c0004a0014c0014 | 39 | HG00099.hp2 HG00741.hp2 HG01099.hp2 others(36): Show |
synonymous_variant | LOW | c.2778G>A | p.Ala926Ala | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3300/9307 | 2778/4335 | 926/1444 | chr3 | 119414707 | ||
| chr3:119415001
|
A | G | 1 | a0002c0018 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.3072A>G | p.Gly1024Gly | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3594/9307 | 3072/4335 | 1024/1444 | chr3 | 119415001 | ||
| chr3:119415544
|
C | T | 5 | a0001c0005a0001c0010a0007c0012others(2): Show | 41 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(38): Show |
synonymous_variant | LOW | c.3615C>T | p.Pro1205Pro | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 4137/9307 | 3615/4335 | 1205/1444 | chr3 | 119415544 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:119294545
|
G | A | 1 | a0001c0004t0032 | 1 | HG01168.hp2 | 5_prime_UTR_variant | MODIFIER | c.-360G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/12 | 360 | chr3 | 119294545 | |||||
| chr3:119294610
|
A | G | 1 | a0001c0004t0066 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-295A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/12 | 295 | chr3 | 119294610 | |||||
| chr3:119294650
|
C | A | 1 | a0001c0002t0033 | 1 | NA18612.hp2 | 5_prime_UTR_variant | MODIFIER | c.-255C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/12 | 255 | chr3 | 119294650 | |||||
| chr3:119294711
|
G | A | 26 | a0001c0001t0007a0001c0001t0008a0001c0001t0024others(23): Show | 98 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(95): Show |
5_prime_UTR_variant | MODIFIER | c.-194G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/12 | 194 | chr3 | 119294711 | |||||
| chr3:119294756
|
G | A | 1 | a0001c0002t0034 | 1 | HG01192.hp2 | 5_prime_UTR_variant | MODIFIER | c.-149G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/12 | 149 | chr3 | 119294756 | |||||
| chr3:119294867
|
C | A | 20 | a0001c0001t0011a0001c0001t0017a0001c0001t0018others(17): Show | 39 | HG00438.hp1 HG00597.hp1 HG00639.hp1 others(36): Show |
5_prime_UTR_variant | MODIFIER | c.-38C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/12 | 38 | chr3 | 119294867 | |||||
| chr3:119416298
|
G | A | 1 | a0001c0001t0045 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*34G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 34 | chr3 | 119416298 | |||||
| chr3:119416369
|
T | C | 2 | a0001c0001t0046a0001c0001t0055 | 2 | NA19060.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*105T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 105 | chr3 | 119416369 | |||||
| chr3:119416478
|
T | C | 1 | a0012c0015t0035 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*214T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 214 | chr3 | 119416478 | |||||
| chr3:119416531
|
C | T | 2 | a0001c0002t0016a0001c0002t0033 | 6 | HG00438.hp2 HG02155.hp1 NA18612.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*267C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 267 | chr3 | 119416531 | |||||
| chr3:119416533
|
A | G | 4 | a0004c0007t0015a0004c0007t0044a0004c0007t0054others(1): Show | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*269A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 269 | chr3 | 119416533 | |||||
| chr3:119416708
|
T | C | 1 | a0001c0005t0047 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*444T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 444 | chr3 | 119416708 | |||||
| chr3:119416730
|
C | T | 1 | a0002c0003t0043 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*466C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 466 | chr3 | 119416730 | |||||
| chr3:119416793
|
A | G | 1 | a0001c0002t0065 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*529A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 529 | chr3 | 119416793 | |||||
| chr3:119416854
|
C | G | 2 | a0002c0003t0026a0002c0003t0031 | 4 | HG01496.hp2 HG01975.hp1 HG01978.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*590C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 590 | chr3 | 119416854 | |||||
| chr3:119416854
|
C | T | 1 | a0001c0004t0064 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*590C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 590 | chr3 | 119416854 | |||||
| chr3:119417249
|
A | AC | 61 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(58): Show | 246 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*985_*986insC | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 986 | chr3 | 119417249 | |||||
| chr3:119417331
|
C | T | 1 | a0001c0002t0028 | 2 | HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1067C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 1067 | chr3 | 119417331 | |||||
| chr3:119417354
|
G | A | 1 | a0001c0001t0060 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1090G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 1090 | chr3 | 119417354 | |||||
| chr3:119417390
|
A | T | 4 | a0001c0001t0018a0001c0001t0020a0001c0001t0024others(1): Show | 10 | HG02523.hp2 HG02683.hp1 HG02970.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1126A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 1126 | chr3 | 119417390 | |||||
| chr3:119417420
|
C | G | 4 | a0001c0001t0025a0001c0001t0042a0001c0001t0053others(1): Show | 5 | HG00280.hp1 HG01081.hp1 HG01361.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1156C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 1156 | chr3 | 119417420 | |||||
| chr3:119417440
|
T | G | 4 | a0001c0001t0025a0001c0001t0042a0001c0001t0053others(1): Show | 5 | HG00280.hp1 HG01081.hp1 HG01361.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1176T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 1176 | chr3 | 119417440 | |||||
| chr3:119417483
|
C | T | 2 | a0002c0003t0030a0002c0003t0041 | 3 | HG00741.hp1 HG02698.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1219C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 1219 | chr3 | 119417483 | |||||
| chr3:119417581
|
T | C | 1 | a0001c0001t0060 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1317T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 1317 | chr3 | 119417581 | |||||
| chr3:119417648
|
GCACT | G | 4 | a0001c0005t0027a0001c0005t0036a0001c0005t0047others(1): Show | 5 | HG00438.hp1 HG02015.hp2 HG02083.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1391_*1394delCTCA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 1391 | INFO_REALIGN_3_PRIME | chr3 | 119417648 | ||||
| chr3:119417650
|
A | T | 1 | a0001c0001t0042 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1386A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 1386 | chr3 | 119417650 | |||||
| chr3:119417921
|
C | T | 4 | a0001c0001t0018a0001c0001t0020a0001c0001t0024others(1): Show | 10 | HG02523.hp2 HG02683.hp1 HG02970.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1657C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 1657 | chr3 | 119417921 | |||||
| chr3:119417956
|
G | T | 2 | a0002c0003t0030a0002c0003t0041 | 3 | HG00741.hp1 HG02698.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1692G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 1692 | chr3 | 119417956 | |||||
| chr3:119417976
|
T | C | 4 | a0004c0007t0015a0004c0007t0044a0004c0007t0054others(1): Show | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1712T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 1712 | chr3 | 119417976 | |||||
| chr3:119418259
|
G | A | 1 | a0003c0006t0056 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1995G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 1995 | chr3 | 119418259 | |||||
| chr3:119418565
|
ATGTT | A | 3 | a0003c0006t0013a0003c0006t0022a0013c0020t0013 | 7 | HG01099.hp1 HG02055.hp2 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2308_*2311delTTTG | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 2308 | INFO_REALIGN_3_PRIME | chr3 | 119418565 | ||||
| chr3:119418619
|
A | G | 11 | a0001c0002t0003a0001c0004t0003a0001c0004t0010others(8): Show | 41 | HG00099.hp2 HG00741.hp2 HG01099.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2355A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 2355 | chr3 | 119418619 | |||||
| chr3:119418957
|
G | A | 6 | a0001c0001t0005a0001c0001t0007a0001c0001t0011others(3): Show | 47 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2693G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 2693 | chr3 | 119418957 | |||||
| chr3:119419007
|
C | A | 5 | a0001c0001t0025a0001c0001t0042a0001c0001t0053others(2): Show | 6 | HG00280.hp1 HG01081.hp1 HG01361.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2743C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 2743 | chr3 | 119419007 | |||||
| chr3:119419008
|
A | G | 57 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(54): Show | 239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
3_prime_UTR_variant | MODIFIER | c.*2744A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 2744 | chr3 | 119419008 | |||||
| chr3:119419065
|
C | T | 6 | a0001c0001t0005a0001c0001t0007a0001c0001t0011others(3): Show | 47 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2801C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 2801 | chr3 | 119419065 | |||||
| chr3:119419066
|
G | A | 4 | a0001c0001t0018a0001c0001t0020a0001c0001t0024others(1): Show | 10 | HG02523.hp2 HG02683.hp1 HG02970.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2802G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 2802 | chr3 | 119419066 | |||||
| chr3:119419128
|
G | C | 2 | a0001c0005t0023a0001c0005t0057 | 3 | HG02647.hp1 HG02886.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2864G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 2864 | chr3 | 119419128 | |||||
| chr3:119419277
|
G | A | 3 | a0001c0005t0014a0001c0005t0049a0001c0010t0014 | 6 | HG02280.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3013G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3013 | chr3 | 119419277 | |||||
| chr3:119419285
|
G | A | 3 | a0001c0001t0039a0001c0001t0045a0001c0001t0052 | 3 | HG02615.hp1 HG02630.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3021G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3021 | chr3 | 119419285 | |||||
| chr3:119419398
|
C | G | 1 | a0001c0001t0045 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3134C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3134 | chr3 | 119419398 | |||||
| chr3:119419564
|
A | T | 1 | a0001c0001t0053 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3300A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3300 | chr3 | 119419564 | |||||
| chr3:119419617
|
T | C | 1 | a0014c0014t0058 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3353T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3353 | chr3 | 119419617 | |||||
| chr3:119419828
|
C | T | 11 | a0001c0001t0005a0001c0001t0007a0001c0001t0011others(8): Show | 58 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*3564C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3564 | chr3 | 119419828 | |||||
| chr3:119419841
|
A | G | 1 | a0001c0004t0059 | 1 | HG01099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3577A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3577 | chr3 | 119419841 | |||||
| chr3:119419851
|
G | A | 4 | a0004c0007t0015a0004c0007t0044a0004c0007t0054others(1): Show | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3587G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3587 | chr3 | 119419851 | |||||
| chr3:119419862
|
G | A | 1 | a0001c0005t0036 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3598G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3598 | chr3 | 119419862 | |||||
| chr3:119419964
|
T | C | 5 | a0001c0001t0018a0001c0001t0020a0001c0001t0024others(2): Show | 11 | HG02523.hp2 HG02683.hp1 HG02683.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3700T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3700 | chr3 | 119419964 | |||||
| chr3:119420041
|
C | T | 1 | a0001c0001t0029 | 2 | HG03579.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3777C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3777 | chr3 | 119420041 | |||||
| chr3:119420180
|
A | G | 2 | a0001c0004t0021a0001c0004t0038 | 4 | HG02055.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3916A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3916 | chr3 | 119420180 | |||||
| chr3:119420232
|
C | T | 72 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(69): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*3968C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 3968 | chr3 | 119420232 | |||||
| chr3:119420386
|
AG | A | 4 | a0001c0001t0006a0001c0001t0008a0001c0001t0017others(1): Show | 39 | HG00323.hp1 HG00408.hp2 HG01071.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*4123delG | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 4123 | chr3 | 119420386 | |||||
| chr3:119420515
|
A | G | 1 | a0002c0003t0062 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4251A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 4251 | chr3 | 119420515 | |||||
| chr3:119420517
|
C | A | 1 | a0001c0002t0037 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4253C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 4253 | chr3 | 119420517 | |||||
| chr3:119420662
|
T | C | 5 | a0001c0001t0018a0001c0001t0020a0001c0001t0024others(2): Show | 11 | HG02523.hp2 HG02683.hp1 HG02683.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4398T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 12/12 | 4398 | chr3 | 119420662 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:119295081
|
A | T | 153 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(150): Show | 155 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.100+77A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119295081 | ||||||
| chr3:119295090
|
G | A | 1 | a0001c0001t0011g0158 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.100+86G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119295090 | ||||||
| chr3:119295140
|
CT | C | 90 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(87): Show | 90 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(87): Show |
intron_variant | MODIFIER | c.100+148delT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119295140 | |||||
| chr3:119295187
|
T | C | 6 | a0001c0005t0001g0160a0001c0005t0001g0163a0001c0005t0001g0164others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+183T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119295187 | ||||||
| chr3:119295283
|
T | A | 1 | a0010c0016t0004g0166 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.100+279T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119295283 | ||||||
| chr3:119295288
|
G | C | 7 | a0001c0005t0001g0160a0001c0005t0001g0163a0001c0005t0001g0164others(4): Show | 7 | HG02451.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+284G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119295288 | ||||||
| chr3:119295337
|
G | A | 6 | a0001c0005t0001g0160a0001c0005t0001g0163a0001c0005t0001g0164others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+333G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119295337 | ||||||
| chr3:119295385
|
G | C | 19 | a0001c0001t0020g0010a0001c0002t0001g0008a0001c0002t0001g0014others(16): Show | 19 | HG01099.hp2 HG01243.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.100+381G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119295385 | ||||||
| chr3:119295428
|
C | T | 16 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(13): Show | 16 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.100+424C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119295428 | ||||||
| chr3:119295495
|
G | C | 7 | a0001c0002t0001g0008a0001c0004t0003g0007a0001c0005t0001g0005others(4): Show | 7 | HG01496.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+491G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119295495 | ||||||
| chr3:119295516
|
G | T | 7 | a0001c0002t0001g0008a0001c0004t0003g0007a0001c0005t0001g0005others(4): Show | 7 | HG01496.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+512G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119295516 | ||||||
| chr3:119295578
|
C | A | 1 | a0002c0003t0009g0167 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.100+574C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119295578 | ||||||
| chr3:119295630
|
T | C | 5 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0002t0001g0023others(2): Show | 5 | HG01255.hp2 HG01975.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+626T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119295630 | ||||||
| chr3:119295665
|
T | C | 1 | a0001c0001t0020g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.100+661T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119295665 | ||||||
| chr3:119295688
|
T | G | 1 | a0001c0001t0060g0026 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.100+684T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119295688 | ||||||
| chr3:119295690
|
C | G | 218 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(215): Show | 220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.100+686C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119295690 | ||||||
| chr3:119295700
|
T | C | 16 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(13): Show | 16 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.100+696T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119295700 | ||||||
| chr3:119295772
|
G | A | 1 | a0002c0003t0002g0086 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100+768G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119295772 | ||||||
| chr3:119295776
|
G | A | 1 | a0001c0002t0012g0174 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.100+772G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119295776 | ||||||
| chr3:119296183
|
G | A | 1 | a0001c0001t0017g0175 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.100+1179G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119296183 | ||||||
| chr3:119296274
|
A | G | 10 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(7): Show | 10 | HG02083.hp1 HG02129.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+1270A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119296274 | ||||||
| chr3:119296588
|
G | A | 10 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(7): Show | 10 | HG02083.hp1 HG02129.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+1584G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119296588 | ||||||
| chr3:119296596
|
T | G | 16 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(13): Show | 16 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.100+1592T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119296596 | ||||||
| chr3:119296752
|
C | CA | 7 | a0001c0002t0001g0008a0001c0004t0003g0007a0001c0005t0001g0005others(4): Show | 7 | HG01496.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+1757dupA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119296752 | |||||
| chr3:119296826
|
A | G | 12 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(9): Show | 12 | HG02055.hp1 HG02145.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.100+1822A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119296826 | ||||||
| chr3:119296860
|
G | A | 1 | a0014c0014t0058g0003 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.100+1856G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119296860 | ||||||
| chr3:119297061
|
G | A | 1 | a0001c0004t0010g0176 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.100+2057G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119297061 | ||||||
| chr3:119297191
|
G | T | 1 | a0001c0001t0008g0299 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.100+2187G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119297191 | ||||||
| chr3:119297236
|
T | A | 1 | a0001c0001t0005g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.100+2232T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119297236 | ||||||
| chr3:119297271
|
T | G | 7 | a0001c0002t0001g0008a0001c0004t0003g0007a0001c0005t0001g0005others(4): Show | 7 | HG01496.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+2267T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119297271 | ||||||
| chr3:119297286
|
C | T | 22 | a0001c0001t0020g0056a0001c0001t0060g0026a0001c0001t0061g0057others(19): Show | 22 | HG01099.hp2 HG01243.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.100+2282C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119297286 | ||||||
| chr3:119297314
|
C | T | 7 | a0001c0002t0001g0008a0001c0004t0003g0007a0001c0005t0001g0005others(4): Show | 7 | HG01496.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+2310C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119297314 | ||||||
| chr3:119297351
|
A | C | 22 | a0001c0001t0020g0056a0001c0001t0060g0026a0001c0001t0061g0057others(19): Show | 22 | HG01099.hp2 HG01243.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.100+2347A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119297351 | ||||||
| chr3:119297381
|
T | A | 10 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(7): Show | 10 | HG02083.hp1 HG02129.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+2377T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119297381 | ||||||
| chr3:119297448
|
C | T | 4 | a0001c0001t0007g0296a0002c0003t0009g0297a0002c0003t0009g0298others(1): Show | 4 | HG00738.hp1 HG00741.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+2444C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119297448 | ||||||
| chr3:119297513
|
G | GAC | 228 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(225): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.100+2510_100+2511i others(4): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119297513 | |||||
| chr3:119297559
|
A | C | 2 | a0002c0003t0009g0297a0002c0003t0009g0298 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.100+2555A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119297559 | ||||||
| chr3:119297615
|
T | C | 15 | a0001c0001t0020g0056a0001c0001t0060g0026a0001c0001t0061g0057others(12): Show | 15 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.100+2611T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119297615 | ||||||
| chr3:119297734
|
A | G | 228 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(225): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.100+2730A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119297734 | ||||||
| chr3:119297780
|
G | A | 10 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(7): Show | 10 | HG02055.hp1 HG03017.hp2 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.100+2776G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119297780 | ||||||
| chr3:119297909
|
A | AAC | 95 | a0001c0001t0005g0087a0001c0001t0005g0278a0001c0001t0007g0225others(92): Show | 96 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.100+2940_100+2941d others(4): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119297909 | |||||
| chr3:119297909
|
A | AACAC | 39 | a0001c0001t0007g0202a0001c0001t0008g0192a0001c0001t0008g0199others(36): Show | 40 | HG00280.hp2 HG00735.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.100+2938_100+2941d others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119297909 | |||||
| chr3:119297909
|
A | AACACAC | 5 | a0001c0001t0008g0178a0001c0001t0008g0180a0001c0001t0050g0177others(2): Show | 5 | HG02683.hp2 HG02976.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+2936_100+2941d others(8): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119297909 | |||||
| chr3:119297909
|
A | AACACACA others(3): Show |
2 | a0001c0005t0001g0019a0001c0005t0001g0020 | 2 | HG02647.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.100+2932_100+2941d others(12): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119297909 | |||||
| chr3:119297909
|
A | AACACACA others(7): Show |
4 | a0001c0001t0060g0026a0001c0002t0028g0017a0001c0002t0028g0018others(1): Show | 4 | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+2928_100+2941d others(16): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119297909 | |||||
| chr3:119297909
|
A | AACACACA others(9): Show |
4 | a0001c0001t0061g0057a0001c0002t0001g0014a0001c0004t0059g0015others(1): Show | 4 | HG01099.hp2 HG02486.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+2926_100+2941d others(18): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119297909 | |||||
| chr3:119297909
|
A | AACACACA others(11): Show |
2 | a0001c0005t0001g0012a0006c0011t0015g0013 | 2 | HG01243.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.100+2924_100+2941d others(20): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119297909 | |||||
| chr3:119297909
|
A | AACACACA others(15): Show |
2 | a0001c0001t0020g0056a0001c0004t0021g0055 | 2 | HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.100+2920_100+2941d others(24): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119297909 | |||||
| chr3:119297909
|
A | AACACACA others(17): Show |
1 | a0003c0006t0056g0011 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.100+2918_100+2941d others(26): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119297909 | |||||
| chr3:119297909
|
A | C | 1 | a0001c0001t0011g0292 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.100+2905A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119297909 | ||||||
| chr3:119297909
|
AAC | A | 15 | a0001c0001t0005g0156a0001c0001t0005g0172a0001c0001t0017g0175others(12): Show | 15 | HG02083.hp1 HG02523.hp1 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.100+2940_100+2941d others(4): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119297909 | |||||
| chr3:119297909
|
AACAC | A | 12 | a0001c0001t0006g0065a0001c0001t0006g0066a0001c0001t0029g0054others(9): Show | 12 | HG01496.hp1 HG02258.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.100+2938_100+2941d others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119297909 | |||||
| chr3:119297909
|
AACACACA others(11): Show |
A | 6 | a0001c0005t0001g0160a0001c0005t0001g0163a0001c0005t0001g0164others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+2924_100+2941d others(20): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119297909 | |||||
| chr3:119298029
|
G | T | 10 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(7): Show | 10 | HG02083.hp1 HG02129.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+3025G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119298029 | ||||||
| chr3:119298417
|
C | T | 5 | a0001c0001t0042g0282a0001c0005t0001g0163a0001c0005t0001g0164others(2): Show | 5 | HG00280.hp1 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+3413C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119298417 | ||||||
| chr3:119298525
|
A | T | 7 | a0001c0002t0012g0174a0001c0005t0001g0160a0001c0005t0001g0163others(4): Show | 7 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+3521A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119298525 | ||||||
| chr3:119298535
|
A | T | 58 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(55): Show | 58 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(55): Show |
intron_variant | MODIFIER | c.100+3531A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119298535 | ||||||
| chr3:119298688
|
C | T | 1 | a0001c0001t0020g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.100+3684C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119298688 | ||||||
| chr3:119298849
|
A | G | 3 | a0001c0001t0020g0056a0001c0001t0060g0026a0001c0001t0061g0057 | 3 | HG02486.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.100+3845A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119298849 | ||||||
| chr3:119298851
|
A | G | 22 | a0001c0001t0020g0056a0001c0001t0060g0026a0001c0001t0061g0057others(19): Show | 22 | HG01099.hp2 HG01243.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.100+3847A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119298851 | ||||||
| chr3:119298859
|
G | C | 126 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(123): Show | 127 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(124): Show |
intron_variant | MODIFIER | c.100+3855G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119298859 | ||||||
| chr3:119299067
|
G | A | 7 | a0001c0002t0012g0174a0001c0005t0001g0160a0001c0005t0001g0163others(4): Show | 7 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+4063G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119299067 | ||||||
| chr3:119299166
|
GA | G | 15 | a0001c0001t0020g0056a0001c0001t0060g0026a0001c0001t0061g0057others(12): Show | 15 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.100+4169delA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119299166 | |||||
| chr3:119299176
|
C | G | 15 | a0001c0001t0020g0056a0001c0001t0060g0026a0001c0001t0061g0057others(12): Show | 15 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.100+4172C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119299176 | ||||||
| chr3:119299199
|
A | G | 1 | a0001c0001t0008g0281 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.100+4195A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119299199 | ||||||
| chr3:119299256
|
T | A | 1 | a0002c0003t0043g0210 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.100+4252T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119299256 | ||||||
| chr3:119299309
|
C | T | 6 | a0001c0005t0001g0160a0001c0005t0001g0163a0001c0005t0001g0164others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+4305C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119299309 | ||||||
| chr3:119299419
|
C | A | 1 | a0001c0001t0011g0300 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.100+4415C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119299419 | ||||||
| chr3:119299550
|
G | A | 1 | a0001c0005t0001g0029 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.100+4546G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119299550 | ||||||
| chr3:119299579
|
C | G | 15 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(12): Show | 15 | HG02055.hp1 HG02145.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.100+4575C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119299579 | ||||||
| chr3:119299597
|
A | G | 2 | a0001c0001t0006g0154a0011c0019t0005g0155 | 2 | NA18981.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.100+4593A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119299597 | ||||||
| chr3:119299659
|
A | G | 15 | a0001c0001t0020g0056a0001c0001t0060g0026a0001c0001t0061g0057others(12): Show | 15 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.100+4655A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119299659 | ||||||
| chr3:119299772
|
A | C | 3 | a0001c0001t0029g0054a0002c0003t0030g0053a0013c0020t0013g0051 | 3 | HG03041.hp2 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.100+4768A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119299772 | ||||||
| chr3:119299782
|
C | A | 12 | a0001c0001t0020g0056a0001c0001t0060g0026a0001c0001t0061g0057others(9): Show | 12 | HG01496.hp1 HG01884.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.100+4778C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119299782 | ||||||
| chr3:119299847
|
A | C | 15 | a0001c0001t0020g0056a0001c0001t0060g0026a0001c0001t0061g0057others(12): Show | 15 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.100+4843A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119299847 | ||||||
| chr3:119299907
|
G | A | 7 | a0001c0002t0001g0008a0001c0004t0003g0007a0001c0005t0001g0005others(4): Show | 7 | HG01496.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+4903G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119299907 | ||||||
| chr3:119300026
|
C | G | 2 | a0001c0001t0020g0064a0002c0003t0002g0063 | 2 | HG03239.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.100+5022C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300026 | ||||||
| chr3:119300112
|
C | T | 4 | a0001c0001t0020g0056a0001c0001t0060g0026a0001c0001t0061g0057others(1): Show | 4 | HG02486.hp1 HG03130.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+5108C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300112 | ||||||
| chr3:119300202
|
G | A | 1 | a0003c0006t0056g0011 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.100+5198G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300202 | ||||||
| chr3:119300262
|
T | C | 7 | a0001c0002t0001g0008a0001c0004t0003g0007a0001c0005t0001g0005others(4): Show | 7 | HG01496.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+5258T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300262 | ||||||
| chr3:119300289
|
G | C | 19 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(16): Show | 19 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.100+5285G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300289 | ||||||
| chr3:119300489
|
A | G | 1 | a0001c0005t0001g0049 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.100+5485A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300489 | ||||||
| chr3:119300567
|
G | A | 5 | a0001c0001t0020g0056a0001c0001t0060g0026a0001c0001t0061g0057others(2): Show | 5 | HG01884.hp2 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+5563G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300567 | ||||||
| chr3:119300616
|
G | C | 2 | a0001c0005t0001g0190a0001c0005t0001g0191 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.100+5612G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300616 | ||||||
| chr3:119300621
|
A | G | 31 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(28): Show | 31 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.100+5617A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300621 | ||||||
| chr3:119300684
|
T | C | 3 | a0001c0001t0008g0212a0001c0001t0008g0213a0001c0002t0004g0211 | 3 | HG00408.hp2 HG02056.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.100+5680T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300684 | ||||||
| chr3:119300702
|
C | G | 4 | a0001c0001t0018g0207a0001c0001t0018g0208a0001c0001t0018g0209others(1): Show | 4 | HG02683.hp2 HG03654.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+5698C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300702 | ||||||
| chr3:119300742
|
G | T | 10 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(7): Show | 10 | HG02083.hp1 HG02129.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+5738G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300742 | ||||||
| chr3:119300751
|
T | C | 126 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(123): Show | 127 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(124): Show |
intron_variant | MODIFIER | c.100+5747T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300751 | ||||||
| chr3:119300758
|
C | T | 26 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0020g0043others(23): Show | 26 | HG00639.hp1 HG01106.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.100+5754C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300758 | ||||||
| chr3:119300792
|
A | T | 1 | a0001c0001t0006g0025 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.100+5788A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300792 | ||||||
| chr3:119300842
|
A | AAAAG | 15 | a0001c0001t0006g0092a0001c0001t0007g0296a0001c0001t0008g0192others(12): Show | 15 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.100+5868_100+5871d others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119300842 | |||||
| chr3:119300842
|
A | G | 5 | a0001c0001t0005g0278a0001c0001t0008g0277a0001c0002t0016g0279others(2): Show | 6 | HG02080.hp1 HG02155.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+5838A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300842 | ||||||
| chr3:119300842
|
AAAAG | A | 70 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0006g0025others(67): Show | 70 | HG00639.hp1 HG01099.hp2 HG01106.hp2 others(67): Show |
intron_variant | MODIFIER | c.100+5868_100+5871d others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119300842 | |||||
| chr3:119300842
|
AAAAGAAA others(1): Show |
A | 32 | a0001c0001t0006g0148a0001c0001t0007g0275a0001c0001t0007g0276others(29): Show | 33 | HG00323.hp1 HG00735.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.100+5864_100+5871d others(10): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119300842 | |||||
| chr3:119300842
|
AAAAGAAA others(5): Show |
A | 6 | a0001c0001t0005g0153a0001c0001t0050g0177a0001c0004t0003g0150others(3): Show | 6 | HG02683.hp2 HG02698.hp1 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+5860_100+5871d others(14): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119300842 | |||||
| chr3:119300845
|
AG | A | 9 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(6): Show | 9 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+5842delG | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300845 | ||||||
| chr3:119300845
|
AGAAAG | A | 16 | a0001c0001t0020g0056a0001c0001t0060g0026a0001c0001t0061g0057others(13): Show | 16 | HG01496.hp1 HG01884.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.100+5842_100+5846d others(7): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300845 | ||||||
| chr3:119300846
|
G | A | 3 | a0001c0001t0029g0054a0002c0003t0030g0053a0013c0020t0013g0051 | 3 | HG03041.hp2 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.100+5842G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300846 | ||||||
| chr3:119300850
|
G | A | 1 | a0001c0005t0001g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.100+5846G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300850 | ||||||
| chr3:119300854
|
G | A | 7 | a0001c0002t0001g0008a0001c0004t0003g0007a0001c0005t0001g0005others(4): Show | 7 | HG01496.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+5850G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300854 | ||||||
| chr3:119300957
|
C | T | 1 | a0002c0003t0009g0268 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.100+5953C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119300957 | ||||||
| chr3:119301091
|
C | G | 7 | a0001c0002t0001g0008a0001c0004t0003g0007a0001c0005t0001g0005others(4): Show | 7 | HG01496.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+6087C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119301091 | ||||||
| chr3:119301216
|
C | T | 6 | a0001c0005t0001g0160a0001c0005t0001g0163a0001c0005t0001g0164others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+6212C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119301216 | ||||||
| chr3:119301223
|
C | A | 7 | a0001c0001t0020g0010a0001c0005t0001g0160a0001c0005t0001g0163others(4): Show | 7 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+6219C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119301223 | ||||||
| chr3:119301233
|
C | T | 1 | a0001c0004t0010g0267 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.100+6229C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119301233 | ||||||
| chr3:119301234
|
G | A | 3 | a0001c0001t0029g0054a0002c0003t0030g0053a0013c0020t0013g0051 | 3 | HG03041.hp2 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.100+6230G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119301234 | ||||||
| chr3:119301356
|
G | A | 7 | a0001c0002t0001g0008a0001c0004t0003g0007a0001c0005t0001g0005others(4): Show | 7 | HG01496.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+6352G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119301356 | ||||||
| chr3:119301443
|
G | A | 3 | a0001c0001t0029g0054a0002c0003t0030g0053a0013c0020t0013g0051 | 3 | HG03041.hp2 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.100+6439G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119301443 | ||||||
| chr3:119301477
|
G | GT | 8 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0005t0012g0285others(5): Show | 8 | HG00639.hp1 HG01106.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+6478dupT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119301477 | |||||
| chr3:119301578
|
A | C | 102 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(99): Show | 103 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.100+6574A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119301578 | ||||||
| chr3:119301605
|
T | C | 16 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(13): Show | 16 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.100+6601T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119301605 | ||||||
| chr3:119301628
|
A | G | 124 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(121): Show | 125 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(122): Show |
intron_variant | MODIFIER | c.100+6624A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119301628 | ||||||
| chr3:119301644
|
GT | G | 118 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(115): Show | 119 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(116): Show |
intron_variant | MODIFIER | c.100+6649delT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119301644 | |||||
| chr3:119301653
|
T | A | 6 | a0001c0005t0001g0160a0001c0005t0001g0163a0001c0005t0001g0164others(3): Show | 6 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+6649T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119301653 | ||||||
| chr3:119301910
|
G | A | 7 | a0001c0002t0001g0008a0001c0004t0003g0007a0001c0005t0001g0005others(4): Show | 7 | HG01496.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+6906G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119301910 | ||||||
| chr3:119301929
|
T | C | 1 | a0001c0001t0005g0168 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.100+6925T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119301929 | ||||||
| chr3:119301992
|
G | T | 15 | a0001c0001t0020g0056a0001c0001t0029g0054a0001c0001t0060g0026others(12): Show | 15 | HG01496.hp1 HG01884.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.100+6988G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119301992 | ||||||
| chr3:119302167
|
C | A | 1 | a0001c0001t0020g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.100+7163C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119302167 | ||||||
| chr3:119302169
|
G | A | 1 | a0002c0003t0062g0093 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.100+7165G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119302169 | ||||||
| chr3:119302223
|
T | C | 92 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(89): Show | 93 | HG00099.hp1 HG00323.hp2 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.100+7219T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119302223 | ||||||
| chr3:119302377
|
T | C | 4 | a0001c0001t0018g0207a0001c0001t0018g0208a0001c0001t0018g0209others(1): Show | 4 | HG02683.hp2 HG03654.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+7373T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119302377 | ||||||
| chr3:119302536
|
T | C | 1 | a0001c0001t0020g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.100+7532T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119302536 | ||||||
| chr3:119302682
|
G | A | 8 | a0001c0001t0020g0056a0001c0001t0029g0054a0001c0001t0060g0026others(5): Show | 8 | HG01884.hp2 HG02486.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.100+7678G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119302682 | ||||||
| chr3:119302760
|
A | G | 1 | a0001c0001t0011g0158 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.100+7756A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119302760 | ||||||
| chr3:119303044
|
G | C | 7 | a0001c0002t0001g0008a0001c0004t0003g0007a0001c0005t0001g0005others(4): Show | 7 | HG01496.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+8040G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303044 | ||||||
| chr3:119303060
|
A | C | 77 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(74): Show | 78 | HG00099.hp1 HG00323.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.100+8056A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303060 | ||||||
| chr3:119303244
|
C | T | 6 | a0001c0002t0001g0008a0001c0004t0003g0007a0001c0005t0001g0005others(3): Show | 6 | HG01496.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+8240C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303244 | ||||||
| chr3:119303285
|
G | A | 1 | a0001c0004t0010g0219 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.100+8281G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303285 | ||||||
| chr3:119303301
|
A | G | 2 | a0001c0001t0005g0077a0001c0001t0005g0078 | 2 | HG00099.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.100+8297A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303301 | ||||||
| chr3:119303428
|
A | G | 8 | a0001c0001t0020g0056a0001c0001t0029g0054a0001c0001t0060g0026others(5): Show | 8 | HG01884.hp2 HG02486.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.100+8424A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303428 | ||||||
| chr3:119303608
|
G | A | 1 | a0002c0003t0009g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.100+8604G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303608 | ||||||
| chr3:119303628
|
C | T | 26 | a0001c0001t0011g0001a0001c0001t0011g0158a0001c0001t0011g0183others(23): Show | 27 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.100+8624C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303628 | ||||||
| chr3:119303688
|
A | C | 1 | a0001c0002t0012g0174 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.100+8684A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303688 | ||||||
| chr3:119303692
|
C | T | 27 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0020g0043others(24): Show | 27 | HG00639.hp1 HG01106.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.100+8688C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303692 | ||||||
| chr3:119303700
|
C | G | 1 | a0001c0002t0001g0084 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.100+8696C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303700 | ||||||
| chr3:119303782
|
G | GT | 14 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(11): Show | 14 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.100+8784dupT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119303782 | |||||
| chr3:119303788
|
TG | T | 92 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0006g0025others(89): Show | 93 | HG00639.hp1 HG00735.hp1 HG01071.hp1 others(90): Show |
intron_variant | MODIFIER | c.100+8785delG | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303788 | ||||||
| chr3:119303788
|
TGTTGTTG others(6): Show |
T | 10 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(7): Show | 10 | HG02083.hp1 HG02129.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+8785_100+8797d others(15): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303788 | ||||||
| chr3:119303789
|
G | T | 19 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(16): Show | 19 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.100+8785G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303789 | ||||||
| chr3:119303792
|
G | T | 67 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(64): Show | 68 | HG00099.hp1 HG00323.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.100+8788G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303792 | ||||||
| chr3:119303795
|
G | T | 8 | a0001c0002t0001g0014a0001c0002t0028g0017a0001c0002t0028g0018others(5): Show | 8 | HG01099.hp2 HG01243.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.100+8791G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303795 | ||||||
| chr3:119303826
|
G | A | 1 | a0001c0001t0024g0221 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.100+8822G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303826 | ||||||
| chr3:119303833
|
C | T | 1 | a0001c0001t0011g0292 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.100+8829C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303833 | ||||||
| chr3:119303997
|
T | C | 10 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(7): Show | 10 | HG02083.hp1 HG02129.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+8993T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119303997 | ||||||
| chr3:119304028
|
T | G | 1 | a0001c0002t0012g0174 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.100+9024T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119304028 | ||||||
| chr3:119304303
|
G | A | 2 | a0001c0001t0006g0094a0001c0004t0003g0095 | 2 | NA18994.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.100+9299G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119304303 | ||||||
| chr3:119304398
|
A | G | 2 | a0001c0005t0001g0190a0001c0005t0001g0191 | 2 | HG03041.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.100+9394A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119304398 | ||||||
| chr3:119304499
|
G | A | 34 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0020g0043others(31): Show | 34 | HG00639.hp1 HG01106.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.100+9495G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119304499 | ||||||
| chr3:119304546
|
A | G | 34 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0020g0043others(31): Show | 34 | HG00639.hp1 HG01106.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.100+9542A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119304546 | ||||||
| chr3:119304591
|
A | G | 124 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(121): Show | 125 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(122): Show |
intron_variant | MODIFIER | c.100+9587A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119304591 | ||||||
| chr3:119304657
|
GATAA | G | 34 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0020g0043others(31): Show | 34 | HG00639.hp1 HG01106.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.100+9654_100+9657d others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119304657 | ||||||
| chr3:119304705
|
T | C | 1 | a0004c0007t0015g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.100+9701T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119304705 | ||||||
| chr3:119304768
|
G | A | 1 | a0001c0004t0010g0267 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.100+9764G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119304768 | ||||||
| chr3:119304801
|
G | A | 1 | a0001c0001t0008g0277 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.100+9797G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119304801 | ||||||
| chr3:119304894
|
C | CAAAAT | 4 | a0001c0002t0004g0266a0002c0003t0002g0145a0002c0003t0002g0146others(1): Show | 4 | HG01106.hp1 HG03195.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+9935_100+9939d others(7): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119304894 | |||||
| chr3:119304894
|
CAAAAT | C | 71 | a0001c0001t0005g0278a0001c0001t0007g0225a0001c0001t0007g0226others(68): Show | 72 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.100+9935_100+9939d others(7): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119304894 | |||||
| chr3:119304894
|
CAAAATAA others(8): Show |
C | 1 | a0001c0001t0005g0096 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.100+9925_100+9939d others(17): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119304894 | |||||
| chr3:119304894
|
CAAAATAA others(13): Show |
C | 125 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(122): Show | 126 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.100+9920_100+9939d others(22): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119304894 | |||||
| chr3:119304956
|
G | T | 1 | a0002c0003t0009g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.100+9952G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119304956 | ||||||
| chr3:119304957
|
G | A | 124 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(121): Show | 125 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(122): Show |
intron_variant | MODIFIER | c.100+9953G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119304957 | ||||||
| chr3:119305033
|
A | G | 10 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(7): Show | 10 | HG02083.hp1 HG02129.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+10029A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119305033 | ||||||
| chr3:119305124
|
C | T | 124 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(121): Show | 125 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(122): Show |
intron_variant | MODIFIER | c.100+10120C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119305124 | ||||||
| chr3:119305137
|
C | T | 1 | a0001c0002t0012g0174 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.100+10133C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119305137 | ||||||
| chr3:119305170
|
C | T | 1 | a0001c0002t0004g0246 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.100+10166C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119305170 | ||||||
| chr3:119305295
|
C | T | 8 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0005t0012g0285others(5): Show | 8 | HG00639.hp1 HG01106.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+10291C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119305295 | ||||||
| chr3:119305332
|
G | A | 1 | a0004c0007t0015g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.100+10328G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119305332 | ||||||
| chr3:119305415
|
A | G | 1 | a0002c0003t0002g0082 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.100+10411A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119305415 | ||||||
| chr3:119305532
|
G | A | 101 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(98): Show | 102 | HG00099.hp1 HG00323.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.100+10528G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119305532 | ||||||
| chr3:119305735
|
C | A | 1 | a0002c0003t0009g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.100+10731C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119305735 | ||||||
| chr3:119305914
|
G | A | 1 | a0001c0001t0020g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.100+10910G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119305914 | ||||||
| chr3:119305989
|
C | A | 6 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0005t0012g0285others(3): Show | 6 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+10985C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119305989 | ||||||
| chr3:119306090
|
C | T | 76 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(73): Show | 77 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(74): Show |
intron_variant | MODIFIER | c.100+11086C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119306090 | ||||||
| chr3:119306171
|
A | G | 90 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(87): Show | 91 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.100+11167A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119306171 | ||||||
| chr3:119306411
|
G | C | 22 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(19): Show | 22 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.100+11407G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119306411 | ||||||
| chr3:119306465
|
G | A | 29 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0020g0043others(26): Show | 29 | HG01255.hp2 HG01496.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.100+11461G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119306465 | ||||||
| chr3:119306498
|
A | C | 1 | a0002c0003t0009g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.100+11494A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119306498 | ||||||
| chr3:119306539
|
G | A | 3 | a0001c0002t0016g0097a0001c0002t0016g0098a0001c0002t0016g0099 | 3 | NA18953.hp2 NA18998.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.100+11535G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119306539 | ||||||
| chr3:119306889
|
A | G | 1 | a0001c0001t0020g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.100+11885A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119306889 | ||||||
| chr3:119306953
|
T | G | 137 | a0001c0001t0005g0022a0001c0001t0005g0278a0001c0001t0006g0025others(134): Show | 138 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.100+11949T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119306953 | ||||||
| chr3:119306980
|
G | A | 137 | a0001c0001t0005g0022a0001c0001t0005g0278a0001c0001t0006g0025others(134): Show | 138 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.100+11976G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119306980 | ||||||
| chr3:119307020
|
G | GA | 9 | a0001c0001t0020g0056a0001c0001t0060g0026a0001c0001t0061g0057others(6): Show | 9 | HG01884.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.100+12026dupA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307020 | |||||
| chr3:119307034
|
A | C | 33 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0011g0300others(30): Show | 33 | HG01255.hp2 HG01884.hp2 HG01975.hp2 others(30): Show |
intron_variant | MODIFIER | c.100+12030A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119307034 | ||||||
| chr3:119307043
|
G | GT | 141 | a0001c0001t0005g0022a0001c0001t0005g0278a0001c0001t0006g0025others(138): Show | 142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.100+12049dupT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307043 | |||||
| chr3:119307043
|
G | GTT | 6 | a0001c0001t0045g0286a0001c0005t0012g0285a0001c0005t0012g0287others(3): Show | 6 | HG00639.hp1 HG01106.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+12048_100+1204 others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307043 | |||||
| chr3:119307097
|
C | T | 1 | a0001c0004t0032g0071 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.100+12093C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119307097 | ||||||
| chr3:119307231
|
C | A | 3 | a0001c0002t0004g0247a0002c0003t0009g0220a0010c0016t0004g0166 | 3 | HG00735.hp2 HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.100+12227C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119307231 | ||||||
| chr3:119307520
|
C | T | 1 | a0003c0006t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.100+12516C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119307520 | ||||||
| chr3:119307546
|
A | T | 21 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(18): Show | 21 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.100+12542A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119307546 | ||||||
| chr3:119307826
|
C | G | 1 | a0004c0007t0015g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.100+12822C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119307826 | ||||||
| chr3:119307939
|
G | GAAAAAAA others(5): Show |
1 | a0004c0007t0015g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.100+12935_100+1293 others(16): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119307939 | ||||||
| chr3:119307940
|
C | A | 1 | a0004c0007t0015g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.100+12936C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119307940 | ||||||
| chr3:119307940
|
C | CAAAAA | 103 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0007g0202others(100): Show | 104 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.100+12952_100+1295 others(9): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119307940
|
C | CAAAAAA | 28 | a0001c0001t0005g0278a0001c0001t0007g0225a0001c0001t0007g0226others(25): Show | 28 | HG00621.hp1 HG00741.hp1 HG01256.hp2 others(25): Show |
intron_variant | MODIFIER | c.100+12951_100+1295 others(10): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119307940
|
C | CAAAAAAA | 12 | a0001c0001t0008g0178a0001c0001t0020g0010a0001c0001t0025g0223others(9): Show | 12 | HG00639.hp1 HG00735.hp2 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.100+12950_100+1295 others(11): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119307940
|
C | CAAAAAAA others(1): Show |
6 | a0001c0001t0006g0092a0001c0002t0016g0133a0001c0005t0001g0164others(3): Show | 6 | HG00438.hp2 HG02523.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+12949_100+1295 others(12): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119307940
|
C | CAAAAAAA others(2): Show |
20 | a0001c0001t0011g0001a0001c0001t0011g0158a0001c0001t0011g0184others(17): Show | 21 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.100+12948_100+1295 others(13): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119307940
|
C | CAAAAAAA others(3): Show |
26 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(23): Show | 26 | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.100+12947_100+1295 others(14): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119307940
|
C | CAAAAAAA others(4): Show |
7 | a0001c0001t0029g0054a0001c0002t0001g0084a0001c0002t0012g0174others(4): Show | 7 | HG00621.hp2 HG02257.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+12946_100+1295 others(15): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119307940
|
C | CAAAAAAA others(5): Show |
2 | a0001c0004t0010g0244a0002c0003t0030g0053 | 2 | HG03041.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.100+12945_100+1295 others(16): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119307940
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0018g0207a0001c0001t0018g0208 | 2 | HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.100+12940_100+1295 others(21): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119307940
|
C | CAAAAAAA others(11): Show |
4 | a0001c0001t0018g0209a0001c0005t0001g0160a0001c0005t0001g0163others(1): Show | 4 | HG02572.hp1 HG02622.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+12939_100+1295 others(22): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119307940
|
C | CAAAAAAA others(12): Show |
3 | a0001c0001t0006g0065a0001c0001t0006g0066a0001c0004t0064g0061 | 3 | HG03491.hp2 HG03492.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.100+12938_100+1295 others(23): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119307940
|
C | CAAAAAAA others(13): Show |
32 | a0001c0001t0005g0096a0001c0001t0005g0129a0001c0001t0005g0168others(29): Show | 32 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.100+12937_100+1295 others(24): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119307940
|
C | CAAAAAAA others(14): Show |
22 | a0001c0001t0005g0058a0001c0001t0005g0117a0001c0001t0005g0121others(19): Show | 22 | HG00597.hp2 HG00741.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.100+12956_100+1295 others(25): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119307940
|
C | CAAAAAAA others(15): Show |
11 | a0001c0001t0005g0111a0001c0001t0006g0102a0001c0001t0006g0103others(8): Show | 11 | HG01243.hp1 HG02293.hp2 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.100+12956_100+1295 others(26): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119307940
|
C | CAAAAAAA others(16): Show |
1 | a0001c0002t0001g0101 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.100+12956_100+1295 others(27): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119307940
|
C | CAAAAAAA others(17): Show |
2 | a0001c0001t0007g0293a0002c0003t0026g0294 | 2 | HG00639.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.100+12956_100+1295 others(28): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119307940
|
C | CAAAAAAA others(18): Show |
2 | a0001c0001t0006g0100a0002c0003t0031g0089 | 2 | HG01167.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.100+12956_100+1295 others(29): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119307940
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0006g0154 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.100+12956_100+1295 others(31): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119307940
|
C | CAAAAAAA others(23): Show |
1 | a0001c0001t0005g0169 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.100+12956_100+1295 others(34): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119307940 | |||||
| chr3:119308027
|
G | A | 11 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(8): Show | 11 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.100+13023G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119308027 | ||||||
| chr3:119308042
|
A | G | 100 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(97): Show | 101 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.100+13038A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119308042 | ||||||
| chr3:119308148
|
G | A | 1 | a0001c0001t0006g0073 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.100+13144G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119308148 | ||||||
| chr3:119308328
|
C | T | 7 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0005t0012g0285others(4): Show | 7 | HG00639.hp1 HG01106.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+13324C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119308328 | ||||||
| chr3:119308497
|
A | G | 137 | a0001c0001t0005g0022a0001c0001t0005g0278a0001c0001t0006g0025others(134): Show | 138 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.100+13493A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119308497 | ||||||
| chr3:119308532
|
C | T | 2 | a0001c0002t0004g0247a0002c0003t0009g0220 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.100+13528C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119308532 | ||||||
| chr3:119308556
|
G | T | 4 | a0001c0005t0001g0160a0001c0005t0001g0163a0001c0005t0001g0164others(1): Show | 4 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+13552G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119308556 | ||||||
| chr3:119308628
|
T | C | 137 | a0001c0001t0005g0022a0001c0001t0005g0278a0001c0001t0006g0025others(134): Show | 138 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.100+13624T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119308628 | ||||||
| chr3:119308914
|
C | T | 4 | a0001c0005t0001g0160a0001c0005t0001g0163a0001c0005t0001g0164others(1): Show | 4 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+13910C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119308914 | ||||||
| chr3:119308957
|
C | T | 2 | a0001c0001t0020g0010a0003c0006t0001g0159 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.100+13953C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119308957 | ||||||
| chr3:119309075
|
C | T | 21 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(18): Show | 21 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.100+14071C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119309075 | ||||||
| chr3:119309192
|
T | G | 32 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0011g0300others(29): Show | 32 | HG01255.hp2 HG01884.hp2 HG01975.hp2 others(29): Show |
intron_variant | MODIFIER | c.100+14188T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119309192 | ||||||
| chr3:119309268
|
G | T | 1 | a0001c0002t0012g0206 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100+14264G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119309268 | ||||||
| chr3:119309387
|
G | A | 3 | a0001c0001t0007g0250a0001c0001t0007g0272a0001c0001t0008g0299 | 3 | NA18957.hp2 NA18981.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.100+14383G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119309387 | ||||||
| chr3:119309457
|
C | T | 4 | a0001c0005t0001g0005a0001c0005t0001g0165a0001c0010t0014g0004others(1): Show | 4 | HG02280.hp2 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+14453C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119309457 | ||||||
| chr3:119309591
|
CA | C | 100 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(97): Show | 101 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.100+14598delA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119309591 | |||||
| chr3:119309718
|
C | A | 1 | a0002c0003t0002g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.100+14714C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119309718 | ||||||
| chr3:119309731
|
G | C | 7 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0005t0012g0285others(4): Show | 7 | HG00639.hp1 HG01106.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+14727G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119309731 | ||||||
| chr3:119309747
|
G | A | 3 | a0001c0001t0008g0212a0001c0001t0008g0213a0001c0002t0004g0211 | 3 | HG00408.hp2 HG02056.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.100+14743G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119309747 | ||||||
| chr3:119309814
|
C | T | 33 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0011g0300others(30): Show | 33 | HG01255.hp2 HG01884.hp2 HG01975.hp2 others(30): Show |
intron_variant | MODIFIER | c.100+14810C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119309814 | ||||||
| chr3:119309875
|
C | T | 1 | a0001c0001t0005g0142 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.100+14871C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119309875 | ||||||
| chr3:119309937
|
G | A | 3 | a0001c0001t0008g0212a0001c0001t0008g0213a0001c0002t0004g0211 | 3 | HG00408.hp2 HG02056.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.100+14933G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119309937 | ||||||
| chr3:119309949
|
G | GT | 104 | a0001c0001t0005g0156a0001c0001t0005g0278a0001c0001t0007g0202others(101): Show | 105 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.100+14960dupT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119309949 | |||||
| chr3:119309949
|
GT | G | 28 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0065others(25): Show | 28 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.100+14960delT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119309949 | |||||
| chr3:119310180
|
G | A | 4 | a0001c0005t0001g0160a0001c0005t0001g0163a0001c0005t0001g0164others(1): Show | 4 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+15176G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119310180 | ||||||
| chr3:119310374
|
T | C | 1 | a0001c0001t0024g0221 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.100+15370T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119310374 | ||||||
| chr3:119310575
|
G | A | 2 | a0001c0005t0001g0005a0004c0007t0015g0162 | 2 | HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.100+15571G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119310575 | ||||||
| chr3:119310583
|
C | T | 104 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(101): Show | 105 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.100+15579C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119310583 | ||||||
| chr3:119310674
|
C | T | 1 | a0002c0003t0002g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.100+15670C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119310674 | ||||||
| chr3:119310723
|
G | A | 137 | a0001c0001t0005g0022a0001c0001t0005g0278a0001c0001t0006g0025others(134): Show | 138 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.100+15719G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119310723 | ||||||
| chr3:119310754
|
C | T | 4 | a0001c0005t0001g0160a0001c0005t0001g0163a0001c0005t0001g0164others(1): Show | 4 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+15750C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119310754 | ||||||
| chr3:119311044
|
T | G | 104 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(101): Show | 105 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.100+16040T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119311044 | ||||||
| chr3:119311105
|
C | T | 12 | a0001c0001t0011g0001a0001c0001t0011g0158a0001c0001t0011g0183others(9): Show | 13 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.100+16101C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119311105 | ||||||
| chr3:119311115
|
A | G | 1 | a0002c0003t0009g0201 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.100+16111A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119311115 | ||||||
| chr3:119311239
|
C | A | 7 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0005t0012g0285others(4): Show | 7 | HG00639.hp1 HG01106.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+16235C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119311239 | ||||||
| chr3:119311474
|
T | C | 104 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(101): Show | 105 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.100+16470T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119311474 | ||||||
| chr3:119311566
|
G | A | 137 | a0001c0001t0005g0022a0001c0001t0005g0278a0001c0001t0006g0025others(134): Show | 138 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.100+16562G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119311566 | ||||||
| chr3:119311638
|
T | C | 1 | a0003c0006t0056g0011 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.100+16634T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119311638 | ||||||
| chr3:119311732
|
G | A | 4 | a0001c0005t0001g0005a0001c0005t0001g0165a0001c0010t0014g0004others(1): Show | 4 | HG02280.hp2 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+16728G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119311732 | ||||||
| chr3:119311741
|
G | T | 1 | a0001c0001t0020g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.100+16737G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119311741 | ||||||
| chr3:119311832
|
T | C | 27 | a0001c0001t0011g0001a0001c0001t0011g0158a0001c0001t0011g0183others(24): Show | 28 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.100+16828T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119311832 | ||||||
| chr3:119311904
|
C | G | 1 | a0001c0001t0025g0204 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.100+16900C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119311904 | ||||||
| chr3:119312042
|
G | A | 104 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(101): Show | 105 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.100+17038G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119312042 | ||||||
| chr3:119312113
|
A | G | 114 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(111): Show | 115 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.100+17109A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119312113 | ||||||
| chr3:119312186
|
T | C | 1 | a0002c0003t0009g0248 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.100+17182T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119312186 | ||||||
| chr3:119312215
|
T | C | 113 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(110): Show | 114 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.100+17211T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119312215 | ||||||
| chr3:119312294
|
C | G | 198 | a0001c0001t0005g0022a0001c0001t0005g0077a0001c0001t0005g0078others(195): Show | 200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.100+17290C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119312294 | ||||||
| chr3:119312436
|
G | A | 7 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0005t0012g0285others(4): Show | 7 | HG00639.hp1 HG01106.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+17432G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119312436 | ||||||
| chr3:119312520
|
G | A | 9 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(6): Show | 9 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+17516G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119312520 | ||||||
| chr3:119312564
|
G | A | 40 | a0001c0001t0005g0278a0001c0001t0007g0234a0001c0001t0007g0275others(37): Show | 41 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.100+17560G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119312564 | ||||||
| chr3:119312566
|
C | T | 1 | a0002c0003t0002g0123 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.100+17562C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119312566 | ||||||
| chr3:119312567
|
T | G | 7 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0005t0012g0285others(4): Show | 7 | HG00639.hp1 HG01106.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+17563T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119312567 | ||||||
| chr3:119312652
|
A | G | 2 | a0001c0001t0020g0010a0003c0006t0001g0159 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.100+17648A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119312652 | ||||||
| chr3:119312684
|
C | T | 9 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(6): Show | 9 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+17680C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119312684 | ||||||
| chr3:119312798
|
C | T | 2 | a0001c0005t0001g0005a0004c0007t0015g0162 | 2 | HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.100+17794C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119312798 | ||||||
| chr3:119312884
|
A | T | 104 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(101): Show | 105 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.100+17880A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119312884 | ||||||
| chr3:119312885
|
G | T | 1 | a0001c0010t0014g0004 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100+17881G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119312885 | ||||||
| chr3:119313124
|
T | C | 1 | a0001c0004t0064g0061 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.100+18120T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119313124 | ||||||
| chr3:119313214
|
C | G | 4 | a0001c0005t0001g0160a0001c0005t0001g0163a0001c0005t0001g0164others(1): Show | 4 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+18210C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119313214 | ||||||
| chr3:119313291
|
T | C | 3 | a0001c0001t0017g0175a0001c0001t0017g0302a0001c0001t0017g0303 | 3 | NA18971.hp1 NA19081.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.100+18287T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119313291 | ||||||
| chr3:119313293
|
T | C | 1 | a0001c0001t0005g0278 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.100+18289T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119313293 | ||||||
| chr3:119313310
|
A | G | 1 | a0001c0005t0014g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.100+18306A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119313310 | ||||||
| chr3:119313413
|
A | G | 5 | a0001c0001t0020g0056a0001c0001t0060g0026a0001c0001t0061g0057others(2): Show | 5 | HG01884.hp2 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+18409A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119313413 | ||||||
| chr3:119313513
|
C | G | 117 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(114): Show | 118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.100+18509C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119313513 | ||||||
| chr3:119313579
|
C | G | 15 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0020g0043others(12): Show | 15 | HG01255.hp2 HG01975.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.100+18575C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119313579 | ||||||
| chr3:119313601
|
A | G | 21 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0020g0043others(18): Show | 21 | HG01255.hp2 HG01884.hp2 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.100+18597A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119313601 | ||||||
| chr3:119313610
|
C | CT | 4 | a0001c0001t0018g0207a0001c0001t0018g0208a0001c0001t0018g0209others(1): Show | 4 | HG02258.hp1 HG03654.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+18607dupT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119313610 | |||||
| chr3:119313700
|
T | C | 117 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(114): Show | 118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.100+18696T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119313700 | ||||||
| chr3:119313970
|
G | A | 2 | a0001c0001t0020g0010a0003c0006t0001g0159 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.100+18966G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119313970 | ||||||
| chr3:119314025
|
G | C | 4 | a0001c0005t0001g0005a0001c0005t0001g0165a0001c0010t0014g0004others(1): Show | 4 | HG02280.hp2 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+19021G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119314025 | ||||||
| chr3:119314085
|
C | T | 20 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0020g0043others(17): Show | 20 | HG01255.hp2 HG01884.hp2 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.100+19081C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119314085 | ||||||
| chr3:119314145
|
C | T | 12 | a0001c0001t0011g0001a0001c0001t0011g0158a0001c0001t0011g0183others(9): Show | 13 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.100+19141C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119314145 | ||||||
| chr3:119314283
|
G | C | 2 | a0001c0002t0001g0083a0001c0002t0001g0084 | 2 | NA18987.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.100+19279G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119314283 | ||||||
| chr3:119314310
|
A | G | 117 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(114): Show | 118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.100+19306A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119314310 | ||||||
| chr3:119314662
|
G | A | 1 | a0004c0007t0015g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.100+19658G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119314662 | ||||||
| chr3:119314739
|
C | A | 2 | a0001c0001t0007g0202a0001c0001t0007g0251 | 2 | NA18960.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.100+19735C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119314739 | ||||||
| chr3:119314767
|
C | T | 2 | a0001c0001t0020g0010a0003c0006t0001g0159 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.100+19763C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119314767 | ||||||
| chr3:119314776
|
G | A | 9 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(6): Show | 9 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+19772G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119314776 | ||||||
| chr3:119314897
|
G | A | 1 | a0001c0001t0025g0223 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.100+19893G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119314897 | ||||||
| chr3:119314900
|
T | C | 1 | a0001c0005t0014g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.100+19896T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119314900 | ||||||
| chr3:119314912
|
C | T | 13 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(10): Show | 13 | HG02083.hp1 HG02129.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.100+19908C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119314912 | ||||||
| chr3:119314942
|
C | A | 9 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(6): Show | 9 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+19938C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119314942 | ||||||
| chr3:119315075
|
G | A | 117 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(114): Show | 118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.100+20071G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119315075 | ||||||
| chr3:119315169
|
T | C | 1 | a0001c0002t0012g0206 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100+20165T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119315169 | ||||||
| chr3:119315172
|
T | C | 117 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(114): Show | 118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.100+20168T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119315172 | ||||||
| chr3:119315218
|
A | C | 7 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0005t0012g0285others(4): Show | 7 | HG00639.hp1 HG01106.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+20214A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119315218 | ||||||
| chr3:119315442
|
G | A | 1 | a0003c0006t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.100+20438G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119315442 | ||||||
| chr3:119315663
|
T | G | 118 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(115): Show | 119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.100+20659T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119315663 | ||||||
| chr3:119315736
|
G | A | 1 | a0001c0002t0037g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.100+20732G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119315736 | ||||||
| chr3:119315909
|
T | C | 228 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(225): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.100+20905T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119315909 | ||||||
| chr3:119315929
|
C | T | 1 | a0001c0001t0007g0241 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.100+20925C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119315929 | ||||||
| chr3:119316094
|
C | T | 1 | a0001c0010t0014g0004 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100+21090C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119316094 | ||||||
| chr3:119316361
|
A | C | 7 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0005t0012g0285others(4): Show | 7 | HG00639.hp1 HG01106.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+21357A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119316361 | ||||||
| chr3:119316383
|
T | C | 1 | a0001c0001t0006g0154 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.100+21379T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119316383 | ||||||
| chr3:119316387
|
T | A | 1 | a0002c0003t0002g0112 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.100+21383T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119316387 | ||||||
| chr3:119316526
|
C | G | 1 | a0002c0003t0009g0248 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.100+21522C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119316526 | ||||||
| chr3:119316569
|
G | A | 1 | a0002c0003t0002g0218 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.100+21565G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119316569 | ||||||
| chr3:119316757
|
G | A | 1 | a0013c0020t0013g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.100+21753G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119316757 | ||||||
| chr3:119316921
|
G | A | 2 | a0001c0001t0029g0054a0002c0003t0030g0053 | 2 | HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.100+21917G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119316921 | ||||||
| chr3:119316981
|
G | A | 1 | a0001c0005t0001g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.100+21977G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119316981 | ||||||
| chr3:119317028
|
A | G | 1 | a0001c0001t0005g0111 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.100+22024A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119317028 | ||||||
| chr3:119317032
|
G | A | 1 | a0001c0001t0029g0054 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.100+22028G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119317032 | ||||||
| chr3:119317060
|
A | T | 1 | a0001c0001t0008g0277 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.100+22056A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119317060 | ||||||
| chr3:119317178
|
T | A | 2 | a0004c0007t0044g0196a0004c0007t0054g0205 | 2 | HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.100+22174T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119317178 | ||||||
| chr3:119317183
|
CTT | C | 114 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(111): Show | 115 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.100+22191_100+2219 others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119317183 | |||||
| chr3:119317366
|
G | T | 9 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(6): Show | 9 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+22362G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119317366 | ||||||
| chr3:119317368
|
C | T | 1 | a0001c0001t0020g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.100+22364C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119317368 | ||||||
| chr3:119317369
|
G | A | 3 | a0001c0001t0006g0103a0001c0001t0006g0104a0001c0002t0001g0105 | 3 | NA18969.hp1 NA19003.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.100+22365G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119317369 | ||||||
| chr3:119317758
|
A | G | 1 | a0001c0010t0014g0004 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100+22754A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119317758 | ||||||
| chr3:119317805
|
G | A | 117 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(114): Show | 118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.100+22801G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119317805 | ||||||
| chr3:119317879
|
T | C | 9 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(6): Show | 9 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+22875T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119317879 | ||||||
| chr3:119317996
|
G | T | 117 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(114): Show | 118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.100+22992G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119317996 | ||||||
| chr3:119318002
|
G | A | 20 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0020g0043others(17): Show | 20 | HG01255.hp2 HG01884.hp2 HG01975.hp2 others(17): Show |
intron_variant | MODIFIER | c.100+22998G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119318002 | ||||||
| chr3:119318188
|
T | C | 3 | a0001c0002t0004g0247a0002c0003t0009g0220a0010c0016t0004g0166 | 3 | HG00735.hp2 HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.100+23184T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119318188 | ||||||
| chr3:119318292
|
G | A | 9 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(6): Show | 9 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+23288G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119318292 | ||||||
| chr3:119318352
|
G | A | 2 | a0001c0001t0029g0054a0002c0003t0030g0053 | 2 | HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.100+23348G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119318352 | ||||||
| chr3:119318425
|
C | T | 1 | a0001c0002t0012g0206 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100+23421C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119318425 | ||||||
| chr3:119318433
|
T | C | 1 | a0001c0002t0001g0101 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.100+23429T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119318433 | ||||||
| chr3:119318481
|
T | G | 6 | a0001c0001t0020g0056a0001c0001t0060g0026a0001c0001t0061g0057others(3): Show | 6 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+23477T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119318481 | ||||||
| chr3:119318679
|
T | C | 200 | a0001c0001t0005g0022a0001c0001t0005g0077a0001c0001t0005g0078others(197): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.100+23675T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119318679 | ||||||
| chr3:119318800
|
G | C | 21 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(18): Show | 21 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.100+23796G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119318800 | ||||||
| chr3:119318851
|
T | C | 1 | a0002c0003t0030g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.100+23847T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119318851 | ||||||
| chr3:119318993
|
C | T | 117 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(114): Show | 118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.100+23989C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119318993 | ||||||
| chr3:119319166
|
G | A | 2 | a0001c0005t0001g0005a0004c0007t0015g0162 | 2 | HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.100+24162G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119319166 | ||||||
| chr3:119319317
|
A | G | 2 | a0001c0001t0046g0307a0001c0001t0055g0306 | 2 | NA19060.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.100+24313A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119319317 | ||||||
| chr3:119319343
|
A | G | 3 | a0001c0004t0021g0048a0001c0004t0021g0059a0001c0005t0014g0047 | 3 | HG02055.hp1 HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.100+24339A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119319343 | ||||||
| chr3:119319360
|
G | A | 6 | a0001c0001t0007g0296a0001c0001t0008g0215a0001c0001t0008g0216others(3): Show | 6 | HG00738.hp1 HG00741.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+24356G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119319360 | ||||||
| chr3:119319463
|
G | C | 1 | a0001c0005t0014g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.100+24459G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119319463 | ||||||
| chr3:119319529
|
A | C | 1 | a0001c0001t0029g0054 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.100+24525A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119319529 | ||||||
| chr3:119319595
|
T | A | 4 | a0001c0005t0001g0005a0001c0005t0001g0165a0001c0010t0014g0004others(1): Show | 4 | HG02280.hp2 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+24591T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119319595 | ||||||
| chr3:119320043
|
A | G | 117 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(114): Show | 118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.100+25039A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119320043 | ||||||
| chr3:119320077
|
G | A | 2 | a0004c0007t0015g0016a0014c0014t0058g0003 | 2 | HG01884.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.100+25073G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119320077 | ||||||
| chr3:119320487
|
A | G | 1 | a0001c0001t0039g0260 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100+25483A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119320487 | ||||||
| chr3:119320530
|
C | A | 1 | a0001c0004t0003g0021 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.100+25526C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119320530 | ||||||
| chr3:119320876
|
T | C | 4 | a0001c0005t0001g0005a0001c0005t0001g0165a0001c0010t0014g0004others(1): Show | 4 | HG02280.hp2 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+25872T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119320876 | ||||||
| chr3:119320940
|
T | C | 7 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0005t0012g0285others(4): Show | 7 | HG00639.hp1 HG01106.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+25936T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119320940 | ||||||
| chr3:119321114
|
T | C | 21 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(18): Show | 21 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.100+26110T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119321114 | ||||||
| chr3:119321141
|
T | C | 7 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0005t0012g0285others(4): Show | 7 | HG00639.hp1 HG01106.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+26137T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119321141 | ||||||
| chr3:119321158
|
C | A | 1 | a0001c0001t0007g0250 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.100+26154C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119321158 | ||||||
| chr3:119321279
|
C | CTATATAT others(23): Show |
21 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(18): Show | 21 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.100+26303_100+2630 others(34): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119321279 | |||||
| chr3:119321279
|
CTA | C | 113 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(110): Show | 114 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.100+26290_100+2629 others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119321279 | |||||
| chr3:119321294
|
T | G | 3 | a0001c0005t0001g0005a0001c0010t0014g0004a0004c0007t0015g0162 | 3 | HG02280.hp2 HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.100+26290T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119321294 | ||||||
| chr3:119321295
|
A | T | 3 | a0001c0005t0001g0005a0001c0010t0014g0004a0004c0007t0015g0162 | 3 | HG02280.hp2 HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.100+26291A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119321295 | ||||||
| chr3:119321296
|
G | A | 4 | a0001c0005t0001g0005a0001c0005t0001g0165a0001c0010t0014g0004others(1): Show | 4 | HG02280.hp2 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+26292G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119321296 | ||||||
| chr3:119321335
|
T | C | 1 | a0001c0004t0021g0059 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.100+26331T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119321335 | ||||||
| chr3:119321471
|
G | A | 1 | a0002c0003t0031g0089 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.100+26467G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119321471 | ||||||
| chr3:119321512
|
G | A | 2 | a0002c0003t0009g0297a0002c0003t0009g0298 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.100+26508G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119321512 | ||||||
| chr3:119321546
|
G | A | 1 | a0001c0002t0012g0206 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100+26542G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119321546 | ||||||
| chr3:119321557
|
TTATATA | T | 4 | a0001c0001t0006g0103a0001c0001t0006g0104a0001c0002t0001g0105others(1): Show | 4 | NA18960.hp2 NA18969.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.100+26561_100+2656 others(10): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119321557 | |||||
| chr3:119321585
|
C | A | 2 | a0001c0001t0020g0064a0002c0003t0002g0063 | 2 | HG03239.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.100+26581C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119321585 | ||||||
| chr3:119321672
|
G | A | 2 | a0001c0001t0007g0241a0001c0002t0004g0291 | 2 | HG02602.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.100+26668G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119321672 | ||||||
| chr3:119321676
|
A | G | 117 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(114): Show | 118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.100+26672A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119321676 | ||||||
| chr3:119321678
|
T | A | 4 | a0001c0005t0001g0160a0001c0005t0001g0163a0001c0005t0001g0164others(1): Show | 4 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+26674T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119321678 | ||||||
| chr3:119321730
|
C | G | 1 | a0001c0005t0001g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.100+26726C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119321730 | ||||||
| chr3:119321794
|
C | G | 9 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(6): Show | 9 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+26790C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119321794 | ||||||
| chr3:119321877
|
T | G | 1 | a0001c0004t0003g0136 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.100+26873T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119321877 | ||||||
| chr3:119321887
|
G | T | 1 | a0001c0002t0034g0240 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.100+26883G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119321887 | ||||||
| chr3:119322312
|
C | T | 9 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(6): Show | 9 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+27308C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119322312 | ||||||
| chr3:119322370
|
G | C | 1 | a0001c0002t0004g0230 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.100+27366G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119322370 | ||||||
| chr3:119322386
|
T | A | 21 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0020g0043others(18): Show | 21 | HG01255.hp2 HG01884.hp2 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.100+27382T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119322386 | ||||||
| chr3:119322454
|
T | C | 4 | a0001c0005t0001g0005a0001c0005t0001g0165a0001c0010t0014g0004others(1): Show | 4 | HG02280.hp2 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+27450T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119322454 | ||||||
| chr3:119322454
|
T | G | 2 | a0002c0003t0009g0297a0002c0003t0009g0298 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.100+27450T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119322454 | ||||||
| chr3:119322460
|
G | A | 16 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0020g0043others(13): Show | 16 | HG01255.hp2 HG01975.hp2 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.100+27456G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119322460 | ||||||
| chr3:119322561
|
C | G | 113 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(110): Show | 114 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.100+27557C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119322561 | ||||||
| chr3:119322562
|
C | T | 4 | a0001c0005t0001g0005a0001c0005t0001g0165a0001c0010t0014g0004others(1): Show | 4 | HG02280.hp2 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+27558C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119322562 | ||||||
| chr3:119322600
|
C | T | 2 | a0001c0005t0001g0005a0004c0007t0015g0162 | 2 | HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.100+27596C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119322600 | ||||||
| chr3:119322656
|
A | G | 2 | a0004c0007t0044g0196a0004c0007t0054g0205 | 2 | HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.100+27652A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119322656 | ||||||
| chr3:119322767
|
T | C | 3 | a0001c0005t0001g0005a0001c0005t0001g0165a0004c0007t0015g0162 | 3 | HG02559.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.100+27763T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119322767 | ||||||
| chr3:119322817
|
C | CT | 5 | a0001c0001t0052g0283a0001c0005t0012g0285a0001c0005t0012g0287others(2): Show | 5 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+27814dupT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119322817 | |||||
| chr3:119322836
|
G | C | 1 | a0001c0010t0014g0004 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100+27832G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119322836 | ||||||
| chr3:119322843
|
G | C | 9 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(6): Show | 9 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+27839G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119322843 | ||||||
| chr3:119322877
|
C | CG | 9 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(6): Show | 9 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+27878dupG | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119322877 | |||||
| chr3:119322963
|
T | A | 2 | a0004c0007t0044g0196a0004c0007t0054g0205 | 2 | HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.100+27959T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119322963 | ||||||
| chr3:119322978
|
T | C | 117 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(114): Show | 118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.100+27974T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119322978 | ||||||
| chr3:119323125
|
G | A | 1 | a0001c0004t0010g0195 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.100+28121G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119323125 | ||||||
| chr3:119323459
|
T | G | 104 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(101): Show | 105 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.100+28455T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119323459 | ||||||
| chr3:119323465
|
G | T | 15 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0020g0043others(12): Show | 15 | HG01255.hp2 HG01975.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.100+28461G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119323465 | ||||||
| chr3:119323708
|
G | A | 4 | a0001c0005t0001g0005a0001c0005t0001g0165a0001c0010t0014g0004others(1): Show | 4 | HG02280.hp2 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+28704G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119323708 | ||||||
| chr3:119323741
|
C | T | 2 | a0001c0002t0004g0247a0002c0003t0009g0220 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.100+28737C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119323741 | ||||||
| chr3:119323920
|
C | T | 9 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(6): Show | 9 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+28916C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119323920 | ||||||
| chr3:119323921
|
C | G | 21 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0020g0043others(18): Show | 21 | HG01255.hp2 HG01884.hp2 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.100+28917C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119323921 | ||||||
| chr3:119324093
|
G | A | 2 | a0004c0007t0044g0196a0004c0007t0054g0205 | 2 | HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.100+29089G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119324093 | ||||||
| chr3:119324116
|
T | C | 15 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0020g0043others(12): Show | 15 | HG01255.hp2 HG01975.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.100+29112T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119324116 | ||||||
| chr3:119324164
|
C | G | 104 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(101): Show | 105 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.100+29160C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119324164 | ||||||
| chr3:119324352
|
C | A | 2 | a0001c0001t0029g0054a0002c0003t0030g0053 | 2 | HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.100+29348C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119324352 | ||||||
| chr3:119324711
|
A | G | 3 | a0001c0005t0001g0005a0001c0005t0001g0165a0004c0007t0015g0162 | 3 | HG02559.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.100+29707A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119324711 | ||||||
| chr3:119324902
|
G | A | 21 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0020g0043others(18): Show | 21 | HG01255.hp2 HG01884.hp2 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.100+29898G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119324902 | ||||||
| chr3:119324985
|
T | A | 1 | a0003c0006t0013g0006 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.100+29981T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119324985 | ||||||
| chr3:119325010
|
T | C | 1 | a0001c0001t0008g0252 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.100+30006T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119325010 | ||||||
| chr3:119325140
|
T | C | 1 | a0001c0001t0020g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.100+30136T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119325140 | ||||||
| chr3:119325154
|
T | C | 1 | a0001c0001t0008g0180 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.100+30150T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119325154 | ||||||
| chr3:119325375
|
G | A | 1 | a0001c0005t0001g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100+30371G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119325375 | ||||||
| chr3:119325430
|
C | T | 1 | a0004c0007t0015g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.100+30426C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119325430 | ||||||
| chr3:119325482
|
C | T | 6 | a0001c0001t0052g0283a0001c0005t0012g0285a0001c0005t0012g0287others(3): Show | 6 | HG00639.hp1 HG01106.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+30478C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119325482 | ||||||
| chr3:119325515
|
C | T | 4 | a0001c0005t0001g0005a0001c0005t0001g0165a0001c0010t0014g0004others(1): Show | 4 | HG02280.hp2 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+30511C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119325515 | ||||||
| chr3:119325522
|
T | C | 119 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(116): Show | 120 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.100+30518T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119325522 | ||||||
| chr3:119325647
|
A | G | 172 | a0001c0001t0005g0022a0001c0001t0005g0077a0001c0001t0005g0078others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.100+30643A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119325647 | ||||||
| chr3:119325655
|
G | A | 2 | a0001c0001t0029g0054a0002c0003t0030g0053 | 2 | HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.100+30651G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119325655 | ||||||
| chr3:119325660
|
G | C | 4 | a0001c0002t0004g0235a0001c0004t0010g0176a0001c0004t0010g0222others(1): Show | 4 | HG00099.hp2 HG01167.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+30656G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119325660 | ||||||
| chr3:119325672
|
G | A | 2 | a0004c0007t0044g0196a0004c0007t0054g0205 | 2 | HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.100+30668G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119325672 | ||||||
| chr3:119325695
|
A | T | 5 | a0001c0001t0052g0283a0001c0005t0012g0285a0001c0005t0012g0287others(2): Show | 5 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+30691A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119325695 | ||||||
| chr3:119325731
|
G | A | 9 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(6): Show | 9 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+30727G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119325731 | ||||||
| chr3:119325809
|
T | A | 7 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0005t0012g0285others(4): Show | 7 | HG00639.hp1 HG01106.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+30805T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119325809 | ||||||
| chr3:119325848
|
C | T | 1 | a0001c0010t0014g0004 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.100+30844C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119325848 | ||||||
| chr3:119325909
|
G | A | 4 | a0001c0005t0001g0005a0001c0005t0001g0165a0001c0010t0014g0004others(1): Show | 4 | HG02280.hp2 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+30905G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119325909 | ||||||
| chr3:119326053
|
G | A | 1 | a0002c0003t0062g0093 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.100+31049G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326053 | ||||||
| chr3:119326063
|
G | A | 4 | a0001c0005t0001g0005a0001c0005t0001g0165a0001c0010t0014g0004others(1): Show | 4 | HG02280.hp2 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+31059G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326063 | ||||||
| chr3:119326065
|
G | A | 5 | a0001c0001t0006g0124a0001c0001t0008g0170a0001c0002t0001g0134others(2): Show | 5 | NA18956.hp2 NA18999.hp1 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+31061G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326065 | ||||||
| chr3:119326158
|
C | A | 1 | a0001c0004t0003g0147 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.100+31154C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326158 | ||||||
| chr3:119326203
|
G | A | 4 | a0001c0005t0001g0005a0001c0005t0001g0165a0001c0010t0014g0004others(1): Show | 4 | HG02280.hp2 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+31199G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326203 | ||||||
| chr3:119326276
|
G | A | 100 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(97): Show | 101 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.100+31272G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326276 | ||||||
| chr3:119326351
|
G | A | 3 | a0001c0005t0001g0163a0001c0005t0001g0164a0003c0006t0001g0161 | 3 | HG02572.hp1 HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.100+31347G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326351 | ||||||
| chr3:119326365
|
A | T | 1 | a0002c0003t0009g0194 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.100+31361A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326365 | ||||||
| chr3:119326457
|
G | A | 104 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(101): Show | 105 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.100+31453G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326457 | ||||||
| chr3:119326466
|
C | T | 1 | a0001c0004t0003g0076 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.100+31462C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326466 | ||||||
| chr3:119326535
|
C | T | 3 | a0001c0005t0001g0163a0001c0005t0001g0164a0003c0006t0001g0161 | 3 | HG02572.hp1 HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.100+31531C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326535 | ||||||
| chr3:119326569
|
C | T | 1 | a0001c0005t0001g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.100+31565C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326569 | ||||||
| chr3:119326650
|
G | T | 9 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(6): Show | 9 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.100+31646G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326650 | ||||||
| chr3:119326756
|
G | A | 1 | a0001c0002t0012g0206 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100+31752G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326756 | ||||||
| chr3:119326770
|
G | A | 117 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(114): Show | 118 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.100+31766G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326770 | ||||||
| chr3:119326771
|
T | C | 4 | a0001c0005t0001g0005a0001c0005t0001g0165a0001c0010t0014g0004others(1): Show | 4 | HG02280.hp2 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+31767T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326771 | ||||||
| chr3:119326861
|
G | C | 1 | a0001c0001t0011g0184 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.100+31857G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326861 | ||||||
| chr3:119326895
|
T | C | 1 | a0004c0007t0015g0016 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.100+31891T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326895 | ||||||
| chr3:119326956
|
G | A | 1 | a0001c0002t0001g0070 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.100+31952G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119326956 | ||||||
| chr3:119327171
|
A | G | 4 | a0001c0005t0001g0005a0001c0005t0001g0165a0001c0010t0014g0004others(1): Show | 4 | HG02280.hp2 HG02559.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+32167A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119327171 | ||||||
| chr3:119327185
|
T | A | 1 | a0001c0002t0004g0236 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.100+32181T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119327185 | ||||||
| chr3:119327208
|
T | C | 2 | a0001c0001t0029g0054a0002c0003t0030g0053 | 2 | HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.100+32204T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119327208 | ||||||
| chr3:119327264
|
C | T | 5 | a0001c0001t0020g0056a0001c0001t0060g0026a0001c0001t0061g0057others(2): Show | 5 | HG01884.hp2 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+32260C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119327264 | ||||||
| chr3:119327284
|
T | C | 1 | a0002c0003t0041g0295 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.100+32280T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119327284 | ||||||
| chr3:119327386
|
A | G | 1 | a0005c0008t0002g0122 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.100+32382A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119327386 | ||||||
| chr3:119327469
|
C | T | 1 | a0001c0001t0017g0189 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.100+32465C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119327469 | ||||||
| chr3:119327686
|
T | A | 99 | a0001c0001t0005g0278a0001c0001t0007g0202a0001c0001t0007g0225others(96): Show | 100 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.100+32682T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119327686 | ||||||
| chr3:119327797
|
A | T | 4 | a0001c0001t0011g0001a0001c0001t0011g0184a0001c0001t0011g0188others(1): Show | 5 | HG01081.hp2 HG01358.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+32793A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119327797 | ||||||
| chr3:119328021
|
C | A | 2 | a0001c0001t0020g0010a0003c0006t0001g0159 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.100+33017C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119328021 | ||||||
| chr3:119328080
|
T | C | 1 | a0001c0001t0018g0209 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.100+33076T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119328080 | ||||||
| chr3:119328241
|
A | C | 1 | a0002c0003t0002g0218 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.100+33237A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119328241 | ||||||
| chr3:119328260
|
G | A | 2 | a0003c0006t0022g0269a0003c0006t0022g0270 | 2 | HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.100+33256G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119328260 | ||||||
| chr3:119328441
|
T | C | 1 | a0003c0006t0022g0269 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.100+33437T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119328441 | ||||||
| chr3:119328513
|
G | A | 27 | a0001c0001t0005g0022a0001c0001t0006g0025a0001c0001t0020g0043others(24): Show | 27 | HG00639.hp1 HG01106.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.100+33509G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119328513 | ||||||
| chr3:119328633
|
T | C | 121 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(118): Show | 122 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.100+33629T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119328633 | ||||||
| chr3:119328709
|
T | C | 2 | a0001c0001t0029g0054a0002c0003t0030g0053 | 2 | HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.100+33705T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119328709 | ||||||
| chr3:119328744
|
G | A | 4 | a0001c0005t0001g0160a0001c0005t0001g0163a0001c0005t0001g0164others(1): Show | 4 | HG02572.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+33740G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119328744 | ||||||
| chr3:119328778
|
C | A | 11 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(8): Show | 11 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.100+33774C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119328778 | ||||||
| chr3:119328787
|
C | T | 1 | a0002c0003t0009g0263 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.100+33783C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119328787 | ||||||
| chr3:119328825
|
A | T | 1 | a0002c0003t0041g0295 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.100+33821A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119328825 | ||||||
| chr3:119328856
|
G | A | 6 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0046g0307others(3): Show | 6 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+33852G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119328856 | ||||||
| chr3:119328919
|
T | C | 1 | a0013c0020t0013g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.100+33915T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119328919 | ||||||
| chr3:119328973
|
T | G | 1 | a0001c0002t0012g0206 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100+33969T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119328973 | ||||||
| chr3:119329046
|
T | C | 7 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0046g0307others(4): Show | 7 | HG02083.hp1 HG02129.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+34042T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119329046 | ||||||
| chr3:119329245
|
T | C | 126 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(123): Show | 127 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.100+34241T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119329245 | ||||||
| chr3:119329260
|
G | A | 3 | a0001c0001t0006g0102a0001c0004t0003g0113a0001c0004t0003g0125 | 3 | HG00741.hp2 HG01243.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.100+34256G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119329260 | ||||||
| chr3:119329282
|
A | G | 126 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(123): Show | 127 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.100+34278A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119329282 | ||||||
| chr3:119329348
|
G | A | 2 | a0001c0004t0003g0150a0002c0003t0002g0152 | 2 | HG03669.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.100+34344G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119329348 | ||||||
| chr3:119329373
|
C | T | 1 | a0001c0001t0007g0228 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.100+34369C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119329373 | ||||||
| chr3:119329472
|
A | C | 10 | a0001c0001t0020g0043a0001c0001t0029g0042a0001c0001t0050g0177others(7): Show | 10 | HG02015.hp2 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.100+34468A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119329472 | ||||||
| chr3:119329667
|
G | A | 1 | a0012c0015t0035g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.100+34663G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119329667 | ||||||
| chr3:119329668
|
C | A | 1 | a0012c0015t0035g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.100+34664C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119329668 | ||||||
| chr3:119329835
|
G | A | 2 | a0003c0006t0013g0041a0003c0006t0013g0045 | 2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.100+34831G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119329835 | ||||||
| chr3:119329869
|
T | C | 6 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0046g0307others(3): Show | 6 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+34865T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119329869 | ||||||
| chr3:119330025
|
T | A | 5 | a0001c0002t0001g0008a0001c0004t0003g0007a0001c0005t0014g0009others(2): Show | 5 | HG01496.hp1 HG02818.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+35021T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119330025 | ||||||
| chr3:119330071
|
C | A | 5 | a0001c0005t0001g0160a0001c0005t0001g0163a0001c0005t0001g0164others(2): Show | 5 | HG01106.hp2 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+35067C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119330071 | ||||||
| chr3:119330107
|
G | A | 1 | a0001c0002t0034g0240 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.100+35103G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119330107 | ||||||
| chr3:119330224
|
T | G | 35 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(32): Show | 35 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.101-35092T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119330224 | ||||||
| chr3:119330382
|
A | T | 122 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(119): Show | 123 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.101-34934A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119330382 | ||||||
| chr3:119330704
|
A | G | 10 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(7): Show | 10 | HG02602.hp1 HG02738.hp2 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-34612A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119330704 | ||||||
| chr3:119330718
|
T | C | 1 | a0001c0004t0003g0110 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.101-34598T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119330718 | ||||||
| chr3:119330748
|
T | A | 1 | a0002c0003t0002g0112 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.101-34568T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119330748 | ||||||
| chr3:119330880
|
A | T | 2 | a0001c0001t0020g0010a0003c0006t0001g0159 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.101-34436A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119330880 | ||||||
| chr3:119330900
|
A | G | 2 | a0003c0006t0022g0269a0003c0006t0022g0270 | 2 | HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.101-34416A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119330900 | ||||||
| chr3:119331052
|
C | A | 5 | a0001c0001t0020g0056a0001c0001t0060g0026a0001c0001t0061g0057others(2): Show | 5 | HG01884.hp2 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-34264C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119331052 | ||||||
| chr3:119331158
|
G | T | 6 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0046g0307others(3): Show | 6 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-34158G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119331158 | ||||||
| chr3:119331506
|
A | G | 1 | a0002c0003t0002g0218 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.101-33810A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119331506 | ||||||
| chr3:119331550
|
C | T | 2 | a0004c0007t0044g0196a0004c0007t0054g0205 | 2 | HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.101-33766C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119331550 | ||||||
| chr3:119331638
|
C | G | 1 | a0001c0004t0003g0076 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.101-33678C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119331638 | ||||||
| chr3:119331828
|
A | G | 1 | a0003c0006t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.101-33488A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119331828 | ||||||
| chr3:119331885
|
G | T | 122 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(119): Show | 123 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.101-33431G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119331885 | ||||||
| chr3:119331902
|
C | T | 35 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(32): Show | 35 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.101-33414C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119331902 | ||||||
| chr3:119332019
|
C | A | 1 | a0001c0005t0014g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.101-33297C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119332019 | ||||||
| chr3:119332216
|
T | C | 2 | a0001c0001t0006g0065a0001c0001t0006g0066 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.101-33100T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119332216 | ||||||
| chr3:119332418
|
T | C | 2 | a0001c0005t0001g0165a0001c0010t0014g0004 | 2 | HG02280.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.101-32898T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119332418 | ||||||
| chr3:119332602
|
C | G | 1 | a0001c0001t0060g0026 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.101-32714C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119332602 | ||||||
| chr3:119332604
|
T | C | 5 | a0001c0001t0005g0278a0001c0001t0008g0277a0001c0002t0016g0279others(2): Show | 6 | HG02080.hp1 HG02155.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-32712T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119332604 | ||||||
| chr3:119332604
|
T | TTC | 4 | a0001c0001t0006g0092a0001c0002t0016g0133a0001c0004t0010g0219others(1): Show | 4 | HG00438.hp2 HG02523.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-32681_101-3268 others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332604 | |||||
| chr3:119332604
|
T | TTCTCTC | 3 | a0001c0004t0003g0039a0001c0004t0003g0040a0001c0005t0014g0028 | 3 | HG02451.hp2 HG02886.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.101-32685_101-3268 others(10): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332604 | |||||
| chr3:119332604
|
T | TTCTCTCT others(3): Show |
1 | a0001c0005t0027g0044 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.101-32689_101-3268 others(14): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332604 | |||||
| chr3:119332604
|
TTC | T | 3 | a0001c0002t0012g0238a0002c0003t0009g0265a0002c0003t0031g0089 | 3 | HG00597.hp1 HG01496.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.101-32681_101-3268 others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332604 | |||||
| chr3:119332625
|
TCTCTCTC others(7): Show |
T | 1 | a0001c0002t0012g0206 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.101-32689_101-3267 others(18): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332625 | |||||
| chr3:119332627
|
TCTCTCTC others(13): Show |
T | 4 | a0001c0001t0005g0058a0001c0004t0064g0061a0001c0005t0001g0005others(1): Show | 4 | HG02559.hp2 NA19070.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-32687_101-3266 others(24): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332627 | |||||
| chr3:119332629
|
TCTCTCTC others(5): Show |
T | 10 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0020g0056others(7): Show | 10 | HG01884.hp2 HG02083.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.101-32685_101-3267 others(16): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332629 | |||||
| chr3:119332629
|
TCTCTCTC others(9): Show |
T | 1 | a0001c0010t0014g0004 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.101-32685_101-3267 others(20): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332629 | |||||
| chr3:119332629
|
TCTCTCTC others(11): Show |
T | 1 | a0001c0005t0001g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.101-32685_101-3266 others(22): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332629 | |||||
| chr3:119332631
|
TCTCTCA | T | 16 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(13): Show | 16 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.101-32683_101-3267 others(10): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332631 | |||||
| chr3:119332631
|
TCTCTCAC others(3): Show |
T | 3 | a0001c0001t0018g0209a0001c0002t0001g0070a0002c0003t0019g0182 | 3 | HG01361.hp1 HG02970.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.101-32683_101-3267 others(14): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332631 | |||||
| chr3:119332631
|
TCTCTCAC others(5): Show |
T | 1 | a0001c0002t0018g0305 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.101-32683_101-3267 others(16): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332631 | |||||
| chr3:119332631
|
TCTCTCAC others(9): Show |
T | 27 | a0001c0001t0008g0224a0001c0001t0020g0064a0001c0001t0029g0054others(24): Show | 27 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.101-32683_101-3266 others(20): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332631 | |||||
| chr3:119332631
|
TCTCTCAC others(11): Show |
T | 5 | a0001c0001t0007g0241a0001c0001t0020g0010a0001c0002t0004g0291others(2): Show | 5 | HG02451.hp1 HG02602.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-32683_101-3266 others(22): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332631 | |||||
| chr3:119332633
|
T | A | 1 | a0001c0002t0001g0083 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.101-32683T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119332633 | ||||||
| chr3:119332633
|
T | TCA | 5 | a0001c0001t0008g0277a0001c0005t0004g0253a0002c0003t0002g0137others(2): Show | 5 | HG02155.hp2 HG03540.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-32682_101-3268 others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332633 | |||||
| chr3:119332633
|
TCTCA | T | 3 | a0001c0001t0007g0293a0002c0003t0002g0081a0002c0003t0031g0138 | 3 | HG00639.hp2 HG01978.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.101-32681_101-3267 others(8): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332633 | |||||
| chr3:119332633
|
TCTCACAC others(1): Show |
T | 3 | a0001c0001t0007g0254a0001c0002t0004g0255a0002c0003t0009g0264 | 3 | HG00609.hp2 NA18987.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.101-32681_101-3267 others(12): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332633 | |||||
| chr3:119332633
|
TCTCACAC others(3): Show |
T | 15 | a0001c0001t0011g0001a0001c0001t0011g0158a0001c0001t0011g0183others(12): Show | 16 | HG01081.hp2 HG01099.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.101-32681_101-3267 others(14): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332633 | |||||
| chr3:119332633
|
TCTCACAC others(5): Show |
T | 1 | a0001c0005t0001g0046 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.101-32681_101-3267 others(16): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332633 | |||||
| chr3:119332633
|
TCTCACAC others(7): Show |
T | 10 | a0001c0005t0001g0029a0001c0005t0001g0034a0001c0005t0001g0035others(7): Show | 10 | HG01106.hp2 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.101-32681_101-3266 others(18): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332633 | |||||
| chr3:119332633
|
TCTCACAC others(9): Show |
T | 3 | a0001c0001t0006g0065a0001c0001t0006g0066a0013c0020t0013g0051 | 3 | HG03491.hp2 HG03492.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.101-32681_101-3266 others(20): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332633 | |||||
| chr3:119332635
|
T | A | 17 | a0001c0001t0008g0277a0001c0001t0024g0243a0001c0001t0039g0260others(14): Show | 18 | HG00408.hp1 HG00597.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-32681T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119332635 | ||||||
| chr3:119332635
|
T | TCA | 69 | a0001c0001t0005g0022a0001c0001t0005g0117a0001c0001t0005g0129others(66): Show | 69 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.101-32641_101-3264 others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332635 | |||||
| chr3:119332635
|
T | TCACA | 27 | a0001c0001t0005g0096a0001c0001t0005g0111a0001c0001t0006g0027others(24): Show | 27 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.101-32643_101-3264 others(8): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332635 | |||||
| chr3:119332635
|
T | TCACACA | 10 | a0001c0001t0006g0148a0001c0001t0008g0192a0001c0001t0008g0215others(7): Show | 10 | HG00323.hp1 HG01261.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-32645_101-3264 others(10): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332635 | |||||
| chr3:119332635
|
T | TCTCA | 3 | a0001c0001t0006g0102a0001c0004t0010g0176a0001c0005t0001g0190 | 3 | HG01243.hp1 HG03669.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.101-32680_101-3267 others(8): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332635 | |||||
| chr3:119332635
|
T | TCTCACA | 4 | a0001c0002t0004g0235a0001c0004t0066g0217a0002c0003t0009g0297others(1): Show | 4 | HG01261.hp2 HG03490.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-32680_101-3267 others(10): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332635 | |||||
| chr3:119332635
|
TCA | T | 8 | a0001c0001t0007g0275a0001c0001t0024g0221a0001c0002t0004g0247others(5): Show | 8 | HG00735.hp2 HG02145.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.101-32641_101-3264 others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332635 | |||||
| chr3:119332635
|
TCACA | T | 12 | a0001c0001t0007g0202a0001c0001t0007g0249a0001c0001t0007g0250others(9): Show | 12 | HG00408.hp2 HG03490.hp2 NA18940.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-32643_101-3264 others(8): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332635 | |||||
| chr3:119332635
|
TCACACAC others(3): Show |
T | 7 | a0001c0001t0011g0186a0001c0001t0045g0286a0001c0001t0052g0283others(4): Show | 7 | HG00639.hp1 HG00735.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-32649_101-3264 others(14): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119332635 | |||||
| chr3:119332637
|
A | T | 12 | a0001c0001t0006g0092a0001c0001t0008g0273a0001c0001t0020g0043others(9): Show | 12 | HG00438.hp2 HG02015.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.101-32679A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119332637 | ||||||
| chr3:119332639
|
A | T | 13 | a0001c0001t0006g0092a0001c0001t0008g0273a0001c0001t0020g0043others(10): Show | 13 | HG00438.hp2 HG02015.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.101-32677A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119332639 | ||||||
| chr3:119332641
|
A | T | 23 | a0001c0001t0006g0092a0001c0001t0007g0202a0001c0001t0007g0249others(20): Show | 23 | HG00408.hp2 HG00438.hp2 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.101-32675A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119332641 | ||||||
| chr3:119332643
|
A | T | 8 | a0001c0001t0008g0212a0001c0001t0020g0043a0001c0001t0050g0177others(5): Show | 8 | HG02015.hp2 HG02056.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.101-32673A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119332643 | ||||||
| chr3:119332645
|
A | T | 1 | a0001c0001t0008g0200 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.101-32671A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119332645 | ||||||
| chr3:119332676
|
C | T | 1 | a0001c0002t0012g0206 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.101-32640C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119332676 | ||||||
| chr3:119332685
|
G | A | 6 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0046g0307others(3): Show | 6 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-32631G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119332685 | ||||||
| chr3:119332721
|
A | G | 35 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(32): Show | 35 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.101-32595A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119332721 | ||||||
| chr3:119332795
|
A | G | 7 | a0001c0001t0020g0010a0001c0005t0001g0160a0001c0005t0001g0163others(4): Show | 7 | HG01106.hp2 HG02451.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-32521A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119332795 | ||||||
| chr3:119332996
|
C | T | 23 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(20): Show | 23 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.101-32320C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119332996 | ||||||
| chr3:119333095
|
G | A | 6 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0046g0307others(3): Show | 6 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-32221G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119333095 | ||||||
| chr3:119333136
|
G | T | 6 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0005t0012g0285others(3): Show | 6 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.101-32180G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119333136 | ||||||
| chr3:119333142
|
A | G | 23 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(20): Show | 23 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.101-32174A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119333142 | ||||||
| chr3:119333150
|
A | C | 10 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(7): Show | 10 | HG02602.hp1 HG02738.hp2 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-32166A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119333150 | ||||||
| chr3:119333185
|
C | T | 1 | a0001c0005t0014g0062 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.101-32131C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119333185 | ||||||
| chr3:119333229
|
G | C | 6 | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0046g0307others(3): Show | 6 | HG02083.hp1 HG02129.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-32087G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119333229 | ||||||
| chr3:119333240
|
T | C | 1 | a0001c0001t0042g0282 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.101-32076T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119333240 | ||||||
| chr3:119333530
|
A | G | 1 | a0001c0004t0003g0024 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.101-31786A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119333530 | ||||||
| chr3:119333641
|
C | G | 90 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(87): Show | 90 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.101-31675C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119333641 | ||||||
| chr3:119333744
|
G | A | 90 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(87): Show | 90 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.101-31572G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119333744 | ||||||
| chr3:119333762
|
C | T | 7 | a0001c0001t0006g0092a0001c0001t0007g0202a0001c0001t0007g0251others(4): Show | 7 | HG00438.hp2 HG01884.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-31554C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119333762 | ||||||
| chr3:119333796
|
G | A | 1 | a0002c0003t0002g0152 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.101-31520G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119333796 | ||||||
| chr3:119333956
|
A | G | 17 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(14): Show | 17 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-31360A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119333956 | ||||||
| chr3:119333957
|
T | C | 4 | a0001c0005t0001g0034a0001c0005t0001g0046a0004c0007t0044g0196others(1): Show | 4 | HG02257.hp1 HG02280.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-31359T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119333957 | ||||||
| chr3:119334217
|
C | A | 1 | a0001c0001t0011g0301 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.101-31099C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119334217 | ||||||
| chr3:119334404
|
A | C | 1 | a0001c0001t0024g0221 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.101-30912A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119334404 | ||||||
| chr3:119334521
|
T | C | 8 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0001t0060g0026others(5): Show | 8 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.101-30795T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119334521 | ||||||
| chr3:119334615
|
T | G | 53 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(50): Show | 53 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(50): Show |
intron_variant | MODIFIER | c.101-30701T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119334615 | ||||||
| chr3:119334647
|
G | C | 2 | a0001c0002t0028g0017a0001c0002t0028g0018 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.101-30669G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119334647 | ||||||
| chr3:119334663
|
T | G | 2 | a0001c0001t0020g0064a0002c0003t0002g0063 | 2 | HG03239.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.101-30653T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119334663 | ||||||
| chr3:119334747
|
A | G | 1 | a0001c0005t0001g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.101-30569A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119334747 | ||||||
| chr3:119334794
|
T | C | 1 | a0001c0001t0008g0200 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.101-30522T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119334794 | ||||||
| chr3:119334807
|
T | C | 1 | a0002c0003t0002g0060 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.101-30509T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119334807 | ||||||
| chr3:119334841
|
C | T | 11 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(8): Show | 11 | HG00609.hp1 HG02083.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.101-30475C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119334841 | ||||||
| chr3:119334962
|
T | C | 11 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(8): Show | 11 | HG00609.hp1 HG02083.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.101-30354T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119334962 | ||||||
| chr3:119335079
|
T | TG | 27 | a0001c0001t0006g0127a0001c0001t0011g0001a0001c0001t0011g0158others(24): Show | 28 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.101-30234dupG | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119335079 | |||||
| chr3:119335082
|
G | GA | 45 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(42): Show | 45 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.101-30224dupA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119335082 | |||||
| chr3:119335156
|
C | T | 2 | a0001c0001t0006g0127a0001c0002t0001g0088 | 2 | HG01192.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.101-30160C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119335156 | ||||||
| chr3:119335360
|
A | T | 13 | a0001c0001t0039g0260a0001c0002t0001g0014a0001c0002t0028g0017others(10): Show | 13 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.101-29956A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119335360 | ||||||
| chr3:119335427
|
T | G | 1 | a0004c0007t0054g0205 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.101-29889T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119335427 | ||||||
| chr3:119335503
|
G | A | 2 | a0001c0001t0029g0054a0002c0003t0030g0053 | 2 | HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.101-29813G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119335503 | ||||||
| chr3:119335579
|
A | C | 1 | a0001c0001t0007g0249 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.101-29737A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119335579 | ||||||
| chr3:119335729
|
C | T | 22 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(19): Show | 22 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-29587C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119335729 | ||||||
| chr3:119335804
|
G | T | 4 | a0001c0001t0006g0103a0001c0001t0006g0104a0001c0002t0001g0105others(1): Show | 4 | NA18960.hp2 NA18969.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-29512G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119335804 | ||||||
| chr3:119335813
|
C | T | 1 | a0002c0003t0062g0093 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.101-29503C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119335813 | ||||||
| chr3:119335858
|
C | A | 1 | a0001c0001t0008g0200 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.101-29458C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119335858 | ||||||
| chr3:119335864
|
T | C | 155 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(152): Show | 156 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.101-29452T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119335864 | ||||||
| chr3:119335966
|
A | C | 1 | a0001c0002t0016g0279 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.101-29350A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119335966 | ||||||
| chr3:119336089
|
C | A | 4 | a0001c0004t0021g0048a0001c0004t0021g0059a0001c0005t0014g0047others(1): Show | 4 | HG02055.hp1 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-29227C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119336089 | ||||||
| chr3:119336131
|
C | T | 3 | a0001c0001t0040g0257a0001c0005t0001g0160a0001c0005t0004g0258 | 3 | HG02622.hp2 HG02818.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.101-29185C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119336131 | ||||||
| chr3:119336475
|
A | C | 30 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(27): Show | 30 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.101-28841A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119336475 | ||||||
| chr3:119336482
|
G | A | 1 | a0001c0005t0014g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.101-28834G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119336482 | ||||||
| chr3:119336536
|
A | C | 1 | a0001c0005t0001g0049 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.101-28780A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119336536 | ||||||
| chr3:119336632
|
GTTTTAT | G | 3 | a0001c0004t0003g0038a0001c0004t0003g0039a0001c0004t0003g0040 | 3 | HG02451.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.101-28678_101-2867 others(10): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119336632 | |||||
| chr3:119336644
|
A | G | 2 | a0004c0007t0044g0196a0004c0007t0054g0205 | 2 | HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.101-28672A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119336644 | ||||||
| chr3:119336680
|
C | T | 1 | a0001c0001t0024g0243 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.101-28636C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119336680 | ||||||
| chr3:119336681
|
CTATT | C | 27 | a0001c0001t0006g0127a0001c0001t0011g0001a0001c0001t0011g0158others(24): Show | 28 | HG00735.hp1 HG01081.hp2 HG01099.hp1 others(25): Show |
intron_variant | MODIFIER | c.101-28632_101-2862 others(8): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119336681 | |||||
| chr3:119336692
|
A | AT | 10 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(7): Show | 10 | HG00609.hp1 HG02083.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.101-28623dupT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119336692 | |||||
| chr3:119336694
|
A | T | 10 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(7): Show | 10 | HG00609.hp1 HG02083.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.101-28622A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119336694 | ||||||
| chr3:119336695
|
C | A | 10 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(7): Show | 10 | HG00609.hp1 HG02083.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.101-28621C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119336695 | ||||||
| chr3:119336700
|
C | T | 53 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(50): Show | 53 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(50): Show |
intron_variant | MODIFIER | c.101-28616C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119336700 | ||||||
| chr3:119336835
|
G | A | 4 | a0001c0005t0001g0163a0001c0005t0001g0164a0001c0005t0001g0190others(1): Show | 4 | HG01106.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-28481G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119336835 | ||||||
| chr3:119336850
|
T | C | 2 | a0003c0006t0013g0041a0003c0006t0013g0045 | 2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.101-28466T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119336850 | ||||||
| chr3:119336864
|
A | G | 9 | a0001c0001t0020g0043a0001c0001t0029g0042a0001c0001t0050g0177others(6): Show | 9 | HG02015.hp2 HG02451.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.101-28452A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119336864 | ||||||
| chr3:119336903
|
C | T | 155 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(152): Show | 156 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.101-28413C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119336903 | ||||||
| chr3:119337021
|
T | C | 6 | a0001c0001t0006g0092a0001c0001t0007g0202a0001c0001t0007g0251others(3): Show | 6 | HG00438.hp2 HG02523.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.101-28295T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337021 | ||||||
| chr3:119337127
|
T | C | 40 | a0001c0001t0007g0225a0001c0001t0007g0226a0001c0001t0007g0227others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.101-28189T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337127 | ||||||
| chr3:119337141
|
T | G | 1 | a0001c0005t0001g0012 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.101-28175T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337141 | ||||||
| chr3:119337174
|
T | A | 1 | a0001c0004t0021g0059 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.101-28142T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337174 | ||||||
| chr3:119337193
|
G | A | 96 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(93): Show | 96 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.101-28123G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337193 | ||||||
| chr3:119337200
|
C | T | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.101-28116C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337200 | ||||||
| chr3:119337221
|
G | A | 12 | a0001c0001t0020g0043a0001c0001t0029g0042a0001c0001t0050g0177others(9): Show | 12 | HG02015.hp2 HG02451.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-28095G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337221 | ||||||
| chr3:119337236
|
G | C | 4 | a0001c0005t0001g0163a0001c0005t0001g0164a0001c0005t0001g0190others(1): Show | 4 | HG01106.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-28080G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337236 | ||||||
| chr3:119337246
|
C | T | 30 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(27): Show | 30 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.101-28070C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337246 | ||||||
| chr3:119337325
|
T | C | 1 | a0002c0003t0019g0308 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.101-27991T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337325 | ||||||
| chr3:119337331
|
G | A | 55 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(52): Show | 55 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(52): Show |
intron_variant | MODIFIER | c.101-27985G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337331 | ||||||
| chr3:119337382
|
G | A | 3 | a0001c0001t0020g0056a0001c0001t0061g0057a0001c0004t0021g0055 | 3 | HG02486.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.101-27934G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337382 | ||||||
| chr3:119337400
|
T | C | 1 | a0001c0002t0004g0236 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.101-27916T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337400 | ||||||
| chr3:119337415
|
C | T | 1 | a0001c0004t0003g0021 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.101-27901C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337415 | ||||||
| chr3:119337429
|
AG | A | 4 | a0001c0005t0001g0163a0001c0005t0001g0164a0001c0005t0001g0190others(1): Show | 4 | HG01106.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-27886delG | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337429 | ||||||
| chr3:119337430
|
G | A | 1 | a0001c0010t0014g0004 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.101-27886G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337430 | ||||||
| chr3:119337452
|
G | A | 1 | a0001c0004t0032g0071 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.101-27864G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337452 | ||||||
| chr3:119337488
|
C | A | 2 | a0001c0001t0005g0077a0001c0001t0005g0078 | 2 | HG00099.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.101-27828C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337488 | ||||||
| chr3:119337492
|
C | T | 22 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(19): Show | 22 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-27824C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337492 | ||||||
| chr3:119337495
|
A | G | 34 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(31): Show | 34 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.101-27821A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337495 | ||||||
| chr3:119337497
|
T | C | 2 | a0001c0001t0020g0010a0003c0006t0001g0159 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.101-27819T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337497 | ||||||
| chr3:119337515
|
G | A | 2 | a0001c0001t0005g0111a0001c0001t0006g0027 | 2 | HG01993.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.101-27801G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337515 | ||||||
| chr3:119337670
|
T | C | 297 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(294): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.101-27646T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337670 | ||||||
| chr3:119337686
|
C | T | 1 | a0001c0001t0020g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.101-27630C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337686 | ||||||
| chr3:119337744
|
C | G | 11 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(8): Show | 11 | HG00609.hp1 HG02083.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.101-27572C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337744 | ||||||
| chr3:119337834
|
G | A | 1 | a0004c0007t0015g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101-27482G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119337834 | ||||||
| chr3:119338059
|
G | A | 2 | a0002c0003t0002g0152a0003c0006t0056g0011 | 2 | HG01884.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.101-27257G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119338059 | ||||||
| chr3:119338082
|
C | T | 1 | a0001c0001t0017g0303 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.101-27234C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119338082 | ||||||
| chr3:119338083
|
G | A | 1 | a0001c0001t0025g0223 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.101-27233G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119338083 | ||||||
| chr3:119338231
|
G | A | 7 | a0001c0001t0006g0092a0001c0001t0007g0202a0001c0001t0007g0251others(4): Show | 7 | HG00438.hp2 HG01884.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-27085G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119338231 | ||||||
| chr3:119338242
|
G | A | 1 | a0002c0003t0002g0152 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.101-27074G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119338242 | ||||||
| chr3:119338563
|
A | G | 8 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0001t0060g0026others(5): Show | 8 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.101-26753A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119338563 | ||||||
| chr3:119338586
|
C | G | 1 | a0001c0005t0001g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.101-26730C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119338586 | ||||||
| chr3:119338787
|
A | T | 11 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(8): Show | 11 | HG00609.hp1 HG02083.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.101-26529A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119338787 | ||||||
| chr3:119338841
|
A | G | 4 | a0001c0005t0001g0163a0001c0005t0001g0164a0001c0005t0001g0190others(1): Show | 4 | HG01106.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-26475A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119338841 | ||||||
| chr3:119338870
|
G | A | 17 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(14): Show | 17 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-26446G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119338870 | ||||||
| chr3:119339022
|
A | G | 1 | a0002c0003t0002g0060 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.101-26294A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119339022 | ||||||
| chr3:119339204
|
A | G | 2 | a0001c0002t0001g0008a0001c0002t0004g0203 | 2 | HG02976.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.101-26112A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119339204 | ||||||
| chr3:119339308
|
T | C | 1 | a0004c0007t0015g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101-26008T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119339308 | ||||||
| chr3:119339503
|
C | T | 22 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(19): Show | 22 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-25813C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119339503 | ||||||
| chr3:119339511
|
A | G | 20 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(17): Show | 20 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.101-25805A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119339511 | ||||||
| chr3:119339572
|
A | T | 2 | a0004c0007t0044g0196a0004c0007t0054g0205 | 2 | HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.101-25744A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119339572 | ||||||
| chr3:119339678
|
G | A | 43 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(40): Show | 43 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.101-25638G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119339678 | ||||||
| chr3:119339688
|
A | C | 8 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0001t0060g0026others(5): Show | 8 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.101-25628A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119339688 | ||||||
| chr3:119339724
|
CA | C | 22 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(19): Show | 22 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-25584delA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119339724 | |||||
| chr3:119339732
|
A | G | 22 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(19): Show | 22 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-25584A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119339732 | ||||||
| chr3:119339767
|
A | G | 1 | a0004c0007t0015g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101-25549A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119339767 | ||||||
| chr3:119339811
|
C | A | 2 | a0001c0001t0020g0010a0003c0006t0001g0159 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.101-25505C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119339811 | ||||||
| chr3:119339904
|
C | T | 4 | a0001c0005t0001g0163a0001c0005t0001g0164a0001c0005t0001g0190others(1): Show | 4 | HG01106.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-25412C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119339904 | ||||||
| chr3:119339905
|
A | G | 7 | a0001c0001t0006g0092a0001c0001t0007g0202a0001c0001t0007g0251others(4): Show | 7 | HG00438.hp2 HG01884.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-25411A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119339905 | ||||||
| chr3:119340045
|
G | A | 11 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(8): Show | 11 | HG00609.hp1 HG02083.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.101-25271G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119340045 | ||||||
| chr3:119340110
|
A | G | 11 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(8): Show | 11 | HG00609.hp1 HG02083.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.101-25206A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119340110 | ||||||
| chr3:119340256
|
A | G | 7 | a0001c0001t0006g0092a0001c0001t0007g0202a0001c0001t0007g0251others(4): Show | 7 | HG00438.hp2 HG01884.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-25060A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119340256 | ||||||
| chr3:119340272
|
T | C | 1 | a0005c0008t0002g0114 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.101-25044T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119340272 | ||||||
| chr3:119340332
|
A | G | 1 | a0001c0002t0004g0242 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.101-24984A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119340332 | ||||||
| chr3:119340521
|
T | C | 53 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(50): Show | 53 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(50): Show |
intron_variant | MODIFIER | c.101-24795T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119340521 | ||||||
| chr3:119340714
|
C | T | 1 | a0001c0010t0014g0004 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.101-24602C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119340714 | ||||||
| chr3:119340779
|
G | A | 1 | a0001c0010t0014g0004 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.101-24537G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119340779 | ||||||
| chr3:119340790
|
G | T | 1 | a0001c0002t0004g0247 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.101-24526G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119340790 | ||||||
| chr3:119340861
|
A | G | 34 | a0001c0001t0006g0092a0001c0001t0006g0127a0001c0001t0007g0202others(31): Show | 35 | HG00438.hp2 HG00735.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.101-24455A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119340861 | ||||||
| chr3:119340873
|
T | G | 155 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(152): Show | 156 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.101-24443T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119340873 | ||||||
| chr3:119340877
|
G | C | 91 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(88): Show | 91 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.101-24439G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119340877 | ||||||
| chr3:119340929
|
T | C | 155 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(152): Show | 156 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.101-24387T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119340929 | ||||||
| chr3:119341020
|
T | C | 4 | a0001c0005t0001g0163a0001c0005t0001g0164a0001c0005t0001g0190others(1): Show | 4 | HG01106.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-24296T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119341020 | ||||||
| chr3:119341078
|
T | G | 1 | a0001c0004t0003g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.101-24238T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119341078 | ||||||
| chr3:119341233
|
C | A | 135 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(132): Show | 136 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.101-24083C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119341233 | ||||||
| chr3:119341447
|
A | G | 155 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(152): Show | 156 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.101-23869A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119341447 | ||||||
| chr3:119341454
|
T | C | 1 | a0001c0005t0001g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.101-23862T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119341454 | ||||||
| chr3:119341822
|
C | CT | 13 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0001t0060g0026others(10): Show | 13 | HG00639.hp1 HG01106.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.101-23480dupT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119341822 | |||||
| chr3:119341830
|
T | A | 3 | a0001c0001t0011g0183a0001c0004t0051g0157a0009c0017t0019g0185 | 3 | HG03654.hp2 HG03704.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.101-23486T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119341830 | ||||||
| chr3:119341832
|
T | A | 1 | a0001c0002t0001g0074 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.101-23484T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119341832 | ||||||
| chr3:119341836
|
T | A | 2 | a0001c0001t0005g0022a0002c0003t0026g0232 | 2 | HG01975.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.101-23480T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119341836 | ||||||
| chr3:119341846
|
C | A | 4 | a0001c0004t0003g0007a0001c0005t0014g0009a0001c0005t0049g0289others(1): Show | 4 | HG01496.hp1 HG02818.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-23470C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119341846 | ||||||
| chr3:119341893
|
T | A | 1 | a0001c0004t0003g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.101-23423T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119341893 | ||||||
| chr3:119341923
|
C | T | 4 | a0001c0002t0004g0235a0001c0004t0010g0176a0001c0004t0010g0222others(1): Show | 4 | HG00099.hp2 HG01167.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-23393C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119341923 | ||||||
| chr3:119342220
|
C | A | 1 | a0001c0001t0020g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.101-23096C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119342220 | ||||||
| chr3:119342381
|
A | G | 2 | a0001c0010t0014g0004a0003c0006t0056g0011 | 2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.101-22935A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119342381 | ||||||
| chr3:119342725
|
G | C | 9 | a0001c0002t0001g0014a0001c0002t0028g0017a0001c0002t0028g0018others(6): Show | 9 | HG01099.hp2 HG01243.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.101-22591G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119342725 | ||||||
| chr3:119342747
|
C | T | 1 | a0001c0001t0060g0026 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.101-22569C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119342747 | ||||||
| chr3:119342816
|
G | T | 34 | a0001c0001t0006g0092a0001c0001t0006g0127a0001c0001t0007g0202others(31): Show | 35 | HG00438.hp2 HG00735.hp1 HG01081.hp2 others(32): Show |
intron_variant | MODIFIER | c.101-22500G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119342816 | ||||||
| chr3:119342949
|
C | CA | 26 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(23): Show | 26 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.101-22355dupA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119342949 | |||||
| chr3:119342957
|
A | T | 40 | a0001c0001t0006g0092a0001c0001t0006g0127a0001c0001t0007g0202others(37): Show | 41 | HG00438.hp2 HG00735.hp1 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.101-22359A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119342957 | ||||||
| chr3:119343061
|
T | C | 3 | a0001c0001t0020g0056a0001c0001t0061g0057a0001c0004t0021g0055 | 3 | HG02486.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.101-22255T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119343061 | ||||||
| chr3:119343086
|
C | A | 1 | a0001c0004t0032g0071 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.101-22230C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119343086 | ||||||
| chr3:119343234
|
T | A | 4 | a0001c0005t0001g0163a0001c0005t0001g0164a0001c0005t0001g0190others(1): Show | 4 | HG01106.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-22082T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119343234 | ||||||
| chr3:119343418
|
A | G | 1 | a0001c0004t0010g0222 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.101-21898A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119343418 | ||||||
| chr3:119343513
|
A | G | 1 | a0003c0006t0001g0161 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.101-21803A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119343513 | ||||||
| chr3:119343558
|
A | G | 18 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0002t0001g0070others(15): Show | 18 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-21758A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119343558 | ||||||
| chr3:119343690
|
T | C | 4 | a0001c0005t0001g0163a0001c0005t0001g0164a0001c0005t0001g0190others(1): Show | 4 | HG01106.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-21626T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119343690 | ||||||
| chr3:119343793
|
G | T | 7 | a0001c0002t0001g0070a0001c0002t0003g0143a0001c0002t0003g0144others(4): Show | 7 | HG00621.hp2 HG01168.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-21523G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119343793 | ||||||
| chr3:119343795
|
C | T | 19 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(16): Show | 19 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.101-21521C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119343795 | ||||||
| chr3:119343844
|
G | A | 8 | a0001c0001t0006g0092a0001c0001t0007g0202a0001c0001t0007g0251others(5): Show | 8 | HG00438.hp2 HG02523.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.101-21472G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119343844 | ||||||
| chr3:119344050
|
G | GC | 150 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(147): Show | 151 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.101-21265dupC | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119344050 | |||||
| chr3:119344197
|
C | T | 12 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(9): Show | 12 | HG01099.hp1 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-21119C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119344197 | ||||||
| chr3:119344220
|
C | T | 1 | a0001c0004t0003g0038 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.101-21096C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119344220 | ||||||
| chr3:119344221
|
G | A | 1 | a0001c0001t0007g0228 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.101-21095G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119344221 | ||||||
| chr3:119344315
|
G | A | 3 | a0001c0001t0020g0010a0001c0005t0001g0049a0003c0006t0001g0159 | 3 | HG02258.hp1 HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.101-21001G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119344315 | ||||||
| chr3:119344399
|
A | C | 118 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0005g0168others(115): Show | 119 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.101-20917A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119344399 | ||||||
| chr3:119344515
|
G | A | 12 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(9): Show | 12 | HG01099.hp1 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-20801G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119344515 | ||||||
| chr3:119344557
|
T | C | 2 | a0004c0007t0044g0196a0004c0007t0054g0205 | 2 | HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.101-20759T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119344557 | ||||||
| chr3:119344623
|
A | G | 4 | a0001c0004t0003g0038a0001c0004t0003g0039a0001c0004t0003g0040others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-20693A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119344623 | ||||||
| chr3:119344758
|
A | C | 3 | a0001c0001t0020g0056a0001c0001t0061g0057a0001c0004t0021g0055 | 3 | HG02486.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.101-20558A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119344758 | ||||||
| chr3:119344779
|
G | A | 1 | a0001c0001t0017g0302 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.101-20537G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119344779 | ||||||
| chr3:119344864
|
G | A | 2 | a0001c0001t0007g0276a0001c0004t0010g0274 | 2 | HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.101-20452G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119344864 | ||||||
| chr3:119344903
|
G | T | 4 | a0001c0004t0003g0038a0001c0004t0003g0039a0001c0004t0003g0040others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-20413G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119344903 | ||||||
| chr3:119344952
|
G | A | 39 | a0001c0001t0007g0225a0001c0001t0007g0226a0001c0001t0007g0227others(36): Show | 39 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.101-20364G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119344952 | ||||||
| chr3:119344955
|
A | AT | 105 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(102): Show | 106 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.101-20352dupT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119344955 | |||||
| chr3:119344974
|
AT | A | 7 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0001t0060g0026others(4): Show | 7 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-20332delT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119344974 | |||||
| chr3:119345265
|
C | T | 12 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(9): Show | 12 | HG01099.hp1 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-20051C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119345265 | ||||||
| chr3:119345286
|
C | T | 139 | a0001c0001t0005g0058a0001c0001t0005g0168a0001c0001t0005g0169others(136): Show | 140 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.101-20030C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119345286 | ||||||
| chr3:119345296
|
TA | T | 17 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(14): Show | 17 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-20012delA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119345296 | |||||
| chr3:119345335
|
C | T | 1 | a0001c0001t0007g0225 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.101-19981C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119345335 | ||||||
| chr3:119345386
|
C | T | 39 | a0001c0001t0007g0225a0001c0001t0007g0226a0001c0001t0007g0227others(36): Show | 39 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.101-19930C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119345386 | ||||||
| chr3:119345446
|
A | G | 2 | a0001c0001t0006g0109a0001c0004t0003g0120 | 2 | HG02129.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.101-19870A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119345446 | ||||||
| chr3:119345509
|
A | G | 39 | a0001c0001t0007g0225a0001c0001t0007g0226a0001c0001t0007g0227others(36): Show | 39 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.101-19807A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119345509 | ||||||
| chr3:119345609
|
C | T | 1 | a0002c0003t0030g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.101-19707C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119345609 | ||||||
| chr3:119345939
|
G | A | 6 | a0001c0001t0006g0092a0001c0001t0007g0202a0001c0001t0007g0251others(3): Show | 6 | HG00438.hp2 HG02523.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.101-19377G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119345939 | ||||||
| chr3:119345940
|
A | G | 8 | a0001c0001t0006g0092a0001c0001t0007g0202a0001c0001t0007g0251others(5): Show | 8 | HG00438.hp2 HG02523.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.101-19376A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119345940 | ||||||
| chr3:119346179
|
C | T | 24 | a0001c0001t0006g0127a0001c0001t0007g0293a0001c0001t0011g0001others(21): Show | 25 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.101-19137C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119346179 | ||||||
| chr3:119346323
|
A | T | 5 | a0001c0004t0038g0181a0001c0005t0001g0067a0001c0005t0001g0069others(2): Show | 5 | HG02145.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.101-18993A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119346323 | ||||||
| chr3:119346492
|
T | C | 140 | a0001c0001t0005g0058a0001c0001t0005g0168a0001c0001t0005g0169others(137): Show | 141 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.101-18824T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119346492 | ||||||
| chr3:119346601
|
G | T | 166 | a0001c0001t0005g0058a0001c0001t0005g0168a0001c0001t0005g0169others(163): Show | 167 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.101-18715G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119346601 | ||||||
| chr3:119346638
|
T | C | 1 | a0001c0002t0016g0279 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.101-18678T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119346638 | ||||||
| chr3:119346734
|
G | A | 9 | a0001c0001t0006g0092a0001c0001t0007g0202a0001c0001t0007g0251others(6): Show | 9 | HG00438.hp2 HG02523.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.101-18582G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119346734 | ||||||
| chr3:119346767
|
T | A | 1 | a0003c0006t0056g0011 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.101-18549T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119346767 | ||||||
| chr3:119346863
|
C | A | 17 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(14): Show | 17 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-18453C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119346863 | ||||||
| chr3:119346874
|
G | A | 36 | a0001c0001t0007g0225a0001c0001t0007g0226a0001c0001t0007g0227others(33): Show | 36 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(33): Show |
intron_variant | MODIFIER | c.101-18442G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119346874 | ||||||
| chr3:119347081
|
C | T | 1 | a0001c0005t0027g0130 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.101-18235C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119347081 | ||||||
| chr3:119347232
|
C | T | 37 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0007g0275others(34): Show | 37 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.101-18084C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119347232 | ||||||
| chr3:119347388
|
A | G | 35 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(32): Show | 35 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.101-17928A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119347388 | ||||||
| chr3:119347554
|
A | C | 1 | a0013c0020t0013g0051 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.101-17762A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119347554 | ||||||
| chr3:119347579
|
G | A | 7 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0001t0060g0026others(4): Show | 7 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-17737G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119347579 | ||||||
| chr3:119347755
|
A | G | 2 | a0001c0001t0020g0010a0003c0006t0001g0159 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.101-17561A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119347755 | ||||||
| chr3:119347763
|
T | C | 191 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(188): Show | 192 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.101-17553T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119347763 | ||||||
| chr3:119347781
|
G | C | 50 | a0001c0001t0007g0225a0001c0001t0007g0226a0001c0001t0007g0227others(47): Show | 50 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.101-17535G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119347781 | ||||||
| chr3:119347824
|
A | C | 1 | a0002c0003t0009g0248 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.101-17492A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119347824 | ||||||
| chr3:119347925
|
A | G | 2 | a0001c0002t0016g0099a0002c0003t0002g0119 | 2 | NA18953.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.101-17391A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119347925 | ||||||
| chr3:119348257
|
A | C | 85 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(82): Show | 85 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.101-17059A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119348257 | ||||||
| chr3:119348318
|
C | T | 1 | a0010c0016t0004g0166 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.101-16998C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119348318 | ||||||
| chr3:119348374
|
TC | T | 17 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(14): Show | 17 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-16938delC | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119348374 | |||||
| chr3:119348378
|
C | T | 4 | a0001c0005t0001g0163a0001c0005t0001g0164a0001c0005t0001g0190others(1): Show | 4 | HG01106.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-16938C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119348378 | ||||||
| chr3:119348394
|
T | G | 182 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(179): Show | 183 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.101-16922T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119348394 | ||||||
| chr3:119348472
|
G | A | 12 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(9): Show | 12 | HG01099.hp1 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-16844G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119348472 | ||||||
| chr3:119348531
|
A | G | 17 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(14): Show | 17 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-16785A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119348531 | ||||||
| chr3:119348742
|
C | T | 1 | a0001c0001t0008g0199 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.101-16574C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119348742 | ||||||
| chr3:119348827
|
A | G | 83 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(80): Show | 83 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.101-16489A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119348827 | ||||||
| chr3:119348862
|
A | G | 1 | a0002c0003t0043g0210 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.101-16454A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119348862 | ||||||
| chr3:119348866
|
C | T | 1 | a0002c0003t0030g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.101-16450C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119348866 | ||||||
| chr3:119348888
|
A | G | 83 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(80): Show | 83 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.101-16428A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119348888 | ||||||
| chr3:119348919
|
A | G | 7 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0001t0060g0026others(4): Show | 7 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-16397A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119348919 | ||||||
| chr3:119348944
|
C | A | 1 | a0015c0013t0006g0115 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.101-16372C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119348944 | ||||||
| chr3:119348980
|
G | C | 1 | a0002c0003t0030g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.101-16336G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119348980 | ||||||
| chr3:119349313
|
A | T | 50 | a0001c0001t0007g0225a0001c0001t0007g0226a0001c0001t0007g0227others(47): Show | 50 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.101-16003A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119349313 | ||||||
| chr3:119349345
|
G | A | 3 | a0001c0004t0003g0038a0001c0004t0003g0039a0001c0004t0003g0040 | 3 | HG02451.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.101-15971G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119349345 | ||||||
| chr3:119349465
|
A | C | 137 | a0001c0001t0005g0058a0001c0001t0005g0168a0001c0001t0005g0169others(134): Show | 138 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.101-15851A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119349465 | ||||||
| chr3:119349492
|
G | A | 11 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(8): Show | 11 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.101-15824G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119349492 | ||||||
| chr3:119349558
|
G | A | 1 | a0002c0003t0002g0146 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.101-15758G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119349558 | ||||||
| chr3:119349666
|
C | A | 17 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(14): Show | 17 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-15650C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119349666 | ||||||
| chr3:119349742
|
T | C | 13 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(10): Show | 13 | HG00609.hp1 HG01943.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.101-15574T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119349742 | ||||||
| chr3:119349821
|
G | A | 3 | a0001c0001t0020g0056a0001c0001t0061g0057a0001c0004t0021g0055 | 3 | HG02486.hp1 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.101-15495G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119349821 | ||||||
| chr3:119349860
|
G | A | 1 | a0001c0001t0008g0200 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.101-15456G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119349860 | ||||||
| chr3:119349921
|
A | G | 17 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(14): Show | 17 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-15395A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119349921 | ||||||
| chr3:119349930
|
G | A | 2 | a0001c0001t0006g0065a0001c0001t0006g0066 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.101-15386G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119349930 | ||||||
| chr3:119350046
|
T | G | 2 | a0001c0001t0020g0010a0003c0006t0001g0159 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.101-15270T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119350046 | ||||||
| chr3:119350132
|
C | T | 2 | a0001c0001t0020g0010a0003c0006t0001g0159 | 2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.101-15184C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119350132 | ||||||
| chr3:119350146
|
A | G | 17 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(14): Show | 17 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-15170A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119350146 | ||||||
| chr3:119350441
|
C | T | 1 | a0001c0002t0004g0242 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.101-14875C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119350441 | ||||||
| chr3:119350784
|
AGCTGGGG others(6): Show |
A | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-14531_101-1451 others(17): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119350784 | ||||||
| chr3:119350805
|
A | T | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-14511A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119350805 | ||||||
| chr3:119350806
|
C | A | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-14510C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119350806 | ||||||
| chr3:119350807
|
A | C | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-14509A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119350807 | ||||||
| chr3:119350883
|
A | G | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-14433A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119350883 | ||||||
| chr3:119350972
|
A | G | 4 | a0001c0004t0003g0038a0001c0004t0003g0039a0001c0004t0003g0040others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-14344A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119350972 | ||||||
| chr3:119351045
|
C | T | 3 | a0001c0001t0006g0127a0001c0002t0001g0088a0002c0003t0019g0182 | 3 | HG01192.hp1 HG01361.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.101-14271C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119351045 | ||||||
| chr3:119351385
|
T | C | 4 | a0001c0004t0003g0038a0001c0004t0003g0039a0001c0004t0003g0040others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-13931T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119351385 | ||||||
| chr3:119351518
|
A | T | 24 | a0001c0001t0006g0127a0001c0001t0007g0293a0001c0001t0011g0001others(21): Show | 25 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.101-13798A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119351518 | ||||||
| chr3:119351621
|
AG | A | 38 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(35): Show | 39 | HG00609.hp1 HG00639.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.101-13694delG | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119351621 | ||||||
| chr3:119351622
|
G | A | 114 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(111): Show | 114 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.101-13694G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119351622 | ||||||
| chr3:119351670
|
T | C | 82 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(79): Show | 82 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.101-13646T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119351670 | ||||||
| chr3:119351813
|
C | T | 2 | a0001c0005t0001g0163a0001c0005t0001g0164 | 2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.101-13503C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119351813 | ||||||
| chr3:119351940
|
G | T | 18 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0007g0275others(15): Show | 18 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-13376G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119351940 | ||||||
| chr3:119352252
|
T | C | 34 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(31): Show | 35 | HG00609.hp1 HG00639.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.101-13064T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119352252 | ||||||
| chr3:119352376
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.101-12940G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119352376 | ||||||
| chr3:119352379
|
T | A | 162 | a0001c0001t0005g0058a0001c0001t0005g0168a0001c0001t0005g0169others(159): Show | 163 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.101-12937T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119352379 | ||||||
| chr3:119352440
|
C | G | 1 | a0005c0008t0002g0122 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.101-12876C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119352440 | ||||||
| chr3:119352459
|
T | A | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-12857T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119352459 | ||||||
| chr3:119352506
|
G | A | 6 | a0001c0001t0008g0192a0001c0002t0001g0075a0001c0004t0010g0197others(3): Show | 6 | HG00280.hp2 HG01071.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-12810G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119352506 | ||||||
| chr3:119352519
|
G | A | 1 | a0003c0006t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.101-12797G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119352519 | ||||||
| chr3:119352583
|
C | A | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-12733C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119352583 | ||||||
| chr3:119352610
|
CCA | C | 34 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(31): Show | 35 | HG00609.hp1 HG00639.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.101-12689_101-1268 others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119352610 | |||||
| chr3:119352788
|
A | T | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-12528A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119352788 | ||||||
| chr3:119352789
|
G | A | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-12527G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119352789 | ||||||
| chr3:119352790
|
A | G | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-12526A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119352790 | ||||||
| chr3:119352814
|
C | A | 103 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(100): Show | 103 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.101-12502C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119352814 | ||||||
| chr3:119352879
|
T | C | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-12437T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119352879 | ||||||
| chr3:119352880
|
C | T | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-12436C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119352880 | ||||||
| chr3:119352948
|
A | G | 1 | a0001c0001t0018g0209 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.101-12368A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119352948 | ||||||
| chr3:119352995
|
A | T | 1 | a0003c0006t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.101-12321A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119352995 | ||||||
| chr3:119353028
|
G | A | 1 | a0002c0003t0031g0089 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.101-12288G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119353028 | ||||||
| chr3:119353029
|
G | T | 136 | a0001c0001t0005g0058a0001c0001t0005g0168a0001c0001t0005g0169others(133): Show | 137 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.101-12287G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119353029 | ||||||
| chr3:119353118
|
T | C | 4 | a0001c0004t0003g0038a0001c0004t0003g0039a0001c0004t0003g0040others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-12198T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119353118 | ||||||
| chr3:119353200
|
C | T | 4 | a0001c0005t0001g0163a0001c0005t0001g0164a0001c0005t0001g0190others(1): Show | 4 | HG01106.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-12116C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119353200 | ||||||
| chr3:119353290
|
G | A | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.101-12026G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119353290 | ||||||
| chr3:119353407
|
C | T | 85 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(82): Show | 85 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.101-11909C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119353407 | ||||||
| chr3:119353466
|
T | A | 9 | a0001c0001t0006g0092a0001c0001t0007g0202a0001c0001t0007g0251others(6): Show | 9 | HG00438.hp2 HG02523.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.101-11850T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119353466 | ||||||
| chr3:119353514
|
G | A | 32 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(29): Show | 32 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.101-11802G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119353514 | ||||||
| chr3:119353590
|
A | G | 136 | a0001c0001t0005g0058a0001c0001t0005g0168a0001c0001t0005g0169others(133): Show | 137 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.101-11726A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119353590 | ||||||
| chr3:119353635
|
T | A | 1 | a0001c0001t0029g0042 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.101-11681T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119353635 | ||||||
| chr3:119353680
|
C | T | 32 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(29): Show | 32 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.101-11636C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119353680 | ||||||
| chr3:119353725
|
T | C | 85 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(82): Show | 85 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.101-11591T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119353725 | ||||||
| chr3:119353785
|
C | A | 1 | a0002c0003t0002g0063 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.101-11531C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119353785 | ||||||
| chr3:119353787
|
C | CA | 18 | a0001c0001t0005g0077a0001c0001t0007g0275a0001c0002t0001g0070others(15): Show | 18 | HG00099.hp1 HG00621.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.101-11507dupA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119353787 | |||||
| chr3:119353787
|
CA | C | 204 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0096others(201): Show | 205 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.101-11507delA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119353787 | |||||
| chr3:119353787
|
CAA | C | 19 | a0001c0001t0005g0142a0001c0001t0005g0168a0001c0001t0005g0172others(16): Show | 19 | HG00609.hp1 HG01884.hp1 HG01943.hp2 others(16): Show |
intron_variant | MODIFIER | c.101-11508_101-1150 others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119353787 | |||||
| chr3:119353787
|
CAAAA | C | 20 | a0001c0001t0006g0127a0001c0001t0007g0293a0001c0001t0011g0001others(17): Show | 21 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.101-11510_101-1150 others(8): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119353787 | |||||
| chr3:119353812
|
G | T | 3 | a0001c0002t0012g0174a0001c0005t0057g0033a0003c0006t0013g0031 | 3 | HG01099.hp1 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.101-11504G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119353812 | ||||||
| chr3:119353899
|
T | C | 2 | a0004c0007t0044g0196a0004c0007t0054g0205 | 2 | HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.101-11417T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119353899 | ||||||
| chr3:119353990
|
G | C | 1 | a0001c0001t0050g0177 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.101-11326G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119353990 | ||||||
| chr3:119354121
|
C | A | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-11195C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119354121 | ||||||
| chr3:119354122
|
G | A | 21 | a0001c0001t0006g0127a0001c0001t0007g0293a0001c0001t0011g0001others(18): Show | 22 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-11194G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119354122 | ||||||
| chr3:119354259
|
T | A | 85 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(82): Show | 85 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.101-11057T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119354259 | ||||||
| chr3:119354443
|
A | G | 1 | a0002c0003t0062g0093 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.101-10873A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119354443 | ||||||
| chr3:119354476
|
T | TTG | 7 | a0001c0001t0025g0204a0001c0004t0003g0113a0002c0003t0002g0063others(4): Show | 7 | HG00741.hp1 HG00741.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.101-10811_101-1081 others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119354476 | |||||
| chr3:119354476
|
T | TTGTG | 17 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(14): Show | 17 | HG00438.hp2 HG00609.hp1 HG02083.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-10813_101-1081 others(8): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119354476 | |||||
| chr3:119354476
|
TTG | T | 138 | a0001c0001t0005g0022a0001c0001t0005g0087a0001c0001t0005g0096others(135): Show | 140 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.101-10811_101-1081 others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119354476 | |||||
| chr3:119354476
|
TTGTG | T | 85 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(82): Show | 85 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.101-10813_101-1081 others(8): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119354476 | |||||
| chr3:119354476
|
TTGTGTGT others(1): Show |
T | 20 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0007g0241others(17): Show | 20 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.101-10817_101-1081 others(12): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119354476 | |||||
| chr3:119354502
|
G | A | 6 | a0001c0001t0005g0117a0001c0002t0001g0108a0005c0008t0002g0106others(3): Show | 6 | NA18945.hp2 NA19064.hp2 NA19067.hp2 others(3): Show |
intron_variant | MODIFIER | c.101-10814G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119354502 | ||||||
| chr3:119354593
|
C | T | 3 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0259 | 3 | NA18940.hp1 NA18955.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.101-10723C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119354593 | ||||||
| chr3:119354671
|
C | T | 1 | a0002c0003t0030g0149 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.101-10645C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119354671 | ||||||
| chr3:119354678
|
A | AT | 39 | a0001c0001t0006g0092a0001c0001t0006g0094a0001c0001t0006g0127others(36): Show | 40 | HG00438.hp2 HG00639.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.101-10618dupT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119354678 | |||||
| chr3:119354678
|
AT | A | 27 | a0001c0001t0005g0278a0001c0001t0006g0025a0001c0001t0007g0226others(24): Show | 27 | HG01099.hp1 HG01168.hp2 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.101-10618delT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119354678 | |||||
| chr3:119354678
|
ATTT | A | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.101-10620_101-1061 others(7): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119354678 | |||||
| chr3:119354846
|
CTATATT | C | 7 | a0001c0004t0003g0007a0001c0004t0003g0147a0001c0005t0001g0012others(4): Show | 7 | HG01243.hp2 HG01496.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.101-10464_101-1045 others(10): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119354846 | |||||
| chr3:119354887
|
A | AT | 12 | a0001c0001t0046g0307a0001c0002t0012g0174a0001c0005t0001g0029others(9): Show | 12 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-10420dupT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119354887 | |||||
| chr3:119355314
|
A | T | 3 | a0001c0001t0040g0257a0001c0005t0001g0160a0001c0005t0004g0258 | 3 | HG02622.hp2 HG02818.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.101-10002A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119355314 | ||||||
| chr3:119355361
|
A | G | 1 | a0001c0004t0010g0176 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.101-9955A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119355361 | ||||||
| chr3:119355399
|
G | A | 1 | a0001c0001t0024g0243 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.101-9917G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119355399 | ||||||
| chr3:119355470
|
C | CT | 13 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(10): Show | 13 | HG00609.hp1 HG01943.hp2 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.101-9832dupT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119355470 | |||||
| chr3:119355470
|
CT | C | 22 | a0001c0001t0006g0092a0001c0001t0007g0202a0001c0001t0007g0251others(19): Show | 22 | HG00438.hp2 HG02145.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-9832delT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119355470 | |||||
| chr3:119355518
|
G | A | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-9798G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119355518 | ||||||
| chr3:119355575
|
G | A | 7 | a0001c0005t0001g0029a0001c0005t0001g0034a0001c0005t0001g0035others(4): Show | 7 | HG02257.hp1 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.101-9741G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119355575 | ||||||
| chr3:119355594
|
G | A | 1 | a0001c0005t0001g0049 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.101-9722G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119355594 | ||||||
| chr3:119355597
|
A | G | 1 | a0003c0006t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.101-9719A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119355597 | ||||||
| chr3:119355624
|
A | T | 4 | a0001c0001t0020g0010a0001c0001t0020g0056a0001c0001t0061g0057others(1): Show | 4 | HG02486.hp1 HG02970.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-9692A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119355624 | ||||||
| chr3:119355632
|
C | T | 1 | a0001c0001t0008g0229 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.101-9684C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119355632 | ||||||
| chr3:119355634
|
T | C | 66 | a0001c0001t0005g0058a0001c0001t0005g0168a0001c0001t0005g0169others(63): Show | 66 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.101-9682T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119355634 | ||||||
| chr3:119355706
|
A | G | 2 | a0001c0001t0063g0139a0001c0002t0001g0140 | 2 | HG00738.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.101-9610A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119355706 | ||||||
| chr3:119355711
|
G | A | 1 | a0002c0003t0009g0167 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.101-9605G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119355711 | ||||||
| chr3:119355818
|
T | C | 8 | a0001c0005t0001g0029a0001c0005t0001g0034a0001c0005t0001g0035others(5): Show | 8 | HG02257.hp1 HG02280.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.101-9498T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119355818 | ||||||
| chr3:119355993
|
C | T | 4 | a0001c0005t0001g0163a0001c0005t0001g0164a0001c0005t0001g0190others(1): Show | 4 | HG01106.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-9323C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119355993 | ||||||
| chr3:119356010
|
T | G | 18 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0007g0275others(15): Show | 18 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-9306T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119356010 | ||||||
| chr3:119356063
|
C | A | 4 | a0001c0004t0003g0038a0001c0004t0003g0039a0001c0004t0003g0040others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-9253C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119356063 | ||||||
| chr3:119356105
|
C | T | 12 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(9): Show | 12 | HG00609.hp1 HG01943.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-9211C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119356105 | ||||||
| chr3:119356139
|
A | G | 21 | a0001c0001t0006g0127a0001c0001t0007g0293a0001c0001t0011g0001others(18): Show | 22 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-9177A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119356139 | ||||||
| chr3:119356336
|
C | CA | 19 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(16): Show | 19 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.101-8972dupA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119356336 | |||||
| chr3:119356403
|
G | T | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-8913G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119356403 | ||||||
| chr3:119356435
|
A | T | 2 | a0001c0005t0023g0193a0001c0005t0023g0198 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.101-8881A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119356435 | ||||||
| chr3:119356478
|
A | T | 1 | a0003c0006t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.101-8838A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119356478 | ||||||
| chr3:119356615
|
A | T | 1 | a0003c0006t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.101-8701A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119356615 | ||||||
| chr3:119356630
|
C | CA | 27 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(24): Show | 27 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.101-8675dupA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119356630 | |||||
| chr3:119356798
|
T | C | 1 | a0002c0003t0019g0308 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.101-8518T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119356798 | ||||||
| chr3:119356848
|
A | T | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.101-8468A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119356848 | ||||||
| chr3:119356849
|
T | G | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.101-8467T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119356849 | ||||||
| chr3:119356921
|
T | C | 169 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(166): Show | 170 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.101-8395T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119356921 | ||||||
| chr3:119357004
|
C | A | 12 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(9): Show | 12 | HG00609.hp1 HG01943.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-8312C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119357004 | ||||||
| chr3:119357312
|
C | T | 1 | a0001c0001t0020g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.101-8004C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119357312 | ||||||
| chr3:119357368
|
C | T | 1 | a0001c0001t0029g0054 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.101-7948C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119357368 | ||||||
| chr3:119357462
|
CA | C | 25 | a0001c0001t0007g0225a0001c0001t0007g0226a0001c0001t0007g0227others(22): Show | 25 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(22): Show |
intron_variant | MODIFIER | c.101-7853delA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119357462 | ||||||
| chr3:119357465
|
G | A | 1 | a0002c0003t0002g0082 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.101-7851G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119357465 | ||||||
| chr3:119357542
|
T | C | 7 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0001t0060g0026others(4): Show | 7 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-7774T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119357542 | ||||||
| chr3:119357543
|
A | G | 2 | a0001c0005t0023g0193a0001c0005t0023g0198 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.101-7773A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119357543 | ||||||
| chr3:119357614
|
AAAT | A | 12 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(9): Show | 12 | HG00609.hp1 HG01943.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-7693_101-7691d others(5): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119357614 | |||||
| chr3:119357624
|
A | T | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-7692A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119357624 | ||||||
| chr3:119357642
|
C | T | 21 | a0001c0001t0006g0127a0001c0001t0007g0293a0001c0001t0011g0001others(18): Show | 22 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-7674C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119357642 | ||||||
| chr3:119357725
|
G | A | 11 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(8): Show | 11 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.101-7591G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119357725 | ||||||
| chr3:119357753
|
G | A | 2 | a0001c0002t0003g0143a0001c0002t0003g0144 | 2 | NA18955.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.101-7563G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119357753 | ||||||
| chr3:119357844
|
C | A | 21 | a0001c0001t0006g0127a0001c0001t0007g0293a0001c0001t0011g0001others(18): Show | 22 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-7472C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119357844 | ||||||
| chr3:119357887
|
T | G | 4 | a0001c0005t0001g0163a0001c0005t0001g0164a0001c0005t0001g0190others(1): Show | 4 | HG01106.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-7429T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119357887 | ||||||
| chr3:119357975
|
C | G | 2 | a0001c0001t0005g0129a0001c0001t0008g0170 | 2 | NA18946.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.101-7341C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119357975 | ||||||
| chr3:119357984
|
A | G | 18 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0007g0275others(15): Show | 18 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-7332A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119357984 | ||||||
| chr3:119357985
|
A | C | 2 | a0001c0001t0006g0109a0001c0004t0003g0120 | 2 | HG02129.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.101-7331A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119357985 | ||||||
| chr3:119358007
|
A | C | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.101-7309A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119358007 | ||||||
| chr3:119358299
|
A | G | 1 | a0004c0007t0015g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101-7017A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119358299 | ||||||
| chr3:119358543
|
C | T | 1 | a0001c0005t0023g0198 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.101-6773C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119358543 | ||||||
| chr3:119358563
|
A | G | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.101-6753A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119358563 | ||||||
| chr3:119358748
|
A | C | 49 | a0001c0001t0007g0225a0001c0001t0007g0226a0001c0001t0007g0227others(46): Show | 49 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.101-6568A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119358748 | ||||||
| chr3:119358786
|
C | T | 2 | a0001c0005t0001g0029a0001c0005t0001g0036 | 2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.101-6530C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119358786 | ||||||
| chr3:119358821
|
G | A | 4 | a0001c0005t0001g0163a0001c0005t0001g0164a0001c0005t0001g0190others(1): Show | 4 | HG01106.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-6495G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119358821 | ||||||
| chr3:119358850
|
G | C | 18 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0007g0275others(15): Show | 18 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-6466G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119358850 | ||||||
| chr3:119358942
|
A | C | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-6374A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119358942 | ||||||
| chr3:119358955
|
C | T | 12 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(9): Show | 12 | HG00609.hp1 HG01943.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-6361C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119358955 | ||||||
| chr3:119358997
|
T | C | 12 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(9): Show | 12 | HG00609.hp1 HG01943.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-6319T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119358997 | ||||||
| chr3:119359017
|
C | CT | 22 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0005g0121others(19): Show | 22 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-6285dupT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119359017 | |||||
| chr3:119359279
|
A | C | 4 | a0001c0004t0003g0038a0001c0004t0003g0039a0001c0004t0003g0040others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-6037A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119359279 | ||||||
| chr3:119359315
|
C | A | 21 | a0001c0001t0006g0127a0001c0001t0007g0293a0001c0001t0011g0001others(18): Show | 22 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.101-6001C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119359315 | ||||||
| chr3:119359399
|
C | T | 12 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(9): Show | 12 | HG00609.hp1 HG01943.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-5917C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119359399 | ||||||
| chr3:119359435
|
G | A | 1 | a0002c0003t0030g0053 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.101-5881G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119359435 | ||||||
| chr3:119359438
|
G | C | 2 | a0001c0005t0001g0190a0003c0009t0012g0290 | 2 | HG01106.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.101-5878G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119359438 | ||||||
| chr3:119359446
|
GT | G | 7 | a0001c0005t0001g0163a0001c0005t0001g0164a0001c0005t0001g0190others(4): Show | 7 | HG01106.hp2 HG02572.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-5859delT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119359446 | |||||
| chr3:119359447
|
T | G | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-5869T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119359447 | ||||||
| chr3:119359518
|
A | T | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-5798A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119359518 | ||||||
| chr3:119359636
|
G | A | 12 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(9): Show | 12 | HG00609.hp1 HG01943.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-5680G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119359636 | ||||||
| chr3:119359745
|
G | A | 67 | a0001c0001t0006g0092a0001c0001t0007g0202a0001c0001t0007g0225others(64): Show | 67 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.101-5571G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119359745 | ||||||
| chr3:119359754
|
G | A | 2 | a0001c0005t0023g0193a0001c0005t0023g0198 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.101-5562G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119359754 | ||||||
| chr3:119359815
|
G | A | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-5501G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119359815 | ||||||
| chr3:119359860
|
T | TAAAAATC others(5796): Show |
1 | a0001c0004t0010g0274 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.101-5440_101-5439i others(5805): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119359860 | |||||
| chr3:119359860
|
T | TAAAAATC others(5790): Show |
1 | a0001c0001t0007g0276 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.101-5440_101-5439i others(5799): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119359860 | |||||
| chr3:119359865
|
A | T | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-5451A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119359865 | ||||||
| chr3:119359866
|
T | C | 1 | a0001c0001t0046g0307 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.101-5450T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119359866 | ||||||
| chr3:119359881
|
G | A | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.101-5435G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119359881 | ||||||
| chr3:119359904
|
C | T | 4 | a0001c0004t0003g0038a0001c0004t0003g0039a0001c0004t0003g0040others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-5412C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119359904 | ||||||
| chr3:119360019
|
A | T | 1 | a0001c0001t0017g0302 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.101-5297A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119360019 | ||||||
| chr3:119360038
|
C | G | 1 | a0012c0015t0035g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.101-5278C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119360038 | ||||||
| chr3:119360216
|
G | A | 7 | a0001c0001t0007g0296a0001c0001t0008g0215a0001c0001t0008g0216others(4): Show | 7 | HG00738.hp1 HG00741.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-5100G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119360216 | ||||||
| chr3:119360636
|
A | C | 12 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(9): Show | 12 | HG00609.hp1 HG01943.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-4680A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119360636 | ||||||
| chr3:119360722
|
C | A | 3 | a0001c0001t0040g0257a0001c0005t0001g0160a0001c0005t0004g0258 | 3 | HG02622.hp2 HG02818.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.101-4594C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119360722 | ||||||
| chr3:119360853
|
G | C | 12 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(9): Show | 12 | HG00609.hp1 HG01943.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-4463G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119360853 | ||||||
| chr3:119360991
|
C | A | 2 | a0001c0001t0006g0073a0002c0003t0002g0152 | 2 | HG01943.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.101-4325C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119360991 | ||||||
| chr3:119361011
|
C | T | 12 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(9): Show | 12 | HG00609.hp1 HG01943.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.101-4305C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119361011 | ||||||
| chr3:119361329
|
G | C | 1 | a0002c0003t0009g0248 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.101-3987G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119361329 | ||||||
| chr3:119361374
|
C | CT | 42 | a0001c0001t0006g0092a0001c0001t0007g0202a0001c0001t0007g0251others(39): Show | 42 | HG00280.hp2 HG00438.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.101-3923dupT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119361374 | |||||
| chr3:119361374
|
C | CTT | 19 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(16): Show | 19 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.101-3924_101-3923d others(4): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119361374 | |||||
| chr3:119361374
|
C | CTTTT | 11 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(8): Show | 11 | HG00609.hp1 HG01943.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.101-3926_101-3923d others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119361374 | |||||
| chr3:119361420
|
C | G | 1 | a0003c0006t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.101-3896C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119361420 | ||||||
| chr3:119361648
|
C | T | 187 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(184): Show | 188 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.101-3668C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119361648 | ||||||
| chr3:119361681
|
G | A | 1 | a0001c0001t0008g0170 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.101-3635G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119361681 | ||||||
| chr3:119361684
|
C | T | 10 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(7): Show | 10 | HG00609.hp1 HG02083.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-3632C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119361684 | ||||||
| chr3:119361708
|
A | G | 2 | a0001c0002t0004g0247a0002c0003t0009g0220 | 2 | HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.101-3608A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119361708 | ||||||
| chr3:119361714
|
C | T | 3 | a0001c0004t0003g0038a0001c0004t0003g0039a0001c0004t0003g0040 | 3 | HG02451.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.101-3602C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119361714 | ||||||
| chr3:119361756
|
C | G | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.101-3560C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119361756 | ||||||
| chr3:119361998
|
C | T | 1 | a0001c0002t0001g0023 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.101-3318C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119361998 | ||||||
| chr3:119362063
|
G | A | 52 | a0001c0001t0007g0225a0001c0001t0007g0226a0001c0001t0007g0227others(49): Show | 52 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.101-3253G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119362063 | ||||||
| chr3:119362183
|
A | C | 10 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(7): Show | 10 | HG00609.hp1 HG02083.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-3133A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119362183 | ||||||
| chr3:119362259
|
A | G | 3 | a0002c0003t0002g0079a0002c0003t0002g0081a0002c0003t0002g0085 | 3 | NA18945.hp1 NA18957.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.101-3057A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119362259 | ||||||
| chr3:119362551
|
G | A | 3 | a0002c0003t0026g0294a0002c0003t0031g0089a0002c0003t0031g0138 | 3 | HG01496.hp2 HG01978.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.101-2765G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119362551 | ||||||
| chr3:119362712
|
G | A | 1 | a0001c0004t0010g0244 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.101-2604G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119362712 | ||||||
| chr3:119362767
|
T | TA | 20 | a0001c0001t0006g0154a0001c0001t0007g0234a0001c0001t0007g0249others(17): Show | 20 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.101-2533dupA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119362767 | |||||
| chr3:119362792
|
GT | G | 38 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(35): Show | 38 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.101-2523delT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119362792 | ||||||
| chr3:119362793
|
T | G | 28 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(25): Show | 28 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.101-2523T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119362793 | ||||||
| chr3:119362899
|
A | G | 66 | a0001c0001t0005g0058a0001c0001t0005g0168a0001c0001t0005g0169others(63): Show | 66 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.101-2417A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119362899 | ||||||
| chr3:119362929
|
A | G | 34 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(31): Show | 34 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.101-2387A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119362929 | ||||||
| chr3:119362951
|
G | A | 1 | a0003c0006t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.101-2365G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119362951 | ||||||
| chr3:119362984
|
TGTAA | T | 10 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(7): Show | 10 | HG00609.hp1 HG02083.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-2328_101-2325d others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119362984 | |||||
| chr3:119363018
|
G | A | 151 | a0001c0001t0005g0058a0001c0001t0005g0168a0001c0001t0005g0169others(148): Show | 152 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.101-2298G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119363018 | ||||||
| chr3:119363045
|
G | A | 1 | a0001c0005t0001g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.101-2271G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119363045 | ||||||
| chr3:119363122
|
AC | A | 10 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(7): Show | 10 | HG00609.hp1 HG02083.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-2192delC | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 119363122 | |||||
| chr3:119363132
|
G | T | 1 | a0001c0002t0001g0070 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.101-2184G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119363132 | ||||||
| chr3:119363549
|
T | G | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.101-1767T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119363549 | ||||||
| chr3:119363573
|
T | C | 10 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(7): Show | 10 | HG00609.hp1 HG02083.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-1743T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119363573 | ||||||
| chr3:119363597
|
T | G | 2 | a0001c0002t0004g0235a0001c0004t0010g0176 | 2 | HG03669.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.101-1719T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119363597 | ||||||
| chr3:119363780
|
C | A | 2 | a0002c0003t0002g0032a0003c0006t0001g0159 | 2 | HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.101-1536C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119363780 | ||||||
| chr3:119364104
|
C | T | 1 | a0004c0007t0015g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101-1212C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119364104 | ||||||
| chr3:119364122
|
C | T | 1 | a0001c0002t0004g0256 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.101-1194C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119364122 | ||||||
| chr3:119364231
|
G | A | 10 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(7): Show | 10 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.101-1085G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119364231 | ||||||
| chr3:119364243
|
G | A | 1 | a0001c0004t0010g0267 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.101-1073G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119364243 | ||||||
| chr3:119364305
|
C | T | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.101-1011C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119364305 | ||||||
| chr3:119364346
|
A | G | 1 | a0001c0005t0001g0069 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.101-970A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119364346 | ||||||
| chr3:119364602
|
C | T | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.101-714C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119364602 | ||||||
| chr3:119364614
|
G | A | 10 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(7): Show | 10 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.101-702G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119364614 | ||||||
| chr3:119364753
|
G | A | 10 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(7): Show | 10 | HG00609.hp1 HG02083.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.101-563G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119364753 | ||||||
| chr3:119364794
|
T | A | 13 | a0001c0001t0006g0127a0001c0001t0007g0293a0001c0001t0011g0001others(10): Show | 14 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.101-522T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119364794 | ||||||
| chr3:119364859
|
A | G | 18 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0007g0275others(15): Show | 18 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-457A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119364859 | ||||||
| chr3:119364905
|
C | T | 36 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(33): Show | 36 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.101-411C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119364905 | ||||||
| chr3:119364914
|
G | A | 4 | a0001c0004t0003g0038a0001c0004t0003g0039a0001c0004t0003g0040others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-402G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119364914 | ||||||
| chr3:119364930
|
A | C | 152 | a0001c0001t0005g0058a0001c0001t0005g0168a0001c0001t0005g0169others(149): Show | 153 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.101-386A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119364930 | ||||||
| chr3:119364955
|
G | A | 1 | a0002c0003t0002g0118 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.101-361G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119364955 | ||||||
| chr3:119364986
|
C | T | 162 | a0001c0001t0005g0058a0001c0001t0005g0168a0001c0001t0005g0169others(159): Show | 163 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.101-330C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119364986 | ||||||
| chr3:119365022
|
A | G | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.101-294A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119365022 | ||||||
| chr3:119365267
|
G | A | 10 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(7): Show | 10 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.101-49G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119365267 | ||||||
| chr3:119365279
|
C | A | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.101-37C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | 119365279 | ||||||
| chr3:119365484
|
A | G | 15 | a0001c0001t0006g0127a0001c0001t0007g0293a0001c0001t0011g0001others(12): Show | 16 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.203+66A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119365484 | ||||||
| chr3:119365487
|
G | A | 10 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(7): Show | 10 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.203+69G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119365487 | ||||||
| chr3:119365700
|
C | T | 4 | a0001c0004t0003g0038a0001c0004t0003g0039a0001c0004t0003g0040others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.203+282C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119365700 | ||||||
| chr3:119365812
|
G | C | 10 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(7): Show | 10 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.203+394G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119365812 | ||||||
| chr3:119365940
|
A | T | 1 | a0004c0007t0015g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.203+522A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119365940 | ||||||
| chr3:119366052
|
T | G | 1 | a0001c0010t0014g0004 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.203+634T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119366052 | ||||||
| chr3:119366073
|
G | A | 4 | a0001c0005t0001g0163a0001c0005t0001g0164a0001c0005t0001g0190others(1): Show | 4 | HG01106.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.203+655G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119366073 | ||||||
| chr3:119366104
|
T | C | 1 | a0001c0002t0001g0075 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.203+686T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119366104 | ||||||
| chr3:119366137
|
A | G | 210 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(207): Show | 211 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.203+719A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119366137 | ||||||
| chr3:119366144
|
A | G | 12 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(9): Show | 12 | HG00609.hp1 HG01943.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.203+726A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119366144 | ||||||
| chr3:119366279
|
CA | C | 66 | a0001c0001t0005g0058a0001c0001t0005g0168a0001c0001t0005g0169others(63): Show | 66 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.203+869delA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 119366279 | |||||
| chr3:119366299
|
A | G | 1 | a0001c0002t0016g0099 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.203+881A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119366299 | ||||||
| chr3:119366790
|
T | C | 5 | a0001c0004t0038g0181a0001c0005t0001g0067a0001c0005t0001g0069others(2): Show | 5 | HG02145.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.203+1372T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119366790 | ||||||
| chr3:119366958
|
C | G | 1 | a0001c0001t0008g0252 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.204-1414C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119366958 | ||||||
| chr3:119366958
|
C | T | 10 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(7): Show | 10 | HG00609.hp1 HG02083.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.204-1414C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119366958 | ||||||
| chr3:119366999
|
G | A | 2 | a0003c0006t0022g0269a0003c0006t0022g0270 | 2 | HG02055.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.204-1373G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119366999 | ||||||
| chr3:119367091
|
TA | T | 126 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(123): Show | 127 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.204-1266delA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 119367091 | |||||
| chr3:119367091
|
TAA | T | 33 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(30): Show | 33 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.204-1267_204-1266d others(4): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 119367091 | |||||
| chr3:119367759
|
A | C | 52 | a0001c0001t0007g0225a0001c0001t0007g0226a0001c0001t0007g0227others(49): Show | 52 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.204-613A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119367759 | ||||||
| chr3:119367788
|
C | T | 1 | a0001c0005t0001g0165 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.204-584C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119367788 | ||||||
| chr3:119367856
|
C | CA | 5 | a0001c0001t0006g0073a0001c0001t0008g0224a0001c0002t0001g0088others(2): Show | 5 | HG01943.hp2 HG02451.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.204-508dupA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 119367856 | |||||
| chr3:119367856
|
C | CAA | 14 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(11): Show | 14 | HG00609.hp1 HG02083.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.204-509_204-508dup others(2): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 119367856 | |||||
| chr3:119367864
|
AG | A | 20 | a0001c0001t0006g0065a0001c0001t0007g0234a0001c0001t0007g0249others(17): Show | 20 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.204-507delG | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119367864 | ||||||
| chr3:119367865
|
G | A | 60 | a0001c0001t0005g0058a0001c0001t0005g0168a0001c0001t0005g0169others(57): Show | 61 | HG00609.hp1 HG00639.hp2 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.204-507G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119367865 | ||||||
| chr3:119367865
|
G | GA | 9 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(6): Show | 9 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.204-492dupA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 119367865 | |||||
| chr3:119367927
|
A | T | 3 | a0001c0002t0016g0097a0001c0002t0016g0098a0001c0002t0016g0099 | 3 | NA18953.hp2 NA18998.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.204-445A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119367927 | ||||||
| chr3:119367962
|
C | T | 32 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(29): Show | 32 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.204-410C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119367962 | ||||||
| chr3:119367989
|
C | T | 35 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(32): Show | 35 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.204-383C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119367989 | ||||||
| chr3:119368123
|
G | A | 3 | a0001c0001t0005g0022a0001c0002t0004g0230a0001c0002t0033g0231 | 3 | HG01975.hp2 NA18612.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.204-249G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 2/11 | chr3 | 119368123 | ||||||
| chr3:119368737
|
G | A | 1 | a0001c0010t0014g0004 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.348+221G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119368737 | ||||||
| chr3:119368851
|
A | G | 2 | a0004c0007t0044g0196a0004c0007t0054g0205 | 2 | HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.348+335A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119368851 | ||||||
| chr3:119368871
|
A | G | 33 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(30): Show | 33 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.348+355A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119368871 | ||||||
| chr3:119368935
|
T | G | 187 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(184): Show | 188 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.348+419T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119368935 | ||||||
| chr3:119368962
|
G | A | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.348+446G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119368962 | ||||||
| chr3:119368987
|
T | G | 64 | a0001c0001t0005g0058a0001c0001t0005g0168a0001c0001t0005g0169others(61): Show | 65 | HG00609.hp1 HG00639.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.348+471T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119368987 | ||||||
| chr3:119368996
|
G | A | 14 | a0001c0001t0006g0127a0001c0001t0007g0293a0001c0001t0011g0001others(11): Show | 15 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.348+480G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119368996 | ||||||
| chr3:119369102
|
T | C | 6 | a0001c0001t0008g0224a0001c0001t0020g0043a0001c0001t0029g0042others(3): Show | 6 | HG02015.hp2 HG02683.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+586T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119369102 | ||||||
| chr3:119369236
|
T | C | 3 | a0001c0005t0023g0193a0001c0005t0023g0198a0002c0018t0019g0284 | 3 | HG02647.hp1 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.348+720T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119369236 | ||||||
| chr3:119369259
|
A | G | 3 | a0001c0002t0012g0206a0002c0003t0002g0032a0003c0006t0001g0159 | 3 | HG02257.hp2 HG02451.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.348+743A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119369259 | ||||||
| chr3:119369404
|
T | A | 1 | a0001c0004t0003g0076 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.348+888T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119369404 | ||||||
| chr3:119369467
|
G | A | 1 | a0001c0002t0001g0101 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.348+951G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119369467 | ||||||
| chr3:119369522
|
T | C | 1 | a0003c0006t0056g0011 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.348+1006T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119369522 | ||||||
| chr3:119369541
|
T | C | 10 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(7): Show | 10 | HG00609.hp1 HG02083.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+1025T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119369541 | ||||||
| chr3:119369620
|
G | T | 10 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(7): Show | 10 | HG00609.hp1 HG02083.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+1104G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119369620 | ||||||
| chr3:119369660
|
C | A | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.348+1144C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119369660 | ||||||
| chr3:119369696
|
A | T | 10 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(7): Show | 10 | HG00609.hp1 HG02083.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+1180A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119369696 | ||||||
| chr3:119369891
|
T | C | 10 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(7): Show | 10 | HG00609.hp1 HG02083.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+1375T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119369891 | ||||||
| chr3:119369953
|
T | TA | 13 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0007g0275others(10): Show | 13 | HG00099.hp1 HG00323.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.348+1447dupA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119369953 | |||||
| chr3:119369953
|
TA | T | 19 | a0001c0001t0006g0092a0001c0001t0007g0202a0001c0001t0007g0251others(16): Show | 19 | HG00438.hp2 HG00621.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.348+1447delA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119369953 | |||||
| chr3:119370064
|
G | T | 10 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(7): Show | 10 | HG00609.hp1 HG02083.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+1548G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119370064 | ||||||
| chr3:119370102
|
G | A | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.348+1586G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119370102 | ||||||
| chr3:119370111
|
C | A | 2 | a0001c0002t0028g0017a0001c0002t0028g0018 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.348+1595C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119370111 | ||||||
| chr3:119370241
|
C | G | 7 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0001t0060g0026others(4): Show | 7 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.348+1725C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119370241 | ||||||
| chr3:119370338
|
A | C | 1 | a0002c0003t0002g0060 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.348+1822A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119370338 | ||||||
| chr3:119370434
|
T | G | 1 | a0001c0002t0004g0230 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.348+1918T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119370434 | ||||||
| chr3:119370493
|
C | T | 10 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(7): Show | 10 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.348+1977C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119370493 | ||||||
| chr3:119370583
|
AAC | A | 10 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(7): Show | 10 | HG00609.hp1 HG02083.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.348+2078_348+2079d others(4): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119370583 | |||||
| chr3:119370691
|
A | C | 1 | a0001c0002t0004g0235 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.348+2175A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119370691 | ||||||
| chr3:119370843
|
T | C | 3 | a0001c0001t0008g0180a0001c0004t0003g0021a0002c0003t0009g0201 | 3 | NA18952.hp1 NA18985.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.348+2327T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119370843 | ||||||
| chr3:119370862
|
A | G | 1 | a0001c0001t0007g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.348+2346A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119370862 | ||||||
| chr3:119370923
|
A | G | 62 | a0001c0001t0005g0058a0001c0001t0005g0168a0001c0001t0005g0169others(59): Show | 63 | HG00609.hp1 HG00639.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.348+2407A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119370923 | ||||||
| chr3:119371036
|
C | A | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.348+2520C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119371036 | ||||||
| chr3:119371047
|
C | T | 7 | a0001c0001t0018g0207a0001c0001t0018g0208a0001c0001t0020g0010others(4): Show | 7 | HG02258.hp1 HG02486.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.348+2531C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119371047 | ||||||
| chr3:119371478
|
A | G | 116 | a0001c0001t0005g0058a0001c0001t0005g0168a0001c0001t0005g0169others(113): Show | 117 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.348+2962A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119371478 | ||||||
| chr3:119371560
|
C | T | 2 | a0001c0005t0023g0193a0001c0005t0023g0198 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.348+3044C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119371560 | ||||||
| chr3:119371620
|
C | A | 30 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(27): Show | 30 | HG01099.hp2 HG01243.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.348+3104C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119371620 | ||||||
| chr3:119371647
|
A | G | 1 | a0011c0019t0005g0155 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.348+3131A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119371647 | ||||||
| chr3:119371697
|
A | T | 1 | a0001c0002t0012g0174 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.348+3181A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119371697 | ||||||
| chr3:119371840
|
A | T | 18 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0007g0275others(15): Show | 18 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.348+3324A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119371840 | ||||||
| chr3:119372009
|
T | C | 1 | a0001c0001t0020g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.348+3493T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119372009 | ||||||
| chr3:119372096
|
C | A | 4 | a0001c0004t0003g0038a0001c0004t0003g0039a0001c0004t0003g0040others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+3580C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119372096 | ||||||
| chr3:119372165
|
C | T | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.348+3649C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119372165 | ||||||
| chr3:119372280
|
C | CT | 8 | a0001c0001t0005g0117a0001c0001t0005g0156a0001c0001t0006g0094others(5): Show | 8 | HG00735.hp2 HG02055.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.348+3784dupT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119372280 | |||||
| chr3:119372280
|
CT | C | 17 | a0001c0001t0018g0207a0001c0001t0020g0010a0001c0001t0020g0056others(14): Show | 17 | HG01884.hp2 HG02258.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.348+3784delT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119372280 | |||||
| chr3:119372280
|
CTT | C | 45 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(42): Show | 45 | HG00438.hp2 HG01099.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.348+3783_348+3784d others(4): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119372280 | |||||
| chr3:119372280
|
CTTT | C | 33 | a0001c0001t0006g0127a0001c0001t0007g0234a0001c0001t0007g0249others(30): Show | 34 | HG00408.hp2 HG00609.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.348+3782_348+3784d others(5): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119372280 | |||||
| chr3:119372359
|
C | T | 10 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(7): Show | 10 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.348+3843C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119372359 | ||||||
| chr3:119372425
|
A | C | 2 | a0004c0007t0044g0196a0004c0007t0054g0205 | 2 | HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.348+3909A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119372425 | ||||||
| chr3:119372441
|
G | A | 30 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(27): Show | 30 | HG01099.hp2 HG01243.hp2 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.348+3925G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119372441 | ||||||
| chr3:119372472
|
G | A | 4 | a0001c0004t0003g0038a0001c0004t0003g0039a0001c0004t0003g0040others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.348+3956G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119372472 | ||||||
| chr3:119372511
|
G | A | 14 | a0001c0001t0006g0127a0001c0001t0007g0293a0001c0001t0011g0001others(11): Show | 15 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.348+3995G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119372511 | ||||||
| chr3:119372578
|
C | T | 1 | a0001c0002t0001g0080 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.348+4062C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119372578 | ||||||
| chr3:119372583
|
T | C | 1 | a0001c0001t0020g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.348+4067T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119372583 | ||||||
| chr3:119372707
|
C | A | 1 | a0004c0007t0015g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.348+4191C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119372707 | ||||||
| chr3:119372866
|
C | G | 1 | a0002c0003t0002g0090 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.348+4350C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119372866 | ||||||
| chr3:119372965
|
C | A | 10 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(7): Show | 10 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.348+4449C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119372965 | ||||||
| chr3:119373434
|
CT | C | 140 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(137): Show | 140 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.348+4928delT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119373434 | |||||
| chr3:119373442
|
T | G | 2 | a0001c0002t0001g0075a0005c0008t0002g0107 | 2 | HG01071.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.348+4926T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119373442 | ||||||
| chr3:119373444
|
TG | T | 21 | a0001c0001t0006g0092a0001c0001t0007g0202a0001c0001t0007g0251others(18): Show | 21 | HG00438.hp2 HG02258.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.348+4929delG | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119373444 | ||||||
| chr3:119373445
|
G | T | 13 | a0001c0001t0006g0127a0001c0001t0007g0293a0001c0001t0011g0001others(10): Show | 14 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.348+4929G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119373445 | ||||||
| chr3:119373468
|
T | G | 1 | a0001c0001t0017g0175 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.348+4952T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119373468 | ||||||
| chr3:119373477
|
T | G | 4 | a0001c0005t0001g0163a0001c0005t0001g0164a0001c0005t0001g0190others(1): Show | 4 | HG01106.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.348+4961T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119373477 | ||||||
| chr3:119373556
|
C | T | 3 | a0001c0002t0004g0247a0002c0003t0009g0220a0010c0016t0004g0166 | 3 | HG00735.hp2 HG02615.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.348+5040C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119373556 | ||||||
| chr3:119373612
|
C | T | 17 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0007g0275others(14): Show | 17 | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.348+5096C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119373612 | ||||||
| chr3:119373760
|
A | G | 165 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(162): Show | 166 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.348+5244A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119373760 | ||||||
| chr3:119374093
|
A | G | 1 | a0001c0005t0014g0062 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.348+5577A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119374093 | ||||||
| chr3:119374101
|
G | T | 5 | a0001c0004t0038g0181a0001c0005t0001g0067a0001c0005t0001g0069others(2): Show | 5 | HG02145.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+5585G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119374101 | ||||||
| chr3:119374329
|
G | A | 18 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.348+5813G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119374329 | ||||||
| chr3:119374416
|
G | A | 6 | a0001c0001t0006g0094a0001c0001t0006g0109a0001c0004t0003g0095others(3): Show | 6 | HG02129.hp2 HG03834.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.348+5900G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119374416 | ||||||
| chr3:119374449
|
TC | T | 90 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(87): Show | 91 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.348+5934delC | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119374449 | ||||||
| chr3:119374467
|
C | T | 10 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(7): Show | 10 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.348+5951C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119374467 | ||||||
| chr3:119374580
|
G | A | 1 | a0003c0006t0056g0011 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.348+6064G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119374580 | ||||||
| chr3:119374637
|
G | C | 83 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0005g0168others(80): Show | 83 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.348+6121G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119374637 | ||||||
| chr3:119374715
|
C | A | 1 | a0001c0001t0020g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.349-6189C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119374715 | ||||||
| chr3:119374924
|
G | A | 2 | a0001c0005t0023g0193a0001c0005t0023g0198 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.349-5980G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119374924 | ||||||
| chr3:119375140
|
T | C | 2 | a0001c0005t0012g0285a0001c0005t0012g0287 | 2 | HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.349-5764T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119375140 | ||||||
| chr3:119375237
|
C | T | 39 | a0001c0001t0007g0225a0001c0001t0007g0226a0001c0001t0007g0227others(36): Show | 39 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.349-5667C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119375237 | ||||||
| chr3:119375367
|
T | C | 202 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(199): Show | 203 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.349-5537T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119375367 | ||||||
| chr3:119375382
|
G | A | 14 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(11): Show | 14 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.349-5522G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119375382 | ||||||
| chr3:119375392
|
C | T | 12 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(9): Show | 12 | HG00609.hp1 HG02083.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.349-5512C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119375392 | ||||||
| chr3:119375438
|
A | G | 1 | a0001c0001t0005g0156 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.349-5466A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119375438 | ||||||
| chr3:119375441
|
T | C | 48 | a0001c0001t0005g0058a0001c0001t0006g0065a0001c0001t0006g0066others(45): Show | 49 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.349-5463T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119375441 | ||||||
| chr3:119375532
|
T | C | 1 | a0001c0005t0001g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.349-5372T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119375532 | ||||||
| chr3:119375534
|
G | C | 1 | a0001c0002t0001g0074 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.349-5370G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119375534 | ||||||
| chr3:119375565
|
A | G | 12 | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(9): Show | 12 | HG00609.hp1 HG02083.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.349-5339A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119375565 | ||||||
| chr3:119375809
|
T | C | 12 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(9): Show | 12 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.349-5095T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119375809 | ||||||
| chr3:119375843
|
A | C | 1 | a0003c0006t0056g0011 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.349-5061A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119375843 | ||||||
| chr3:119375909
|
T | C | 2 | a0001c0001t0006g0131a0002c0003t0002g0119 | 2 | NA18953.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.349-4995T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119375909 | ||||||
| chr3:119375942
|
C | T | 21 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0007g0234others(18): Show | 21 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(18): Show |
intron_variant | MODIFIER | c.349-4962C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119375942 | ||||||
| chr3:119375990
|
T | A | 22 | a0001c0001t0008g0192a0001c0001t0008g0215a0001c0001t0008g0216others(19): Show | 22 | HG00280.hp2 HG00741.hp1 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.349-4914T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119375990 | ||||||
| chr3:119376024
|
T | C | 1 | a0001c0005t0001g0020 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.349-4880T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119376024 | ||||||
| chr3:119376033
|
G | A | 2 | a0001c0010t0014g0004a0003c0009t0004g0261 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.349-4871G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119376033 | ||||||
| chr3:119376067
|
C | T | 4 | a0001c0001t0020g0010a0001c0005t0001g0190a0003c0009t0012g0290others(1): Show | 4 | HG01106.hp2 HG02970.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.349-4837C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119376067 | ||||||
| chr3:119376104
|
G | GTT | 41 | a0001c0001t0008g0192a0001c0001t0008g0215a0001c0001t0008g0216others(38): Show | 41 | HG00280.hp2 HG00621.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.349-4798_349-4797d others(4): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119376104 | |||||
| chr3:119376108
|
C | A | 41 | a0001c0001t0008g0192a0001c0001t0008g0215a0001c0001t0008g0216others(38): Show | 41 | HG00280.hp2 HG00621.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.349-4796C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119376108 | ||||||
| chr3:119376109
|
C | T | 2 | a0004c0007t0044g0196a0004c0007t0054g0205 | 2 | HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.349-4795C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119376109 | ||||||
| chr3:119376209
|
C | T | 44 | a0001c0001t0006g0073a0001c0001t0008g0192a0001c0001t0008g0215others(41): Show | 44 | HG00280.hp2 HG00621.hp2 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.349-4695C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119376209 | ||||||
| chr3:119376211
|
A | G | 1 | a0002c0003t0002g0082 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.349-4693A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119376211 | ||||||
| chr3:119376247
|
G | A | 1 | a0001c0002t0001g0171 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.349-4657G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119376247 | ||||||
| chr3:119376254
|
T | G | 1 | a0003c0006t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.349-4650T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119376254 | ||||||
| chr3:119376346
|
G | A | 15 | a0001c0001t0005g0172a0001c0002t0012g0174a0001c0005t0001g0029others(12): Show | 15 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.349-4558G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119376346 | ||||||
| chr3:119376387
|
G | C | 116 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0005g0278others(113): Show | 118 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.349-4517G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119376387 | ||||||
| chr3:119376580
|
C | T | 205 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(202): Show | 207 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(204): Show |
intron_variant | MODIFIER | c.349-4324C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119376580 | ||||||
| chr3:119376618
|
C | CCT | 5 | a0001c0001t0029g0042a0001c0010t0014g0004a0003c0006t0022g0269others(2): Show | 5 | HG02055.hp2 HG02280.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.349-4283_349-4282d others(4): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119376618 | |||||
| chr3:119376758
|
CA | C | 97 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0005g0278others(94): Show | 98 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.349-4132delA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119376758 | |||||
| chr3:119376758
|
CAA | C | 29 | a0001c0001t0008g0192a0001c0001t0008g0215a0001c0001t0008g0216others(26): Show | 29 | HG00280.hp2 HG00741.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.349-4133_349-4132d others(4): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119376758 | |||||
| chr3:119376758
|
CAAA | C | 14 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(11): Show | 14 | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.349-4134_349-4132d others(5): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119376758 | |||||
| chr3:119376806
|
T | C | 12 | a0001c0001t0007g0293a0001c0001t0011g0001a0001c0001t0011g0158others(9): Show | 13 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.349-4098T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119376806 | ||||||
| chr3:119376902
|
A | C | 1 | a0001c0002t0012g0238 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.349-4002A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119376902 | ||||||
| chr3:119376965
|
A | G | 51 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0007g0234others(48): Show | 52 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.349-3939A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119376965 | ||||||
| chr3:119377049
|
T | C | 21 | a0001c0001t0020g0056a0001c0001t0039g0260a0001c0001t0061g0057others(18): Show | 21 | HG00621.hp2 HG01099.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.349-3855T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119377049 | ||||||
| chr3:119377102
|
A | G | 51 | a0001c0001t0005g0278a0001c0001t0006g0065a0001c0001t0006g0066others(48): Show | 52 | HG00280.hp1 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.349-3802A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119377102 | ||||||
| chr3:119377186
|
G | A | 1 | a0001c0001t0020g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.349-3718G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119377186 | ||||||
| chr3:119377230
|
GA | G | 24 | a0001c0001t0005g0058a0001c0001t0006g0092a0001c0001t0007g0202others(21): Show | 24 | HG00438.hp2 HG01255.hp2 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.349-3671delA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119377230 | |||||
| chr3:119377306
|
G | A | 2 | a0001c0002t0012g0206a0002c0003t0002g0032 | 2 | HG02257.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.349-3598G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119377306 | ||||||
| chr3:119377321
|
A | G | 1 | a0001c0002t0037g0214 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.349-3583A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119377321 | ||||||
| chr3:119377479
|
G | T | 1 | a0001c0005t0004g0253 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.349-3425G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119377479 | ||||||
| chr3:119377521
|
T | C | 25 | a0001c0001t0005g0058a0001c0001t0006g0092a0001c0001t0007g0202others(22): Show | 25 | HG00438.hp2 HG01255.hp2 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.349-3383T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119377521 | ||||||
| chr3:119377540
|
A | T | 2 | a0001c0005t0023g0193a0001c0005t0023g0198 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.349-3364A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119377540 | ||||||
| chr3:119377576
|
C | T | 1 | a0001c0001t0007g0241 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.349-3328C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119377576 | ||||||
| chr3:119377604
|
G | C | 6 | a0001c0001t0018g0207a0001c0001t0018g0208a0001c0001t0020g0010others(3): Show | 6 | HG01106.hp2 HG02970.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.349-3300G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119377604 | ||||||
| chr3:119377608
|
C | G | 5 | a0001c0002t0012g0206a0001c0005t0001g0163a0001c0005t0001g0164others(2): Show | 5 | HG02257.hp2 HG02451.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-3296C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119377608 | ||||||
| chr3:119377725
|
T | G | 1 | a0001c0001t0020g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.349-3179T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119377725 | ||||||
| chr3:119377747
|
C | T | 19 | a0001c0001t0008g0192a0001c0001t0008g0215a0001c0001t0008g0216others(16): Show | 19 | HG00280.hp1 HG00280.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.349-3157C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119377747 | ||||||
| chr3:119377752
|
C | CT | 24 | a0001c0001t0005g0058a0001c0001t0006g0092a0001c0001t0008g0224others(21): Show | 24 | HG00438.hp2 HG01255.hp2 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.349-3138dupT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119377752 | |||||
| chr3:119377752
|
CT | C | 10 | a0001c0001t0005g0022a0001c0001t0007g0226a0001c0001t0007g0228others(7): Show | 10 | HG01099.hp1 HG01256.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.349-3138delT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119377752 | |||||
| chr3:119377810
|
TA | T | 109 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0005g0278others(106): Show | 111 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.349-3090delA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119377810 | |||||
| chr3:119377940
|
G | A | 13 | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0035others(10): Show | 13 | HG01099.hp1 HG02257.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.349-2964G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119377940 | ||||||
| chr3:119377981
|
C | T | 1 | a0002c0003t0031g0089 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.349-2923C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119377981 | ||||||
| chr3:119378016
|
C | T | 3 | a0001c0001t0006g0092a0001c0002t0016g0133a0002c0003t0019g0308 | 3 | HG00438.hp2 HG02523.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.349-2888C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119378016 | ||||||
| chr3:119378132
|
T | C | 1 | a0001c0002t0016g0279 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.349-2772T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119378132 | ||||||
| chr3:119378182
|
C | G | 21 | a0001c0001t0020g0056a0001c0001t0039g0260a0001c0001t0061g0057others(18): Show | 21 | HG00621.hp2 HG01099.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.349-2722C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119378182 | ||||||
| chr3:119378258
|
T | C | 1 | a0003c0006t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.349-2646T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119378258 | ||||||
| chr3:119378274
|
A | C | 5 | a0001c0004t0038g0181a0001c0005t0001g0067a0001c0005t0001g0069others(2): Show | 5 | HG02145.hp1 HG02630.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-2630A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119378274 | ||||||
| chr3:119378278
|
C | T | 5 | a0001c0001t0006g0073a0001c0001t0025g0204a0001c0005t0048g0304others(2): Show | 5 | HG01943.hp2 HG02083.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-2626C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119378278 | ||||||
| chr3:119378299
|
G | A | 1 | a0003c0009t0004g0261 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.349-2605G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119378299 | ||||||
| chr3:119378386
|
A | T | 1 | a0002c0003t0002g0085 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.349-2518A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119378386 | ||||||
| chr3:119378413
|
C | T | 2 | a0001c0010t0014g0004a0003c0009t0004g0261 | 2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.349-2491C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119378413 | ||||||
| chr3:119378430
|
G | A | 1 | a0003c0006t0056g0011 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.349-2474G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119378430 | ||||||
| chr3:119378434
|
C | T | 2 | a0001c0002t0001g0074a0003c0006t0056g0011 | 2 | HG01884.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.349-2470C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119378434 | ||||||
| chr3:119378487
|
T | C | 1 | a0003c0006t0013g0006 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.349-2417T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119378487 | ||||||
| chr3:119378505
|
T | C | 2 | a0001c0001t0006g0065a0001c0001t0006g0066 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.349-2399T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119378505 | ||||||
| chr3:119378701
|
T | C | 160 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0005g0121others(157): Show | 162 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.349-2203T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119378701 | ||||||
| chr3:119378709
|
C | T | 1 | a0001c0004t0010g0267 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.349-2195C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119378709 | ||||||
| chr3:119378742
|
C | T | 2 | a0001c0001t0018g0208a0001c0001t0024g0243 | 2 | HG04228.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.349-2162C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119378742 | ||||||
| chr3:119379005
|
G | A | 5 | a0001c0010t0014g0004a0003c0009t0004g0261a0003c0009t0012g0290others(2): Show | 5 | HG01106.hp2 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.349-1899G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119379005 | ||||||
| chr3:119379353
|
T | C | 1 | a0003c0006t0056g0011 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.349-1551T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119379353 | ||||||
| chr3:119379480
|
T | A | 1 | a0001c0001t0005g0156 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.349-1424T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119379480 | ||||||
| chr3:119379494
|
G | A | 33 | a0001c0001t0005g0058a0001c0001t0005g0169a0001c0001t0006g0092others(30): Show | 33 | HG00438.hp2 HG00735.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.349-1410G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119379494 | ||||||
| chr3:119379524
|
C | T | 1 | a0001c0001t0005g0022 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.349-1380C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119379524 | ||||||
| chr3:119379543
|
C | T | 3 | a0001c0004t0003g0038a0001c0004t0003g0039a0001c0004t0003g0040 | 3 | HG02451.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.349-1361C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119379543 | ||||||
| chr3:119379590
|
AAATT | A | 58 | a0001c0001t0005g0096a0001c0001t0005g0121a0001c0001t0005g0278others(55): Show | 59 | HG00323.hp1 HG00597.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.349-1307_349-1304d others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119379590 | |||||
| chr3:119379607
|
C | T | 3 | a0001c0002t0001g0008a0001c0002t0004g0203a0001c0004t0021g0055 | 3 | HG02976.hp2 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.349-1297C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119379607 | ||||||
| chr3:119379642
|
G | A | 4 | a0001c0001t0020g0010a0001c0002t0012g0206a0002c0003t0002g0032others(1): Show | 4 | HG02257.hp2 HG02451.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.349-1262G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119379642 | ||||||
| chr3:119379763
|
G | GA | 13 | a0001c0001t0005g0156a0001c0001t0007g0293a0001c0001t0011g0001others(10): Show | 14 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.349-1134dupA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119379763 | |||||
| chr3:119379775
|
T | C | 1 | a0001c0004t0003g0147 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.349-1129T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119379775 | ||||||
| chr3:119379829
|
T | C | 169 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0005g0096others(166): Show | 171 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.349-1075T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119379829 | ||||||
| chr3:119380176
|
A | G | 1 | a0003c0006t0056g0011 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.349-728A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119380176 | ||||||
| chr3:119380202
|
A | G | 216 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(213): Show | 218 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.349-702A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119380202 | ||||||
| chr3:119380207
|
A | T | 9 | a0001c0002t0001g0014a0001c0002t0028g0017a0001c0002t0028g0018others(6): Show | 9 | HG01099.hp2 HG01243.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.349-697A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119380207 | ||||||
| chr3:119380347
|
C | T | 21 | a0001c0001t0020g0056a0001c0001t0039g0260a0001c0001t0061g0057others(18): Show | 21 | HG00621.hp2 HG01099.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.349-557C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119380347 | ||||||
| chr3:119380385
|
T | C | 1 | a0004c0007t0044g0196 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.349-519T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119380385 | ||||||
| chr3:119380404
|
TATTC | T | 126 | a0001c0001t0005g0096a0001c0001t0005g0121a0001c0001t0005g0278others(123): Show | 128 | HG00323.hp1 HG00597.hp1 HG00621.hp1 others(125): Show |
intron_variant | MODIFIER | c.349-477_349-474del others(4): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 119380404 | |||||
| chr3:119380456
|
C | T | 9 | a0001c0001t0045g0286a0001c0001t0052g0283a0001c0001t0060g0026others(6): Show | 9 | HG02559.hp1 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.349-448C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119380456 | ||||||
| chr3:119380513
|
G | A | 20 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0007g0234others(17): Show | 20 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(17): Show |
intron_variant | MODIFIER | c.349-391G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119380513 | ||||||
| chr3:119380603
|
C | T | 3 | a0001c0010t0014g0004a0003c0009t0004g0261a0003c0009t0012g0290 | 3 | HG01106.hp2 HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.349-301C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119380603 | ||||||
| chr3:119380751
|
A | G | 215 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(212): Show | 217 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.349-153A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119380751 | ||||||
| chr3:119380791
|
C | T | 11 | a0001c0001t0007g0293a0001c0001t0011g0001a0001c0001t0011g0158others(8): Show | 12 | HG00639.hp2 HG00735.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.349-113C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | chr3 | 119380791 | ||||||
| chr3:119381176
|
G | A | 5 | a0001c0004t0003g0038a0001c0004t0003g0039a0001c0004t0003g0040others(2): Show | 5 | HG02451.hp2 HG02572.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.431+190G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381176 | ||||||
| chr3:119381242
|
A | G | 2 | a0004c0007t0044g0196a0004c0007t0054g0205 | 2 | HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.431+256A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381242 | ||||||
| chr3:119381359
|
A | G | 12 | a0001c0001t0029g0042a0001c0001t0045g0286a0001c0001t0052g0283others(9): Show | 12 | HG00639.hp1 HG00735.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.431+373A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381359 | ||||||
| chr3:119381369
|
T | C | 43 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0005g0278others(40): Show | 43 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.431+383T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381369 | ||||||
| chr3:119381398
|
A | G | 9 | a0001c0001t0029g0042a0001c0001t0045g0286a0001c0001t0052g0283others(6): Show | 9 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.431+412A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381398 | ||||||
| chr3:119381424
|
A | G | 3 | a0001c0001t0008g0192a0002c0003t0009g0167a0002c0003t0009g0194 | 3 | HG00280.hp2 HG02148.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.431+438A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381424 | ||||||
| chr3:119381456
|
T | A | 2 | a0001c0005t0001g0163a0001c0005t0001g0164 | 2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.431+470T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381456 | ||||||
| chr3:119381456
|
T | G | 11 | a0001c0001t0018g0208a0001c0001t0020g0010a0001c0001t0029g0042others(8): Show | 11 | HG00639.hp1 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.431+470T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381456 | ||||||
| chr3:119381711
|
T | A | 32 | a0001c0001t0008g0170a0001c0001t0008g0229a0001c0001t0008g0299others(29): Show | 32 | HG01071.hp2 HG01106.hp2 HG02015.hp2 others(29): Show |
intron_variant | MODIFIER | c.432-581T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381711 | ||||||
| chr3:119381718
|
T | C | 2 | a0001c0001t0006g0127a0001c0001t0053g0187 | 2 | HG01081.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.432-574T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381718 | ||||||
| chr3:119381725
|
T | C | 1 | a0001c0001t0005g0121 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.432-567T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381725 | ||||||
| chr3:119381754
|
C | G | 1 | a0001c0002t0001g0088 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.432-538C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381754 | ||||||
| chr3:119381762
|
C | T | 1 | a0001c0001t0020g0064 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.432-530C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381762 | ||||||
| chr3:119381769
|
G | A | 2 | a0001c0001t0006g0109a0001c0004t0003g0120 | 2 | HG02129.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.432-523G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381769 | ||||||
| chr3:119381779
|
G | A | 1 | a0001c0005t0001g0067 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.432-513G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381779 | ||||||
| chr3:119381792
|
A | C | 4 | a0001c0001t0007g0234a0001c0005t0001g0190a0003c0006t0022g0269others(1): Show | 4 | HG02055.hp2 NA18522.hp1 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.432-500A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381792 | ||||||
| chr3:119381852
|
G | A | 1 | a0002c0003t0009g0245 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.432-440G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381852 | ||||||
| chr3:119381885
|
A | C | 1 | a0001c0001t0017g0189 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.432-407A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381885 | ||||||
| chr3:119381917
|
C | T | 1 | a0003c0006t0001g0161 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.432-375C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381917 | ||||||
| chr3:119381918
|
G | A | 18 | a0001c0001t0025g0204a0001c0002t0001g0014a0001c0004t0003g0136others(15): Show | 18 | HG01243.hp2 HG01258.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.432-374G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381918 | ||||||
| chr3:119381952
|
C | G | 1 | a0001c0002t0004g0246 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.432-340C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381952 | ||||||
| chr3:119381965
|
G | C | 1 | a0002c0003t0002g0151 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.432-327G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381965 | ||||||
| chr3:119381983
|
C | A | 1 | a0001c0001t0008g0192 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.432-309C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381983 | ||||||
| chr3:119381985
|
C | CA | 19 | a0001c0001t0005g0153a0001c0001t0006g0131a0001c0001t0007g0228others(16): Show | 19 | HG01106.hp1 HG01361.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.432-284dupA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr3 | 119381985 | |||||
| chr3:119381985
|
CA | C | 91 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0142others(88): Show | 91 | HG00280.hp1 HG00597.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.432-284delA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr3 | 119381985 | |||||
| chr3:119381985
|
CAAAA | C | 19 | a0001c0001t0025g0204a0001c0002t0001g0014a0001c0004t0003g0136others(16): Show | 19 | HG00280.hp2 HG01243.hp2 HG01258.hp2 others(16): Show |
intron_variant | MODIFIER | c.432-287_432-284del others(4): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr3 | 119381985 | |||||
| chr3:119381994
|
A | G | 2 | a0001c0001t0005g0278a0001c0001t0040g0257 | 2 | HG02080.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.432-298A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381994 | ||||||
| chr3:119381995
|
A | G | 28 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0142others(25): Show | 28 | HG00597.hp2 HG01975.hp2 HG02056.hp2 others(25): Show |
intron_variant | MODIFIER | c.432-297A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119381995 | ||||||
| chr3:119382055
|
T | G | 8 | a0001c0001t0029g0042a0001c0001t0060g0026a0001c0002t0012g0174others(5): Show | 8 | HG01099.hp1 HG01106.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.432-237T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119382055 | ||||||
| chr3:119382192
|
T | A | 5 | a0001c0001t0025g0223a0001c0001t0042g0282a0002c0003t0002g0118others(2): Show | 5 | HG00280.hp1 HG00280.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.432-100T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 4/11 | chr3 | 119382192 | ||||||
| chr3:119382528
|
G | A | 3 | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0259 | 3 | NA18940.hp1 NA18955.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.539+129G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 5/11 | chr3 | 119382528 | ||||||
| chr3:119382584
|
A | T | 1 | a0001c0002t0001g0132 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.539+185A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 5/11 | chr3 | 119382584 | ||||||
| chr3:119382674
|
GCCTTTAT others(4): Show |
G | 1 | a0002c0003t0009g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.539+276_539+286del others(11): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 5/11 | chr3 | 119382674 | ||||||
| chr3:119382764
|
T | C | 1 | a0001c0005t0014g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.540-320T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 5/11 | chr3 | 119382764 | ||||||
| chr3:119382829
|
C | A | 1 | a0001c0001t0017g0302 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.540-255C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 5/11 | chr3 | 119382829 | ||||||
| chr3:119382914
|
G | A | 5 | a0001c0002t0004g0256a0001c0002t0012g0206a0001c0005t0023g0193others(2): Show | 5 | HG02257.hp2 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.540-170G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 5/11 | chr3 | 119382914 | ||||||
| chr3:119383038
|
T | TTG | 15 | a0001c0001t0005g0022a0001c0001t0005g0111a0001c0001t0007g0293others(12): Show | 16 | HG00639.hp2 HG00735.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.540-44_540-43dupGT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr3 | 119383038 | |||||
| chr3:119383078
|
C | T | 15 | a0001c0001t0005g0022a0001c0001t0005g0111a0001c0001t0007g0293others(12): Show | 16 | HG00639.hp2 HG00735.hp2 HG00741.hp1 others(13): Show |
splice_region_variant&intron_variant | LOW | c.540-6C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 5/11 | chr3 | 119383078 | ||||||
| chr3:119383245
|
A | C | 7 | a0001c0001t0040g0257a0001c0002t0001g0008a0001c0002t0001g0070others(4): Show | 7 | HG01884.hp1 HG02895.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.682+19A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119383245 | ||||||
| chr3:119383340
|
T | G | 5 | a0001c0002t0004g0256a0001c0002t0012g0206a0001c0005t0023g0193others(2): Show | 5 | HG02257.hp2 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+114T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119383340 | ||||||
| chr3:119383403
|
G | A | 79 | a0001c0001t0005g0117a0001c0001t0006g0065a0001c0001t0006g0066others(76): Show | 79 | HG00280.hp1 HG00280.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.682+177G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119383403 | ||||||
| chr3:119383427
|
T | C | 4 | a0001c0004t0021g0048a0001c0004t0021g0055a0001c0005t0014g0047others(1): Show | 4 | HG02258.hp2 HG02922.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+201T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119383427 | ||||||
| chr3:119383611
|
G | A | 156 | a0001c0001t0005g0022a0001c0001t0005g0087a0001c0001t0005g0111others(153): Show | 158 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.682+385G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119383611 | ||||||
| chr3:119383649
|
T | C | 31 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(28): Show | 31 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.682+423T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119383649 | ||||||
| chr3:119383969
|
T | C | 1 | a0001c0001t0011g0301 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.682+743T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119383969 | ||||||
| chr3:119384185
|
A | G | 9 | a0001c0001t0020g0010a0001c0001t0050g0177a0001c0005t0001g0160others(6): Show | 9 | HG00639.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.682+959A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119384185 | ||||||
| chr3:119384272
|
C | T | 3 | a0004c0007t0015g0016a0004c0007t0044g0196a0004c0007t0054g0205 | 3 | HG01884.hp1 HG02895.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.682+1046C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119384272 | ||||||
| chr3:119384321
|
T | A | 1 | a0001c0002t0016g0099 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.682+1095T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119384321 | ||||||
| chr3:119384434
|
G | T | 1 | a0003c0006t0056g0011 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.682+1208G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119384434 | ||||||
| chr3:119384733
|
G | T | 56 | a0001c0001t0005g0117a0001c0001t0006g0065a0001c0001t0006g0066others(53): Show | 56 | HG00597.hp1 HG00621.hp1 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.682+1507G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119384733 | ||||||
| chr3:119384793
|
G | A | 34 | a0001c0001t0020g0010a0001c0001t0025g0204a0001c0001t0025g0223others(31): Show | 34 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.682+1567G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119384793 | ||||||
| chr3:119384827
|
C | G | 139 | a0001c0001t0005g0117a0001c0001t0005g0121a0001c0001t0005g0129others(136): Show | 140 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.682+1601C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119384827 | ||||||
| chr3:119384834
|
C | G | 12 | a0001c0001t0020g0010a0001c0001t0050g0177a0001c0005t0001g0160others(9): Show | 12 | HG00639.hp1 HG01884.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.682+1608C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119384834 | ||||||
| chr3:119384928
|
C | CT | 22 | a0001c0001t0005g0022a0001c0001t0005g0111a0001c0001t0007g0293others(19): Show | 23 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.682+1717dupT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119384928 | |||||
| chr3:119384955
|
C | T | 2 | a0001c0001t0029g0042a0001c0001t0029g0054 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.682+1729C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119384955 | ||||||
| chr3:119384986
|
G | A | 1 | a0001c0002t0004g0247 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.682+1760G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119384986 | ||||||
| chr3:119385162
|
A | G | 81 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(78): Show | 82 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.682+1936A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119385162 | ||||||
| chr3:119385220
|
G | A | 1 | a0001c0001t0060g0026 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.682+1994G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119385220 | ||||||
| chr3:119385232
|
G | GT | 79 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(76): Show | 80 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.682+2016dupT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119385232 | |||||
| chr3:119385261
|
G | A | 19 | a0001c0002t0001g0014a0001c0004t0003g0007a0001c0004t0003g0038others(16): Show | 19 | HG00099.hp2 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.682+2035G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119385261 | ||||||
| chr3:119385414
|
A | G | 16 | a0001c0002t0004g0247a0001c0002t0012g0174a0001c0004t0021g0048others(13): Show | 16 | HG01099.hp1 HG01106.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.682+2188A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119385414 | ||||||
| chr3:119385463
|
G | A | 16 | a0001c0002t0004g0247a0001c0002t0012g0174a0001c0004t0021g0048others(13): Show | 16 | HG01099.hp1 HG01106.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.682+2237G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119385463 | ||||||
| chr3:119385501
|
C | T | 1 | a0001c0002t0012g0206 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.682+2275C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119385501 | ||||||
| chr3:119385778
|
G | A | 56 | a0001c0001t0005g0121a0001c0001t0005g0129a0001c0001t0006g0025others(53): Show | 57 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.682+2552G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119385778 | ||||||
| chr3:119385783
|
G | C | 16 | a0001c0002t0004g0247a0001c0002t0012g0174a0001c0004t0021g0048others(13): Show | 16 | HG01099.hp1 HG01106.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.682+2557G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119385783 | ||||||
| chr3:119385792
|
A | G | 1 | a0001c0005t0047g0239 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.682+2566A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119385792 | ||||||
| chr3:119386134
|
A | G | 22 | a0001c0001t0025g0204a0001c0001t0025g0223a0001c0001t0042g0282others(19): Show | 22 | HG00280.hp1 HG00280.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.682+2908A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119386134 | ||||||
| chr3:119386263
|
T | TA | 17 | a0001c0001t0005g0022a0001c0001t0005g0111a0001c0001t0006g0109others(14): Show | 18 | HG00639.hp2 HG00735.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.682+3045dupA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119386263 | |||||
| chr3:119386292
|
A | G | 1 | a0001c0002t0004g0247 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.682+3066A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119386292 | ||||||
| chr3:119386343
|
C | T | 31 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(28): Show | 31 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.682+3117C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119386343 | ||||||
| chr3:119386513
|
G | T | 2 | a0001c0002t0012g0174a0003c0006t0013g0031 | 2 | HG01099.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.682+3287G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119386513 | ||||||
| chr3:119386522
|
T | G | 5 | a0001c0002t0004g0256a0001c0002t0012g0206a0001c0005t0023g0193others(2): Show | 5 | HG02257.hp2 HG02647.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+3296T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119386522 | ||||||
| chr3:119386555
|
T | C | 22 | a0001c0001t0025g0204a0001c0001t0025g0223a0001c0001t0042g0282others(19): Show | 22 | HG00280.hp1 HG00280.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.682+3329T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119386555 | ||||||
| chr3:119386630
|
G | A | 16 | a0001c0002t0004g0247a0001c0002t0012g0174a0001c0004t0021g0048others(13): Show | 16 | HG01099.hp1 HG01106.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.682+3404G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119386630 | ||||||
| chr3:119386649
|
C | T | 1 | a0001c0001t0005g0142 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.682+3423C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119386649 | ||||||
| chr3:119386709
|
T | G | 16 | a0001c0002t0004g0247a0001c0002t0012g0174a0001c0004t0021g0048others(13): Show | 16 | HG01099.hp1 HG01106.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.682+3483T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119386709 | ||||||
| chr3:119386816
|
C | T | 58 | a0001c0001t0005g0117a0001c0001t0006g0065a0001c0001t0006g0066others(55): Show | 58 | HG00597.hp1 HG00621.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.682+3590C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119386816 | ||||||
| chr3:119386830
|
T | G | 1 | a0001c0004t0003g0120 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.682+3604T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119386830 | ||||||
| chr3:119387111
|
AC | A | 77 | a0001c0001t0005g0117a0001c0001t0006g0065a0001c0001t0006g0066others(74): Show | 77 | HG00597.hp1 HG00621.hp1 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.683-3668delC | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119387111 | |||||
| chr3:119387255
|
C | T | 16 | a0001c0002t0004g0247a0001c0002t0012g0174a0001c0004t0021g0048others(13): Show | 16 | HG01099.hp1 HG01106.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.683-3530C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119387255 | ||||||
| chr3:119387266
|
G | T | 9 | a0001c0001t0020g0010a0001c0001t0050g0177a0001c0005t0001g0160others(6): Show | 9 | HG00639.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.683-3519G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119387266 | ||||||
| chr3:119387567
|
A | G | 1 | a0001c0004t0010g0002 | 2 | NA18944.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.683-3218A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119387567 | ||||||
| chr3:119387803
|
G | A | 9 | a0001c0002t0001g0014a0001c0005t0001g0012a0001c0005t0001g0019others(6): Show | 9 | HG01243.hp2 HG02486.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.683-2982G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119387803 | ||||||
| chr3:119387870
|
A | G | 1 | a0001c0004t0003g0110 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.683-2915A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119387870 | ||||||
| chr3:119387888
|
G | A | 2 | a0001c0001t0020g0010a0001c0001t0050g0177 | 2 | HG02683.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.683-2897G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119387888 | ||||||
| chr3:119387907
|
G | A | 2 | a0001c0001t0029g0042a0001c0001t0029g0054 | 2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.683-2878G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119387907 | ||||||
| chr3:119388085
|
A | G | 21 | a0001c0002t0004g0247a0001c0002t0004g0256a0001c0002t0012g0174others(18): Show | 21 | HG01099.hp1 HG01106.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.683-2700A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119388085 | ||||||
| chr3:119388090
|
G | T | 1 | a0001c0002t0004g0242 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.683-2695G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119388090 | ||||||
| chr3:119388136
|
G | A | 1 | a0004c0007t0015g0162 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.683-2649G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119388136 | ||||||
| chr3:119388179
|
T | C | 1 | a0001c0001t0042g0282 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.683-2606T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119388179 | ||||||
| chr3:119388231
|
T | TTA | 21 | a0001c0002t0004g0247a0001c0002t0004g0256a0001c0002t0012g0174others(18): Show | 21 | HG01099.hp1 HG01106.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.683-2553_683-2552i others(4): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119388231 | |||||
| chr3:119388306
|
T | TTACATA | 21 | a0001c0001t0005g0022a0001c0001t0005g0111a0001c0001t0007g0293others(18): Show | 22 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.683-2478_683-2477i others(8): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119388306 | |||||
| chr3:119388306
|
T | TTACATAT others(3): Show |
32 | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0005g0142others(29): Show | 32 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.683-2478_683-2477i others(12): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119388306 | |||||
| chr3:119388306
|
T | TTACATAT others(5): Show |
11 | a0001c0001t0005g0058a0001c0001t0007g0250a0001c0001t0007g0272others(8): Show | 11 | HG02055.hp1 HG02280.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.683-2478_683-2477i others(14): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119388306 | |||||
| chr3:119388306
|
T | TTACATAT others(7): Show |
18 | a0001c0001t0008g0192a0001c0001t0039g0260a0001c0001t0040g0257others(15): Show | 18 | HG01071.hp2 HG01884.hp2 HG02148.hp1 others(15): Show |
intron_variant | MODIFIER | c.683-2478_683-2477i others(16): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119388306 | |||||
| chr3:119388306
|
T | TTACATAT others(9): Show |
26 | a0001c0001t0005g0117a0001c0001t0006g0065a0001c0001t0006g0066others(23): Show | 26 | HG00738.hp2 HG01106.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.683-2478_683-2477i others(18): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119388306 | |||||
| chr3:119388306
|
T | TTACATAT others(11): Show |
12 | a0001c0001t0006g0025a0001c0001t0008g0178a0001c0001t0008g0273others(9): Show | 12 | HG02717.hp2 HG03195.hp2 HG03927.hp2 others(9): Show |
intron_variant | MODIFIER | c.683-2478_683-2477i others(20): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119388306 | |||||
| chr3:119388306
|
T | TTACATAT others(13): Show |
38 | a0001c0001t0005g0129a0001c0001t0006g0094a0001c0001t0006g0103others(35): Show | 39 | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.683-2478_683-2477i others(22): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119388306 | |||||
| chr3:119388306
|
T | TTACATAT others(15): Show |
11 | a0001c0001t0008g0200a0001c0001t0018g0209a0001c0001t0020g0043others(8): Show | 11 | HG00597.hp1 HG01081.hp1 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.683-2478_683-2477i others(24): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119388306 | |||||
| chr3:119388306
|
T | TTACATAT others(17): Show |
8 | a0001c0001t0006g0092a0001c0001t0006g0124a0001c0001t0008g0199others(5): Show | 8 | HG00639.hp1 HG02135.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.683-2478_683-2477i others(26): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119388306 | |||||
| chr3:119388306
|
T | TTACATAT others(19): Show |
6 | a0001c0001t0005g0121a0001c0001t0006g0102a0001c0001t0006g0109others(3): Show | 6 | HG01243.hp1 HG02129.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-2478_683-2477i others(28): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119388306 | |||||
| chr3:119388306
|
T | TTACATAT others(21): Show |
3 | a0001c0001t0020g0056a0001c0001t0024g0221a0001c0002t0001g0171 | 3 | HG00408.hp1 HG03130.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.683-2478_683-2477i others(30): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119388306 | |||||
| chr3:119388306
|
T | TTACATAT others(23): Show |
7 | a0001c0001t0008g0170a0001c0001t0018g0208a0001c0001t0020g0064others(4): Show | 7 | HG03239.hp2 HG04228.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.683-2478_683-2477i others(32): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119388306 | |||||
| chr3:119388306
|
TTTTA | T | 7 | a0001c0004t0003g0007a0001c0004t0003g0150a0001c0004t0010g0195others(4): Show | 7 | HG00099.hp2 HG01167.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-2477_683-2474d others(6): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119388306 | |||||
| chr3:119388306
|
TTTTATA | T | 4 | a0001c0004t0059g0015a0001c0005t0001g0067a0001c0005t0001g0069others(1): Show | 4 | HG01099.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-2477_683-2472d others(8): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119388306 | |||||
| chr3:119388308
|
T | A | 253 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(250): Show | 255 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.683-2477T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119388308 | ||||||
| chr3:119388315
|
T | C | 4 | a0001c0004t0059g0015a0001c0005t0001g0067a0001c0005t0001g0069others(1): Show | 4 | HG01099.hp2 HG02145.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-2470T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119388315 | ||||||
| chr3:119388405
|
T | G | 261 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(258): Show | 263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.683-2380T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119388405 | ||||||
| chr3:119388430
|
C | T | 58 | a0001c0001t0005g0117a0001c0001t0006g0065a0001c0001t0006g0066others(55): Show | 58 | HG00597.hp1 HG00621.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.683-2355C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119388430 | ||||||
| chr3:119388538
|
C | T | 2 | a0001c0001t0007g0226a0001c0001t0007g0227 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.683-2247C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119388538 | ||||||
| chr3:119388663
|
G | A | 6 | a0001c0001t0025g0204a0001c0001t0025g0223a0001c0001t0042g0282others(3): Show | 6 | HG00280.hp1 HG00280.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-2122G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119388663 | ||||||
| chr3:119388749
|
G | A | 1 | a0001c0005t0014g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.683-2036G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119388749 | ||||||
| chr3:119388763
|
C | T | 32 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(29): Show | 32 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.683-2022C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119388763 | ||||||
| chr3:119388927
|
C | T | 57 | a0001c0001t0006g0065a0001c0001t0006g0066a0001c0001t0006g0109others(54): Show | 57 | HG00597.hp1 HG00621.hp1 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.683-1858C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119388927 | ||||||
| chr3:119388931
|
C | T | 16 | a0001c0002t0004g0247a0001c0002t0012g0174a0001c0004t0021g0048others(13): Show | 16 | HG01099.hp1 HG01106.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.683-1854C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119388931 | ||||||
| chr3:119389022
|
A | G | 21 | a0001c0002t0004g0247a0001c0002t0004g0256a0001c0002t0012g0174others(18): Show | 21 | HG01099.hp1 HG01106.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.683-1763A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119389022 | ||||||
| chr3:119389098
|
T | C | 1 | a0012c0015t0035g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.683-1687T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119389098 | ||||||
| chr3:119389156
|
G | A | 3 | a0001c0001t0020g0010a0001c0001t0050g0177a0002c0003t0002g0060 | 3 | HG02683.hp2 HG02970.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.683-1629G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119389156 | ||||||
| chr3:119389219
|
A | G | 5 | a0001c0001t0018g0207a0001c0001t0018g0208a0001c0001t0018g0209others(2): Show | 5 | HG02683.hp1 HG03490.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-1566A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119389219 | ||||||
| chr3:119389278
|
A | G | 1 | a0001c0002t0001g0135 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.683-1507A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119389278 | ||||||
| chr3:119389752
|
T | C | 1 | a0001c0005t0014g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.683-1033T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119389752 | ||||||
| chr3:119389763
|
T | G | 2 | a0001c0001t0020g0010a0001c0001t0050g0177 | 2 | HG02683.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.683-1022T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119389763 | ||||||
| chr3:119389982
|
G | A | 2 | a0001c0001t0020g0010a0001c0001t0050g0177 | 2 | HG02683.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.683-803G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119389982 | ||||||
| chr3:119390024
|
C | T | 2 | a0003c0006t0013g0041a0003c0006t0013g0045 | 2 | HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.683-761C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119390024 | ||||||
| chr3:119390114
|
G | C | 1 | a0001c0002t0004g0247 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.683-671G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119390114 | ||||||
| chr3:119390124
|
G | A | 1 | a0001c0002t0004g0247 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.683-661G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119390124 | ||||||
| chr3:119390149
|
TA | T | 33 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(30): Show | 33 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.683-625delA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | 119390149 | |||||
| chr3:119390263
|
G | A | 1 | a0001c0001t0055g0306 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.683-522G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119390263 | ||||||
| chr3:119390291
|
A | G | 1 | a0001c0004t0010g0195 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.683-494A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119390291 | ||||||
| chr3:119390456
|
CATT | C | 61 | a0001c0001t0005g0121a0001c0001t0005g0129a0001c0001t0006g0025others(58): Show | 62 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.683-328_683-326del others(3): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119390456 | ||||||
| chr3:119390510
|
T | C | 1 | a0001c0005t0001g0191 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.683-275T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119390510 | ||||||
| chr3:119390643
|
G | A | 1 | a0002c0003t0009g0220 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.683-142G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | 119390643 | ||||||
| chr3:119390990
|
G | A | 14 | a0001c0001t0005g0087a0001c0001t0007g0275a0001c0001t0007g0296others(11): Show | 14 | HG00438.hp1 HG00735.hp1 HG00738.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.881+7G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119390990 | ||||||
| chr3:119391159
|
C | T | 37 | a0001c0001t0005g0058a0001c0001t0005g0121a0001c0001t0005g0129others(34): Show | 38 | HG00408.hp1 HG00408.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.881+176C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119391159 | ||||||
| chr3:119391425
|
G | A | 1 | a0002c0003t0009g0268 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.881+442G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119391425 | ||||||
| chr3:119391525
|
A | T | 1 | a0002c0003t0002g0032 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.881+542A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119391525 | ||||||
| chr3:119391589
|
AC | A | 66 | a0001c0001t0005g0087a0001c0001t0007g0275a0001c0001t0007g0296others(63): Show | 66 | HG00438.hp1 HG00621.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.881+614delC | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 119391589 | |||||
| chr3:119391595
|
C | T | 2 | a0001c0002t0004g0256a0001c0002t0012g0206 | 2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.881+612C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119391595 | ||||||
| chr3:119391597
|
C | T | 9 | a0001c0004t0003g0072a0002c0003t0002g0152a0002c0003t0030g0053others(6): Show | 9 | HG00735.hp2 HG00741.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.881+614C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119391597 | ||||||
| chr3:119391598
|
T | C | 31 | a0001c0001t0005g0117a0001c0001t0006g0066a0001c0001t0006g0094others(28): Show | 31 | HG00438.hp2 HG00597.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.881+615T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119391598 | ||||||
| chr3:119391598
|
T | TC | 49 | a0001c0001t0005g0096a0001c0001t0006g0025a0001c0001t0006g0092others(46): Show | 49 | HG00280.hp2 HG00408.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.881+622dupC | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 119391598 | |||||
| chr3:119391599
|
C | T | 1 | a0001c0001t0005g0117 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.881+616C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119391599 | ||||||
| chr3:119391604
|
C | G | 47 | a0001c0001t0005g0022a0001c0001t0005g0111a0001c0001t0007g0293others(44): Show | 49 | HG00099.hp2 HG00639.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.881+621C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119391604 | ||||||
| chr3:119391605
|
CG | C | 51 | a0001c0001t0005g0058a0001c0001t0005g0077a0001c0001t0005g0078others(48): Show | 51 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.881+623delG | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119391605 | ||||||
| chr3:119391606
|
G | C | 214 | a0001c0001t0005g0022a0001c0001t0005g0087a0001c0001t0005g0096others(211): Show | 216 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.881+623G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119391606 | ||||||
| chr3:119391606
|
G | T | 1 | a0001c0001t0020g0010 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.881+623G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119391606 | ||||||
| chr3:119391608
|
C | T | 1 | a0001c0004t0021g0059 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.881+625C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119391608 | ||||||
| chr3:119391613
|
C | T | 1 | a0010c0016t0004g0166 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.881+630C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119391613 | ||||||
| chr3:119391670
|
G | C | 2 | a0001c0004t0003g0120a0001c0004t0010g0244 | 2 | HG02129.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.881+687G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119391670 | ||||||
| chr3:119391745
|
G | C | 1 | a0011c0019t0005g0155 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.881+762G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119391745 | ||||||
| chr3:119391853
|
A | C | 37 | a0001c0001t0006g0025a0001c0001t0006g0065a0001c0001t0006g0066others(34): Show | 37 | HG00408.hp2 HG01071.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.881+870A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119391853 | ||||||
| chr3:119392021
|
C | T | 1 | a0012c0015t0035g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.881+1038C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119392021 | ||||||
| chr3:119392030
|
G | A | 1 | a0001c0005t0014g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.881+1047G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119392030 | ||||||
| chr3:119392110
|
G | A | 262 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(259): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.881+1127G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119392110 | ||||||
| chr3:119392202
|
C | T | 53 | a0001c0001t0025g0204a0001c0001t0025g0223a0001c0001t0029g0042others(50): Show | 54 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.881+1219C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119392202 | ||||||
| chr3:119392228
|
G | A | 39 | a0001c0004t0003g0007a0001c0004t0003g0021a0001c0004t0003g0024others(36): Show | 40 | HG00099.hp2 HG00741.hp2 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.882-1239G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119392228 | ||||||
| chr3:119392250
|
C | A | 1 | a0009c0017t0019g0185 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.882-1217C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119392250 | ||||||
| chr3:119392446
|
T | TCAA | 3 | a0001c0001t0006g0065a0001c0001t0006g0066a0002c0003t0002g0145 | 3 | HG01106.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.882-999_882-997dup others(3): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 119392446 | |||||
| chr3:119392627
|
G | A | 1 | a0001c0004t0003g0110 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.882-840G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119392627 | ||||||
| chr3:119392686
|
C | T | 2 | a0001c0004t0021g0059a0012c0015t0035g0237 | 2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.882-781C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119392686 | ||||||
| chr3:119392808
|
C | G | 1 | a0001c0002t0001g0088 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.882-659C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119392808 | ||||||
| chr3:119392915
|
T | C | 122 | a0001c0001t0005g0087a0001c0001t0005g0129a0001c0001t0006g0109others(119): Show | 122 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.882-552T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119392915 | ||||||
| chr3:119392936
|
G | A | 39 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(36): Show | 40 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.882-531G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119392936 | ||||||
| chr3:119392961
|
A | G | 48 | a0001c0001t0006g0025a0001c0001t0006g0065a0001c0001t0006g0066others(45): Show | 48 | HG00408.hp2 HG01071.hp1 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.882-506A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119392961 | ||||||
| chr3:119393023
|
T | C | 75 | a0001c0001t0005g0129a0001c0001t0006g0109a0001c0001t0007g0228others(72): Show | 75 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.882-444T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119393023 | ||||||
| chr3:119393229
|
C | G | 11 | a0001c0002t0004g0247a0001c0002t0012g0174a0003c0006t0001g0159others(8): Show | 11 | HG01099.hp1 HG01106.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.882-238C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119393229 | ||||||
| chr3:119393311
|
T | A | 1 | a0002c0003t0009g0248 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.882-156T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119393311 | ||||||
| chr3:119393316
|
ATCAAGCT | A | 4 | a0001c0001t0020g0010a0004c0007t0015g0016a0004c0007t0044g0196others(1): Show | 4 | HG01884.hp1 HG02895.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.882-149_882-143del others(7): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr3 | 119393316 | |||||
| chr3:119393328
|
T | G | 1 | a0001c0004t0051g0157 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.882-139T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 7/11 | chr3 | 119393328 | ||||||
| chr3:119393710
|
C | G | 3 | a0002c0003t0002g0082a0002c0003t0009g0245a0002c0003t0043g0210 | 3 | HG00621.hp2 HG02015.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1006+119C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119393710 | ||||||
| chr3:119393712
|
A | G | 210 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(207): Show | 211 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.1006+121A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119393712 | ||||||
| chr3:119393955
|
G | C | 10 | a0001c0002t0012g0174a0003c0006t0001g0159a0003c0006t0001g0161others(7): Show | 10 | HG01099.hp1 HG01106.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1006+364G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119393955 | ||||||
| chr3:119394051
|
G | A | 135 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(132): Show | 136 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1006+460G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119394051 | ||||||
| chr3:119394171
|
T | C | 55 | a0001c0001t0005g0087a0001c0001t0007g0275a0001c0001t0007g0296others(52): Show | 55 | HG00438.hp1 HG00621.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1006+580T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119394171 | ||||||
| chr3:119394384
|
G | T | 1 | a0001c0001t0042g0282 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1006+793G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119394384 | ||||||
| chr3:119394490
|
T | G | 210 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(207): Show | 211 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.1006+899T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119394490 | ||||||
| chr3:119394497
|
G | A | 7 | a0001c0001t0025g0204a0001c0001t0025g0223a0001c0001t0042g0282others(4): Show | 7 | HG00280.hp1 HG00280.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1006+906G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119394497 | ||||||
| chr3:119394650
|
C | A | 13 | a0001c0001t0005g0117a0001c0001t0018g0207a0001c0001t0018g0208others(10): Show | 13 | HG02055.hp1 HG02572.hp2 HG02683.hp1 others(10): Show |
intron_variant | MODIFIER | c.1006+1059C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119394650 | ||||||
| chr3:119394670
|
G | A | 8 | a0001c0001t0018g0207a0001c0001t0018g0208a0001c0001t0018g0209others(5): Show | 8 | HG02683.hp1 HG03130.hp2 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.1006+1079G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119394670 | ||||||
| chr3:119394690
|
C | T | 1 | a0001c0005t0049g0289 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1006+1099C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119394690 | ||||||
| chr3:119394823
|
A | C | 1 | a0001c0002t0001g0135 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1006+1232A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119394823 | ||||||
| chr3:119394883
|
T | G | 1 | a0001c0005t0014g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1006+1292T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119394883 | ||||||
| chr3:119394912
|
T | G | 4 | a0001c0001t0061g0057a0001c0004t0021g0048a0001c0004t0021g0055others(1): Show | 4 | HG02258.hp2 HG02486.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1006+1321T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119394912 | ||||||
| chr3:119394915
|
G | A | 39 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(36): Show | 40 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.1006+1324G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119394915 | ||||||
| chr3:119394923
|
A | G | 1 | a0010c0016t0004g0166 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1006+1332A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119394923 | ||||||
| chr3:119394973
|
A | C | 137 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(134): Show | 139 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1006+1382A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119394973 | ||||||
| chr3:119395116
|
T | C | 1 | a0001c0004t0003g0113 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1006+1525T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119395116 | ||||||
| chr3:119395384
|
G | C | 47 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(44): Show | 48 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1006+1793G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119395384 | ||||||
| chr3:119395555
|
A | G | 1 | a0001c0001t0007g0296 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1006+1964A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119395555 | ||||||
| chr3:119395668
|
G | A | 131 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(128): Show | 133 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1006+2077G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119395668 | ||||||
| chr3:119395846
|
A | G | 196 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(193): Show | 198 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.1006+2255A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119395846 | ||||||
| chr3:119395919
|
A | G | 1 | a0001c0001t0006g0148 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1006+2328A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119395919 | ||||||
| chr3:119395945
|
G | A | 2 | a0002c0003t0002g0118a0002c0003t0009g0167 | 2 | HG00280.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1006+2354G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119395945 | ||||||
| chr3:119395993
|
G | A | 9 | a0001c0001t0018g0207a0001c0001t0018g0208a0001c0001t0018g0209others(6): Show | 9 | HG02683.hp1 HG02970.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.1006+2402G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119395993 | ||||||
| chr3:119396080
|
T | C | 186 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(183): Show | 188 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1006+2489T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119396080 | ||||||
| chr3:119396092
|
A | G | 9 | a0001c0001t0018g0207a0001c0001t0018g0208a0001c0001t0018g0209others(6): Show | 9 | HG02683.hp1 HG02970.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.1006+2501A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119396092 | ||||||
| chr3:119396336
|
T | C | 1 | a0004c0007t0015g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1006+2745T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119396336 | ||||||
| chr3:119396396
|
C | T | 13 | a0001c0004t0059g0015a0003c0006t0001g0159a0003c0006t0001g0161others(10): Show | 13 | HG01099.hp1 HG01099.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.1007-2803C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119396396 | ||||||
| chr3:119396685
|
A | G | 92 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(89): Show | 93 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1007-2514A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119396685 | ||||||
| chr3:119396709
|
T | C | 190 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(187): Show | 192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.1007-2490T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119396709 | ||||||
| chr3:119396720
|
A | G | 190 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(187): Show | 192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.1007-2479A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119396720 | ||||||
| chr3:119396883
|
T | C | 1 | a0001c0002t0004g0247 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1007-2316T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119396883 | ||||||
| chr3:119397035
|
G | A | 4 | a0001c0002t0001g0108a0001c0002t0001g0135a0001c0002t0001g0173others(1): Show | 4 | NA18950.hp1 NA19067.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-2164G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119397035 | ||||||
| chr3:119397128
|
A | T | 37 | a0001c0004t0003g0007a0001c0004t0003g0021a0001c0004t0003g0024others(34): Show | 38 | HG00099.hp2 HG00741.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1007-2071A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119397128 | ||||||
| chr3:119397217
|
A | C | 197 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(194): Show | 199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1007-1982A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119397217 | ||||||
| chr3:119397250
|
C | T | 7 | a0004c0007t0015g0016a0004c0007t0015g0030a0004c0007t0015g0052others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1007-1949C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119397250 | ||||||
| chr3:119397303
|
G | A | 54 | a0001c0001t0005g0129a0001c0001t0007g0228a0001c0001t0007g0254others(51): Show | 54 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.1007-1896G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119397303 | ||||||
| chr3:119397335
|
C | T | 7 | a0004c0007t0015g0016a0004c0007t0015g0030a0004c0007t0015g0052others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1007-1864C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119397335 | ||||||
| chr3:119397339
|
C | T | 1 | a0002c0003t0002g0151 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1007-1860C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119397339 | ||||||
| chr3:119397360
|
C | T | 1 | a0001c0001t0011g0186 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1007-1839C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119397360 | ||||||
| chr3:119397621
|
C | T | 7 | a0004c0007t0015g0016a0004c0007t0015g0030a0004c0007t0015g0052others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1007-1578C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119397621 | ||||||
| chr3:119397761
|
G | A | 13 | a0001c0004t0059g0015a0003c0006t0001g0159a0003c0006t0001g0161others(10): Show | 13 | HG01099.hp1 HG01099.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.1007-1438G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119397761 | ||||||
| chr3:119397889
|
T | C | 4 | a0001c0004t0021g0048a0001c0004t0021g0055a0001c0004t0021g0059others(1): Show | 4 | HG02055.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007-1310T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119397889 | ||||||
| chr3:119397991
|
T | A | 1 | a0002c0018t0019g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1007-1208T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119397991 | ||||||
| chr3:119398051
|
G | A | 1 | a0001c0001t0005g0142 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1007-1148G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119398051 | ||||||
| chr3:119398084
|
C | T | 191 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(188): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1007-1115C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119398084 | ||||||
| chr3:119398198
|
T | C | 7 | a0004c0007t0015g0016a0004c0007t0015g0030a0004c0007t0015g0052others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1007-1001T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119398198 | ||||||
| chr3:119398542
|
A | G | 57 | a0001c0004t0003g0007a0001c0004t0003g0021a0001c0004t0003g0024others(54): Show | 58 | HG00099.hp2 HG00741.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.1007-657A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119398542 | ||||||
| chr3:119398755
|
T | C | 1 | a0001c0001t0005g0278 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1007-444T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119398755 | ||||||
| chr3:119398857
|
T | C | 1 | a0001c0001t0024g0221 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1007-342T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119398857 | ||||||
| chr3:119398989
|
T | C | 4 | a0001c0004t0021g0048a0001c0004t0021g0055a0001c0004t0021g0059others(1): Show | 4 | HG02055.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1007-210T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119398989 | ||||||
| chr3:119399087
|
G | A | 4 | a0001c0001t0025g0204a0001c0001t0025g0223a0001c0001t0042g0282others(1): Show | 4 | HG00280.hp1 HG01361.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-112G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 8/11 | chr3 | 119399087 | ||||||
| chr3:119399367
|
C | T | 1 | a0001c0004t0038g0181 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1069+106C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119399367 | ||||||
| chr3:119399390
|
C | T | 3 | a0001c0001t0007g0241a0001c0001t0007g0276a0001c0001t0011g0183 | 3 | HG02602.hp1 HG02698.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1069+129C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119399390 | ||||||
| chr3:119399431
|
A | G | 1 | a0001c0001t0024g0243 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1069+170A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119399431 | ||||||
| chr3:119399527
|
A | T | 3 | a0001c0001t0029g0042a0001c0001t0029g0054a0001c0001t0040g0257 | 3 | HG02896.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1069+266A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119399527 | ||||||
| chr3:119399597
|
A | G | 9 | a0001c0001t0018g0207a0001c0001t0018g0208a0001c0001t0018g0209others(6): Show | 9 | HG02683.hp1 HG02970.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.1069+336A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119399597 | ||||||
| chr3:119399614
|
T | A | 83 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(80): Show | 84 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1069+353T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119399614 | ||||||
| chr3:119399650
|
A | G | 92 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(89): Show | 93 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1069+389A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119399650 | ||||||
| chr3:119399724
|
T | C | 2 | a0001c0001t0008g0215a0001c0001t0008g0216 | 2 | HG01255.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1069+463T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119399724 | ||||||
| chr3:119399949
|
T | G | 83 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(80): Show | 84 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1069+688T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119399949 | ||||||
| chr3:119400013
|
T | A | 5 | a0001c0001t0025g0204a0001c0001t0025g0223a0001c0001t0042g0282others(2): Show | 5 | HG00280.hp1 HG01081.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1069+752T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400013 | ||||||
| chr3:119400098
|
A | C | 57 | a0001c0004t0003g0007a0001c0004t0003g0021a0001c0004t0003g0024others(54): Show | 58 | HG00099.hp2 HG00741.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.1069+837A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400098 | ||||||
| chr3:119400311
|
C | T | 37 | a0001c0004t0003g0007a0001c0004t0003g0021a0001c0004t0003g0024others(34): Show | 38 | HG00099.hp2 HG00741.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1069+1050C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400311 | ||||||
| chr3:119400389
|
G | A | 7 | a0004c0007t0015g0016a0004c0007t0015g0030a0004c0007t0015g0052others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1069+1128G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400389 | ||||||
| chr3:119400414
|
C | G | 1 | a0001c0002t0018g0305 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1069+1153C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400414 | ||||||
| chr3:119400431
|
G | A | 41 | a0001c0005t0001g0005a0001c0005t0001g0012a0001c0005t0001g0019others(38): Show | 41 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1069+1170G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400431 | ||||||
| chr3:119400464
|
T | A | 51 | a0001c0004t0003g0007a0001c0004t0003g0021a0001c0004t0003g0024others(48): Show | 52 | HG00099.hp2 HG00741.hp2 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.1069+1203T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400464 | ||||||
| chr3:119400467
|
T | A | 1 | a0003c0006t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1069+1206T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400467 | ||||||
| chr3:119400489
|
C | T | 298 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(295): Show | 300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1069+1228C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400489 | ||||||
| chr3:119400525
|
T | A | 8 | a0001c0001t0005g0022a0001c0001t0005g0111a0001c0001t0007g0293others(5): Show | 9 | HG00639.hp2 HG01081.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1069+1264T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400525 | ||||||
| chr3:119400548
|
T | C | 1 | a0001c0001t0017g0189 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1070-1274T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400548 | ||||||
| chr3:119400586
|
A | C | 257 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1070-1236A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400586 | ||||||
| chr3:119400676
|
G | A | 41 | a0001c0005t0001g0005a0001c0005t0001g0012a0001c0005t0001g0019others(38): Show | 41 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1070-1146G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400676 | ||||||
| chr3:119400689
|
G | A | 92 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(89): Show | 93 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1070-1133G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400689 | ||||||
| chr3:119400706
|
T | C | 57 | a0001c0004t0003g0007a0001c0004t0003g0021a0001c0004t0003g0024others(54): Show | 58 | HG00099.hp2 HG00741.hp2 HG01099.hp1 others(55): Show |
intron_variant | MODIFIER | c.1070-1116T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400706 | ||||||
| chr3:119400738
|
A | C | 1 | a0001c0001t0005g0278 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1070-1084A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400738 | ||||||
| chr3:119400892
|
T | C | 257 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(254): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1070-930T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400892 | ||||||
| chr3:119400928
|
T | C | 1 | a0001c0002t0004g0242 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1070-894T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400928 | ||||||
| chr3:119400932
|
A | G | 1 | a0001c0002t0004g0242 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1070-890A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400932 | ||||||
| chr3:119400937
|
G | A | 1 | a0003c0006t0013g0045 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1070-885G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119400937 | ||||||
| chr3:119401014
|
T | C | 7 | a0001c0002t0001g0008a0001c0002t0001g0014a0001c0002t0001g0070others(4): Show | 7 | HG02257.hp2 HG02723.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1070-808T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119401014 | ||||||
| chr3:119401032
|
G | A | 5 | a0001c0001t0025g0204a0001c0001t0025g0223a0001c0001t0042g0282others(2): Show | 5 | HG00280.hp1 HG01081.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1070-790G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119401032 | ||||||
| chr3:119401098
|
G | A | 1 | a0001c0001t0007g0276 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1070-724G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119401098 | ||||||
| chr3:119401145
|
T | A | 7 | a0004c0007t0015g0016a0004c0007t0015g0030a0004c0007t0015g0052others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1070-677T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119401145 | ||||||
| chr3:119401148
|
G | C | 7 | a0004c0007t0015g0016a0004c0007t0015g0030a0004c0007t0015g0052others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1070-674G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119401148 | ||||||
| chr3:119401157
|
C | G | 7 | a0004c0007t0015g0016a0004c0007t0015g0030a0004c0007t0015g0052others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1070-665C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119401157 | ||||||
| chr3:119401158
|
T | G | 7 | a0004c0007t0015g0016a0004c0007t0015g0030a0004c0007t0015g0052others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1070-664T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119401158 | ||||||
| chr3:119401159
|
G | A | 7 | a0004c0007t0015g0016a0004c0007t0015g0030a0004c0007t0015g0052others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1070-663G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119401159 | ||||||
| chr3:119401160
|
T | G | 7 | a0004c0007t0015g0016a0004c0007t0015g0030a0004c0007t0015g0052others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1070-662T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119401160 | ||||||
| chr3:119401166
|
A | G | 7 | a0004c0007t0015g0016a0004c0007t0015g0030a0004c0007t0015g0052others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1070-656A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119401166 | ||||||
| chr3:119401170
|
C | CA | 156 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(153): Show | 158 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.1070-635dupA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr3 | 119401170 | |||||
| chr3:119401170
|
CA | C | 9 | a0001c0001t0039g0260a0001c0001t0045g0286a0001c0001t0052g0283others(6): Show | 9 | HG01106.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1070-635delA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr3 | 119401170 | |||||
| chr3:119401194
|
C | T | 9 | a0001c0005t0001g0005a0001c0005t0001g0049a0001c0005t0014g0009others(6): Show | 9 | HG00735.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1070-628C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119401194 | ||||||
| chr3:119401212
|
TAACAGTT others(5): Show |
T | 1 | a0001c0001t0007g0250 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1070-608_1070-597d others(14): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr3 | 119401212 | |||||
| chr3:119401263
|
A | T | 3 | a0001c0001t0029g0042a0001c0001t0029g0054a0001c0001t0040g0257 | 3 | HG02896.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1070-559A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119401263 | ||||||
| chr3:119401397
|
G | A | 1 | a0003c0006t0001g0161 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1070-425G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119401397 | ||||||
| chr3:119401535
|
G | A | 43 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(40): Show | 44 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.1070-287G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119401535 | ||||||
| chr3:119401682
|
G | T | 1 | a0001c0002t0004g0242 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1070-140G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119401682 | ||||||
| chr3:119401730
|
G | C | 92 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(89): Show | 93 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1070-92G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 9/11 | chr3 | 119401730 | ||||||
| chr3:119402563
|
G | A | 1 | a0001c0004t0059g0015 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1645+166G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119402563 | ||||||
| chr3:119402823
|
C | T | 1 | a0002c0003t0009g0201 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1645+426C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119402823 | ||||||
| chr3:119402832
|
T | C | 5 | a0001c0001t0025g0204a0001c0001t0025g0223a0001c0001t0042g0282others(2): Show | 5 | HG00280.hp1 HG01081.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1645+435T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119402832 | ||||||
| chr3:119402963
|
T | A | 42 | a0001c0005t0001g0005a0001c0005t0001g0012a0001c0005t0001g0019others(39): Show | 42 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1645+566T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119402963 | ||||||
| chr3:119403155
|
C | T | 2 | a0001c0005t0001g0034a0001c0005t0001g0046 | 2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1645+758C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119403155 | ||||||
| chr3:119403176
|
G | C | 3 | a0001c0002t0003g0143a0001c0002t0003g0144a0001c0002t0004g0262 | 3 | NA18955.hp2 NA18995.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1645+779G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119403176 | ||||||
| chr3:119403191
|
G | A | 22 | a0001c0001t0018g0207a0001c0001t0018g0208a0001c0001t0018g0209others(19): Show | 22 | HG01099.hp1 HG01099.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1645+794G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119403191 | ||||||
| chr3:119403195
|
A | C | 2 | a0001c0001t0046g0307a0001c0001t0055g0306 | 2 | NA19060.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1645+798A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119403195 | ||||||
| chr3:119403213
|
A | C | 3 | a0001c0001t0039g0260a0001c0001t0045g0286a0001c0001t0052g0283 | 3 | HG02615.hp1 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1645+816A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119403213 | ||||||
| chr3:119403409
|
C | T | 1 | a0001c0001t0060g0026 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1645+1012C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119403409 | ||||||
| chr3:119403587
|
A | G | 1 | a0001c0001t0011g0158 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1645+1190A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119403587 | ||||||
| chr3:119403619
|
T | A | 3 | a0001c0001t0025g0204a0001c0001t0025g0223a0001c0001t0042g0282 | 3 | HG00280.hp1 HG01934.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.1645+1222T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119403619 | ||||||
| chr3:119403686
|
G | A | 2 | a0001c0001t0007g0226a0001c0001t0007g0227 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1645+1289G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119403686 | ||||||
| chr3:119403838
|
T | A | 1 | a0003c0006t0013g0041 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1645+1441T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119403838 | ||||||
| chr3:119403921
|
G | A | 1 | a0003c0006t0001g0161 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1645+1524G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119403921 | ||||||
| chr3:119403949
|
G | T | 41 | a0001c0005t0001g0005a0001c0005t0001g0012a0001c0005t0001g0019others(38): Show | 41 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1645+1552G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119403949 | ||||||
| chr3:119403973
|
T | C | 54 | a0001c0001t0005g0129a0001c0001t0007g0228a0001c0001t0007g0254others(51): Show | 54 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.1645+1576T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119403973 | ||||||
| chr3:119404019
|
T | G | 1 | a0004c0007t0015g0052 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1645+1622T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119404019 | ||||||
| chr3:119404086
|
A | G | 59 | a0001c0001t0018g0207a0001c0001t0018g0208a0001c0001t0018g0209others(56): Show | 60 | HG00099.hp2 HG00741.hp2 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.1645+1689A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119404086 | ||||||
| chr3:119404100
|
T | C | 22 | a0001c0001t0018g0207a0001c0001t0018g0208a0001c0001t0018g0209others(19): Show | 22 | HG01099.hp1 HG01099.hp2 HG01106.hp2 others(19): Show |
intron_variant | MODIFIER | c.1645+1703T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119404100 | ||||||
| chr3:119404431
|
G | A | 83 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(80): Show | 84 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1645+2034G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119404431 | ||||||
| chr3:119404495
|
G | C | 4 | a0001c0004t0021g0048a0001c0004t0021g0055a0001c0004t0021g0059others(1): Show | 4 | HG02055.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1645+2098G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119404495 | ||||||
| chr3:119404497
|
C | T | 66 | a0001c0001t0018g0207a0001c0001t0018g0208a0001c0001t0018g0209others(63): Show | 67 | HG00099.hp2 HG00741.hp2 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.1645+2100C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119404497 | ||||||
| chr3:119404508
|
T | C | 1 | a0003c0006t0001g0161 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1645+2111T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119404508 | ||||||
| chr3:119404871
|
G | A | 3 | a0001c0001t0039g0260a0001c0001t0045g0286a0001c0001t0052g0283 | 3 | HG02615.hp1 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1645+2474G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119404871 | ||||||
| chr3:119404967
|
C | T | 149 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(146): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.1645+2570C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119404967 | ||||||
| chr3:119405084
|
T | C | 37 | a0001c0004t0003g0007a0001c0004t0003g0021a0001c0004t0003g0024others(34): Show | 38 | HG00099.hp2 HG00741.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1645+2687T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119405084 | ||||||
| chr3:119405093
|
C | A | 1 | a0001c0002t0004g0291 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1645+2696C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119405093 | ||||||
| chr3:119405152
|
T | C | 37 | a0001c0004t0003g0007a0001c0004t0003g0021a0001c0004t0003g0024others(34): Show | 38 | HG00099.hp2 HG00741.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1645+2755T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119405152 | ||||||
| chr3:119405178
|
G | A | 1 | a0001c0001t0060g0026 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1645+2781G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119405178 | ||||||
| chr3:119405311
|
T | C | 7 | a0001c0005t0001g0012a0001c0005t0001g0019a0001c0005t0001g0020others(4): Show | 7 | HG00639.hp1 HG01243.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1645+2914T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119405311 | ||||||
| chr3:119405421
|
C | G | 1 | a0001c0002t0001g0140 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1645+3024C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119405421 | ||||||
| chr3:119405447
|
A | C | 1 | a0001c0001t0025g0204 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1645+3050A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119405447 | ||||||
| chr3:119405652
|
G | A | 1 | a0001c0001t0060g0026 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1645+3255G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119405652 | ||||||
| chr3:119405739
|
T | G | 3 | a0001c0005t0027g0044a0001c0005t0027g0130a0001c0005t0036g0271 | 3 | HG02015.hp2 NA18952.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1645+3342T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119405739 | ||||||
| chr3:119405776
|
T | C | 1 | a0003c0009t0012g0290 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1645+3379T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119405776 | ||||||
| chr3:119406140
|
A | T | 13 | a0001c0004t0059g0015a0003c0006t0001g0159a0003c0006t0001g0161others(10): Show | 13 | HG01099.hp1 HG01099.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.1646-3356A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119406140 | ||||||
| chr3:119406162
|
G | A | 3 | a0001c0002t0001g0023a0001c0002t0001g0171a0001c0002t0004g0230 | 3 | HG00408.hp1 NA18975.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1646-3334G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119406162 | ||||||
| chr3:119406306
|
A | G | 1 | a0009c0017t0019g0185 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1646-3190A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119406306 | ||||||
| chr3:119406355
|
A | C | 40 | a0001c0001t0006g0025a0001c0001t0006g0027a0001c0001t0006g0065others(37): Show | 40 | HG00323.hp1 HG00408.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.1646-3141A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119406355 | ||||||
| chr3:119406483
|
G | A | 1 | a0001c0001t0007g0250 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1646-3013G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119406483 | ||||||
| chr3:119406506
|
T | C | 1 | a0001c0001t0005g0168 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1646-2990T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119406506 | ||||||
| chr3:119406650
|
A | G | 7 | a0004c0007t0015g0016a0004c0007t0015g0030a0004c0007t0015g0052others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1646-2846A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119406650 | ||||||
| chr3:119406856
|
C | T | 3 | a0001c0004t0003g0113a0001c0004t0003g0125a0001c0004t0066g0217 | 3 | HG00741.hp2 HG01256.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1646-2640C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119406856 | ||||||
| chr3:119406975
|
T | C | 191 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(188): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.1646-2521T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119406975 | ||||||
| chr3:119407119
|
G | A | 41 | a0001c0005t0001g0005a0001c0005t0001g0012a0001c0005t0001g0019others(38): Show | 41 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1646-2377G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119407119 | ||||||
| chr3:119407147
|
A | G | 1 | a0001c0005t0014g0028 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1646-2349A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119407147 | ||||||
| chr3:119407150
|
A | G | 1 | a0001c0001t0060g0026 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1646-2346A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119407150 | ||||||
| chr3:119407165
|
A | G | 83 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(80): Show | 84 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1646-2331A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119407165 | ||||||
| chr3:119407297
|
A | C | 1 | a0001c0001t0061g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1646-2199A>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119407297 | ||||||
| chr3:119407355
|
A | AAAAG | 256 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(253): Show | 258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1646-2129_1646-212 others(8): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr3 | 119407355 | |||||
| chr3:119407367
|
GAAAAAAA others(4): Show |
G | 1 | a0001c0001t0061g0057 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1646-2125_1646-211 others(15): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr3 | 119407367 | |||||
| chr3:119407558
|
A | G | 1 | a0001c0001t0008g0178 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1646-1938A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119407558 | ||||||
| chr3:119407603
|
C | G | 41 | a0001c0005t0001g0005a0001c0005t0001g0012a0001c0005t0001g0019others(38): Show | 41 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1646-1893C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119407603 | ||||||
| chr3:119407749
|
C | A | 6 | a0001c0001t0029g0042a0001c0001t0029g0054a0001c0001t0039g0260others(3): Show | 6 | HG02615.hp1 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1646-1747C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119407749 | ||||||
| chr3:119407845
|
A | G | 37 | a0001c0004t0003g0007a0001c0004t0003g0021a0001c0004t0003g0024others(34): Show | 38 | HG00099.hp2 HG00741.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1646-1651A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119407845 | ||||||
| chr3:119407850
|
G | A | 1 | a0001c0001t0007g0275 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1646-1646G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119407850 | ||||||
| chr3:119407869
|
G | A | 1 | a0003c0006t0013g0031 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1646-1627G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119407869 | ||||||
| chr3:119408027
|
CAAGCAAC others(8): Show |
C | 106 | a0001c0001t0006g0025a0001c0001t0006g0027a0001c0001t0006g0065others(103): Show | 107 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1646-1436_1646-142 others(19): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr3 | 119408027 | |||||
| chr3:119408041
|
A | G | 41 | a0001c0005t0001g0005a0001c0005t0001g0012a0001c0005t0001g0019others(38): Show | 41 | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1646-1455A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119408041 | ||||||
| chr3:119408269
|
T | C | 1 | a0002c0003t0002g0145 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1646-1227T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119408269 | ||||||
| chr3:119408465
|
G | A | 1 | a0001c0002t0018g0305 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1646-1031G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119408465 | ||||||
| chr3:119408568
|
A | T | 37 | a0001c0004t0003g0007a0001c0004t0003g0021a0001c0004t0003g0024others(34): Show | 38 | HG00099.hp2 HG00741.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1646-928A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119408568 | ||||||
| chr3:119408831
|
G | A | 46 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(43): Show | 47 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1646-665G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119408831 | ||||||
| chr3:119409036
|
G | A | 106 | a0001c0001t0006g0025a0001c0001t0006g0027a0001c0001t0006g0065others(103): Show | 107 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1646-460G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119409036 | ||||||
| chr3:119409146
|
C | G | 106 | a0001c0001t0006g0025a0001c0001t0006g0027a0001c0001t0006g0065others(103): Show | 107 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1646-350C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119409146 | ||||||
| chr3:119409168
|
C | A | 37 | a0001c0004t0003g0007a0001c0004t0003g0021a0001c0004t0003g0024others(34): Show | 38 | HG00099.hp2 HG00741.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1646-328C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119409168 | ||||||
| chr3:119409457
|
G | A | 1 | a0001c0001t0020g0043 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1646-39G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | chr3 | 119409457 | ||||||
| chr3:119409781
|
A | G | 200 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(197): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
splice_region_variant&intron_variant | LOW | c.1926+5A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119409781 | ||||||
| chr3:119409787
|
T | C | 152 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(149): Show | 154 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.1926+11T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119409787 | ||||||
| chr3:119409789
|
C | A | 2 | a0001c0002t0001g0101a0001c0002t0001g0134 | 2 | NA18944.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1926+13C>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119409789 | ||||||
| chr3:119409863
|
A | T | 46 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(43): Show | 47 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1926+87A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119409863 | ||||||
| chr3:119409864
|
AT | A | 46 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(43): Show | 47 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1926+97delT | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr3 | 119409864 | |||||
| chr3:119409865
|
T | A | 99 | a0001c0001t0006g0025a0001c0001t0006g0027a0001c0001t0006g0065others(96): Show | 100 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1926+89T>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119409865 | ||||||
| chr3:119409939
|
T | G | 6 | a0001c0005t0014g0009a0001c0005t0014g0028a0001c0005t0014g0047others(3): Show | 6 | HG02280.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1926+163T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119409939 | ||||||
| chr3:119410335
|
C | G | 1 | a0001c0001t0006g0094 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1926+559C>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119410335 | ||||||
| chr3:119410476
|
G | A | 62 | a0001c0001t0006g0025a0001c0001t0006g0027a0001c0001t0006g0065others(59): Show | 62 | HG00323.hp1 HG00408.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.1926+700G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119410476 | ||||||
| chr3:119410681
|
T | C | 46 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(43): Show | 47 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1926+905T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119410681 | ||||||
| chr3:119410956
|
G | A | 106 | a0001c0001t0006g0025a0001c0001t0006g0027a0001c0001t0006g0065others(103): Show | 107 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1926+1180G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119410956 | ||||||
| chr3:119411100
|
T | C | 7 | a0004c0007t0015g0016a0004c0007t0015g0030a0004c0007t0015g0052others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1926+1324T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119411100 | ||||||
| chr3:119411120
|
T | G | 6 | a0001c0001t0029g0042a0001c0001t0029g0054a0001c0001t0039g0260others(3): Show | 6 | HG02615.hp1 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1926+1344T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119411120 | ||||||
| chr3:119411273
|
T | C | 300 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(297): Show | 302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.1926+1497T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119411273 | ||||||
| chr3:119411294
|
G | A | 51 | a0001c0002t0001g0008a0001c0002t0001g0014a0001c0002t0001g0023others(48): Show | 51 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.1926+1518G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119411294 | ||||||
| chr3:119411305
|
G | T | 4 | a0004c0007t0015g0016a0004c0007t0015g0052a0004c0007t0044g0196others(1): Show | 4 | HG01884.hp1 HG02258.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1926+1529G>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119411305 | ||||||
| chr3:119411405
|
T | C | 46 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(43): Show | 47 | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1926+1629T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119411405 | ||||||
| chr3:119411424
|
T | C | 9 | a0001c0005t0001g0005a0001c0005t0001g0049a0001c0005t0014g0009others(6): Show | 9 | HG00735.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1926+1648T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119411424 | ||||||
| chr3:119411513
|
A | G | 186 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(183): Show | 188 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.1926+1737A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119411513 | ||||||
| chr3:119411526
|
G | A | 52 | a0001c0001t0006g0025a0001c0001t0006g0027a0001c0001t0006g0065others(49): Show | 52 | HG00323.hp1 HG00408.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.1926+1750G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119411526 | ||||||
| chr3:119411609
|
C | T | 94 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(91): Show | 95 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1926+1833C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119411609 | ||||||
| chr3:119411655
|
C | T | 1 | a0001c0001t0005g0022 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1926+1879C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119411655 | ||||||
| chr3:119411796
|
A | G | 2 | a0001c0002t0004g0256a0001c0002t0012g0206 | 2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1926+2020A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119411796 | ||||||
| chr3:119412018
|
A | G | 1 | a0001c0004t0003g0150 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1927-1838A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119412018 | ||||||
| chr3:119412205
|
A | G | 1 | a0001c0001t0011g0186 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1927-1651A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119412205 | ||||||
| chr3:119412354
|
C | T | 1 | a0001c0004t0032g0071 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1927-1502C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119412354 | ||||||
| chr3:119412391
|
C | CA | 36 | a0001c0001t0006g0025a0001c0001t0006g0065a0001c0001t0006g0066others(33): Show | 36 | HG00408.hp2 HG01071.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.1927-1452dupA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr3 | 119412391 | |||||
| chr3:119412402
|
AAAG | A | 6 | a0001c0001t0006g0027a0001c0001t0006g0100a0001c0001t0006g0148others(3): Show | 6 | HG00323.hp1 HG01099.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1927-1451_1927-144 others(7): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr3 | 119412402 | |||||
| chr3:119412406
|
AAAAG | A | 46 | a0001c0001t0018g0207a0001c0001t0018g0208a0001c0001t0018g0209others(43): Show | 47 | HG00099.hp2 HG00741.hp2 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.1927-1438_1927-143 others(8): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr3 | 119412406 | |||||
| chr3:119412409
|
A | G | 6 | a0001c0001t0006g0027a0001c0001t0006g0100a0001c0001t0006g0148others(3): Show | 6 | HG00323.hp1 HG01099.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1927-1447A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119412409 | ||||||
| chr3:119412410
|
G | A | 6 | a0001c0001t0006g0027a0001c0001t0006g0100a0001c0001t0006g0148others(3): Show | 6 | HG00323.hp1 HG01099.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.1927-1446G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119412410 | ||||||
| chr3:119412456
|
C | T | 7 | a0004c0007t0015g0016a0004c0007t0015g0030a0004c0007t0015g0052others(4): Show | 7 | HG01884.hp1 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1927-1400C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119412456 | ||||||
| chr3:119412473
|
T | C | 38 | a0001c0004t0003g0007a0001c0004t0003g0021a0001c0004t0003g0024others(35): Show | 39 | HG00099.hp2 HG00741.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.1927-1383T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119412473 | ||||||
| chr3:119412540
|
G | A | 5 | a0001c0001t0025g0204a0001c0001t0025g0223a0001c0001t0042g0282others(2): Show | 5 | HG00280.hp1 HG01081.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1927-1316G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119412540 | ||||||
| chr3:119412548
|
A | G | 1 | a0001c0001t0017g0175 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1927-1308A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119412548 | ||||||
| chr3:119412648
|
T | G | 7 | a0001c0002t0001g0108a0001c0002t0001g0135a0001c0002t0001g0173others(4): Show | 7 | NA18950.hp1 NA18999.hp2 NA19003.hp2 others(4): Show |
intron_variant | MODIFIER | c.1927-1208T>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119412648 | ||||||
| chr3:119412825
|
A | T | 4 | a0001c0004t0021g0048a0001c0004t0021g0055a0001c0004t0021g0059others(1): Show | 4 | HG02055.hp1 HG02922.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1927-1031A>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119412825 | ||||||
| chr3:119413005
|
G | A | 1 | a0012c0015t0035g0237 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1927-851G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119413005 | ||||||
| chr3:119413075
|
T | C | 5 | a0001c0001t0025g0204a0001c0001t0025g0223a0001c0001t0042g0282others(2): Show | 5 | HG00280.hp1 HG01081.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1927-781T>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119413075 | ||||||
| chr3:119413080
|
G | A | 11 | a0002c0003t0002g0032a0002c0003t0002g0118a0002c0003t0002g0152others(8): Show | 11 | HG00280.hp2 HG00621.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.1927-776G>A | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119413080 | ||||||
| chr3:119413132
|
A | G | 6 | a0001c0001t0029g0042a0001c0001t0029g0054a0001c0001t0039g0260others(3): Show | 6 | HG02615.hp1 HG02630.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1927-724A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119413132 | ||||||
| chr3:119413207
|
C | T | 4 | a0001c0001t0005g0087a0001c0001t0007g0275a0001c0001t0007g0296others(1): Show | 4 | HG00735.hp1 HG00738.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1927-649C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119413207 | ||||||
| chr3:119413247
|
A | G | 47 | a0001c0001t0018g0207a0001c0001t0018g0208a0001c0001t0018g0209others(44): Show | 48 | HG00099.hp2 HG00741.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.1927-609A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119413247 | ||||||
| chr3:119413301
|
C | T | 258 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(255): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.1927-555C>T | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119413301 | ||||||
| chr3:119413316
|
C | CA | 54 | a0001c0001t0018g0207a0001c0001t0018g0208a0001c0001t0018g0209others(51): Show | 55 | HG00099.hp2 HG00741.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.1927-523dupA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr3 | 119413316 | |||||
| chr3:119413316
|
CA | C | 8 | a0001c0001t0005g0142a0001c0001t0008g0200a0001c0002t0003g0144others(5): Show | 8 | HG01106.hp2 HG01884.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1927-523delA | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr3 | 119413316 | |||||
| chr3:119413663
|
A | G | 2 | a0001c0005t0001g0160a0001c0005t0004g0253 | 2 | HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1927-193A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119413663 | ||||||
| chr3:119413707
|
A | G | 251 | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(248): Show | 253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1927-149A>G | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119413707 | ||||||
| chr3:119413769
|
G | C | 1 | a0003c0006t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1927-87G>C | ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | chr3 | 119413769 |