| geneid | 8874 |
|---|---|
| ensemblid | ENSG00000102606.20 |
| hgncid | 15607 |
| symbol | ARHGEF7 |
| name | Rho guanine nucleotide exchange factor 7 |
| refseq_nuc | NM_001354046.2 |
| refseq_prot | NP_001340975.1 |
| ensembl_nuc | ENST00000646102.2 |
| ensembl_prot | ENSP00000495631.1 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 111115310 |
| end | 111305732 |
| strand | + |
| ver | v1.2 |
| region | chr13:111115310-111305732 |
| region5000 | chr13:111110310-111310732 |
| regionname0 | ARHGEF7_chr13_111115310_111305732 |
| regionname5000 | ARHGEF7_chr13_111110310_111310732 |
| 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 | 1/1 | 862 | 267 | 83 | 59 | 83 | 14 | 26 | 73 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0002 | 0/0 | 862 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0003 | 0/0 | 862 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0004 | 0/0 | 862 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0005 | 0/0 | 862 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0006 | 0/0 | 862 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0007 | 0/0 | 862 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| 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 | 1/0 | 2589 | 201 | 74 | 46 | 47 | 11 | 22 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| c0002 | 0/0 | 2589 | 47 | 0 | 6 | 34 | 3 | 4 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| c0003 | 0/0 | 2589 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| c0004 | 0/0 | 2589 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| c0005 | 0/1 | 2589 | 2 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| c0006 | 0/0 | 2589 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| c0007 | 0/0 | 2589 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| c0008 | 0/0 | 2589 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| c0009 | 0/0 | 2589 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| c0010 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| c0011 | 0/0 | 2589 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| c0012 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| c0013 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| c0014 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| c0015 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| c0016 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| c0017 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| c0018 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| c0019 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| 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 | 2837 | 67 | 21 | 18 | 11 | 7 | 10 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0002 | 0/0 | 2837 | 46 | 6 | 4 | 28 | 3 | 5 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0003 | 0/0 | 2837 | 33 | 8 | 8 | 6 | 2 | 9 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0004 | 1/0 | 2837 | 25 | 6 | 2 | 11 | 2 | 3 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0005 | 0/0 | 2837 | 14 | 1 | 12 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0006 | 0/0 | 2843 | 12 | 1 | 3 | 8 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0007 | 0/0 | 2837 | 10 | 10 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0008 | 0/0 | 2837 | 7 | 6 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0009 | 0/0 | 2843 | 7 | 0 | 0 | 7 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0010 | 0/0 | 2837 | 6 | 0 | 0 | 6 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0011 | 0/0 | 2837 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0012 | 0/0 | 2837 | 4 | 2 | 2 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0013 | 0/0 | 2840 | 3 | 0 | 3 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0014 | 0/0 | 2846 | 3 | 0 | 3 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0015 | 0/0 | 2837 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0016 | 0/0 | 2837 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0017 | 0/0 | 2837 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0018 | 0/0 | 2837 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0019 | 0/0 | 2837 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0020 | 0/1 | 2837 | 2 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0021 | 0/0 | 2837 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0022 | 0/0 | 2837 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0023 | 0/0 | 2837 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0024 | 0/0 | 2840 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0025 | 0/0 | 2840 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0026 | 0/0 | 2837 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0027 | 0/0 | 2837 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0028 | 0/0 | 2837 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0029 | 0/0 | 2837 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0030 | 0/0 | 2837 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0031 | 0/0 | 2837 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0032 | 0/0 | 2837 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0033 | 0/0 | 2837 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| t0034 | 0/0 | 2837 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| 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 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0026 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| 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 | 1/0 | 2589 | 201 | 74 | 46 | 47 | 11 | 22 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0002 | 0/0 | 2589 | 47 | 0 | 6 | 34 | 3 | 4 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0003 | 0/0 | 2589 | 4 | 4 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0004 | 0/0 | 2589 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0005 | 0/1 | 2589 | 2 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0006 | 0/0 | 2589 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0007 | 0/0 | 2589 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0008 | 0/0 | 2589 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0012 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0013 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0014 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0015 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0016 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0002c0009 | 0/0 | 2589 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0003c0011 | 0/0 | 2589 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0004c0017 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0005c0018 | 0/0 | 2589 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0006c0019 | 0/0 | 2589 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0007c0010 | 0/0 | 2589 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5425 | 59 | 19 | 13 | 10 | 7 | 10 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0002 | 0/0 | 5425 | 8 | 3 | 0 | 5 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0003 | 0/0 | 5425 | 30 | 6 | 8 | 6 | 2 | 8 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0004 | 1/0 | 5425 | 24 | 5 | 2 | 11 | 2 | 3 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0005 | 0/0 | 5425 | 13 | 1 | 12 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0006 | 0/0 | 5431 | 11 | 1 | 3 | 7 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0007 | 0/0 | 5425 | 10 | 10 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0008 | 0/0 | 5425 | 6 | 5 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0009 | 0/0 | 5431 | 7 | 0 | 0 | 7 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0011 | 0/0 | 5425 | 6 | 6 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0012 | 0/0 | 5425 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0013 | 0/0 | 5428 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0014 | 0/0 | 5434 | 3 | 0 | 3 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0015 | 0/0 | 5425 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0016 | 0/0 | 5425 | 3 | 3 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0017 | 0/0 | 5425 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0018 | 0/0 | 5425 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0019 | 0/0 | 5425 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0023 | 0/0 | 5425 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0025 | 0/0 | 5428 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0026 | 0/0 | 5425 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0028 | 0/0 | 5425 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0029 | 0/0 | 5425 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0032 | 0/0 | 5425 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0033 | 0/0 | 5425 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0001t0034 | 0/0 | 5425 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0002t0001 | 0/0 | 5425 | 2 | 0 | 1 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0002t0002 | 0/0 | 5425 | 34 | 0 | 4 | 23 | 3 | 4 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0002t0006 | 0/0 | 5431 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0002t0010 | 0/0 | 5425 | 6 | 0 | 0 | 6 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0002t0021 | 0/0 | 5425 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0002t0024 | 0/0 | 5428 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0002t0031 | 0/0 | 5425 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0003t0001 | 0/0 | 5425 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0003t0003 | 0/0 | 5425 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0003t0019 | 0/0 | 5425 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0004t0022 | 0/0 | 5425 | 2 | 0 | 0 | 2 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0005t0020 | 0/1 | 5425 | 2 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0006t0012 | 0/0 | 5425 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0007t0004 | 0/0 | 5425 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0007t0027 | 0/0 | 5425 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0008t0001 | 0/0 | 5425 | 2 | 0 | 2 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0012t0030 | 0/0 | 5425 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0013t0001 | 0/0 | 5425 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0014t0001 | 0/0 | 5425 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0015t0002 | 0/0 | 5425 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0001c0016t0008 | 0/0 | 5425 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0002c0009t0002 | 0/0 | 5425 | 2 | 2 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0003c0011t0005 | 0/0 | 5425 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0004c0017t0003 | 0/0 | 5425 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0005c0018t0013 | 0/0 | 5428 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0006c0019t0002 | 0/0 | 5425 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| a0007c0010t0001 | 0/0 | 5425 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | copy fasta | chr13 | 111110310 | 111310732 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0026 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0005g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0005g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0006g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0006g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0006g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0006g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0006g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0006g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0007g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0007g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0008g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0008g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0008g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0008g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0008g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0009g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0009g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0009g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0009g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0009g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0009g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0009g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0011g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0011g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0011g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0011g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0011g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0011g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0012g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0012g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0013g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0013g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0014g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0014g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0014g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0015g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0015g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0015g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0016g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0016g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0016g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0017g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0017g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0018g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0018g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0019g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0023g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0023g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0025g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0026g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0028g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0029g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0032g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0033g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0001t0034g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0006g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0010g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0010g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0010g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0010g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0010g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0010g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0021g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0021g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0024g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0002t0031g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0003t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0003t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0003t0019g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0004t0022g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0004t0022g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0005t0020g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0005t0020g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0006t0012g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0006t0012g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0007t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0007t0027g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0008t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0008t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0012t0030g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0013t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0014t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0015t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0001c0016t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0002c0009t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0002c0009t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0003c0011t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0004c0017t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0005c0018t0013g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0006c0019t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| a0007c0010t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0219 | EUR | GBR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0104 | EUR | GBR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0216 | EUR | GBR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | GBR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0248 | EUR | FIN | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0247 | EUR | FIN | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00323 | hp2 | a0001 | c0002 | t0002 | g0206 | EUR | FIN | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | CHS | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00558 | hp2 | a0001 | c0001 | t0006 | g0032 | EAS | CHS | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | CHS | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0221 | EAS | CHS | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00642 | hp1 | a0001 | c0001 | t0013 | g0162 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00642 | hp2 | a0001 | c0013 | t0001 | g0100 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0119 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00738 | hp2 | a0001 | c0001 | t0025 | g0176 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00741 | hp1 | a0001 | c0006 | t0012 | g0121 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01069 | hp1 | a0001 | c0008 | t0001 | g0098 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01069 | hp2 | a0005 | c0018 | t0013 | g0187 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0230 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01071 | hp2 | a0001 | c0008 | t0001 | g0109 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0114 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01081 | hp2 | a0001 | c0006 | t0012 | g0124 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01109 | hp1 | a0001 | c0001 | t0008 | g0017 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0102 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01167 | hp2 | a0001 | c0001 | t0034 | g0061 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0103 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0147 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01175 | hp2 | a0001 | c0001 | t0005 | g0063 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01192 | hp1 | a0001 | c0014 | t0001 | g0058 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01243 | hp1 | a0001 | c0005 | t0020 | g0117 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01257 | hp1 | a0001 | c0002 | t0024 | g0183 | AMR | CLM | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0141 | AMR | CLM | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | CLM | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0222 | AMR | CLM | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01346 | hp2 | a0001 | c0001 | t0006 | g0268 | AMR | CLM | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0140 | AMR | CLM | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0148 | AMR | CLM | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0139 | AMR | CLM | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0198 | EUR | IBS | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0181 | EUR | IBS | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01884 | hp1 | a0001 | c0001 | t0011 | g0006 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0067 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0136 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01928 | hp1 | a0001 | c0001 | t0014 | g0186 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0262 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01943 | hp1 | a0001 | c0002 | t0002 | g0265 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01943 | hp2 | a0001 | c0001 | t0014 | g0153 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0128 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01978 | hp1 | a0001 | c0001 | t0005 | g0116 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0266 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01981 | hp1 | a0001 | c0001 | t0005 | g0115 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0267 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01993 | hp1 | a0001 | c0002 | t0002 | g0149 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01993 | hp2 | a0001 | c0001 | t0013 | g0154 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0263 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0165 | EAS | KHV | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | KHV | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02055 | hp1 | a0001 | c0001 | t0011 | g0055 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0261 | EAS | KHV | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0150 | EAS | KHV | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | KHV | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0239 | EAS | KHV | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0223 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02148 | hp2 | a0001 | c0001 | t0014 | g0161 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02257 | hp1 | a0001 | c0003 | t0003 | g0146 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02258 | hp1 | a0001 | c0001 | t0011 | g0007 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02280 | hp2 | a0001 | c0001 | t0016 | g0077 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02293 | hp1 | a0001 | c0001 | t0005 | g0212 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02293 | hp2 | a0001 | c0001 | t0005 | g0126 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0170 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02300 | hp2 | a0001 | c0001 | t0006 | g0042 | AMR | PEL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02451 | hp1 | a0001 | c0003 | t0003 | g0021 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02451 | hp2 | a0001 | c0001 | t0017 | g0269 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02615 | hp1 | a0001 | c0001 | t0028 | g0127 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0064 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0090 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0110 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0065 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0145 | SAS | PJL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02717 | hp1 | a0001 | c0001 | t0015 | g0272 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0226 | SAS | PJL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0089 | SAS | PJL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02738 | hp2 | a0001 | c0001 | t0032 | g0030 | SAS | PJL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0111 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02809 | hp2 | a0001 | c0001 | t0017 | g0270 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0015 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0094 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02895 | hp1 | a0001 | c0001 | t0016 | g0012 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02895 | hp2 | a0001 | c0001 | t0011 | g0075 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | ESN | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02922 | hp2 | a0001 | c0001 | t0016 | g0143 | AFR | ESN | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0122 | AFR | ESN | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0004 | AFR | ESN | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02976 | hp2 | a0001 | c0012 | t0030 | g0072 | AFR | ESN | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03041 | hp1 | a0001 | c0001 | t0011 | g0070 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0073 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03098 | hp1 | a0001 | c0001 | t0019 | g0071 | AFR | MSL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0142 | AFR | MSL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03130 | hp1 | a0001 | c0015 | t0002 | g0023 | AFR | ESN | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03139 | hp1 | a0001 | c0007 | t0004 | g0059 | AFR | ESN | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0132 | AFR | ESN | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0057 | AFR | ESN | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03195 | hp2 | a0001 | c0001 | t0033 | g0101 | AFR | ESN | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03209 | hp1 | a0001 | c0001 | t0012 | g0013 | AFR | MSL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03225 | hp2 | a0001 | c0001 | t0018 | g0038 | AFR | MSL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03453 | hp2 | a0001 | c0001 | t0015 | g0271 | AFR | MSL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03486 | hp1 | a0002 | c0009 | t0002 | g0069 | AFR | MSL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03486 | hp2 | a0007 | c0010 | t0001 | g0095 | AFR | MSL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0169 | SAS | PJL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | ESN | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0034 | AFR | GWD | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03579 | hp1 | a0002 | c0009 | t0002 | g0112 | AFR | MSL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | MSL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0060 | SAS | PJL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0179 | SAS | PJL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03669 | hp2 | a0006 | c0019 | t0002 | g0175 | SAS | PJL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0228 | SAS | PJL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0085 | SAS | PJL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0194 | SAS | PJL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0274 | SAS | BEB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03942 | hp1 | a0004 | c0017 | t0003 | g0120 | SAS | BEB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0254 | SAS | STU | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG04115 | hp2 | a0001 | c0002 | t0002 | g0166 | SAS | STU | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0087 | SAS | BEB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18522 | hp2 | a0001 | c0001 | t0015 | g0273 | AFR | YRI | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18906 | hp1 | a0001 | c0001 | t0018 | g0020 | AFR | YRI | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0035 | AFR | YRI | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18939 | hp1 | a0001 | c0001 | t0006 | g0083 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18939 | hp2 | a0001 | c0004 | t0022 | g0209 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18941 | hp2 | a0001 | c0001 | t0029 | g0201 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0189 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18950 | hp2 | a0001 | c0001 | t0006 | g0234 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18952 | hp1 | a0001 | c0002 | t0010 | g0192 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18957 | hp1 | a0001 | c0002 | t0021 | g0255 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18962 | hp2 | a0001 | c0001 | t0009 | g0202 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18966 | hp2 | a0001 | c0001 | t0006 | g0185 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18968 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18968 | hp2 | a0001 | c0002 | t0010 | g0159 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18971 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18974 | hp2 | a0001 | c0001 | t0006 | g0246 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18979 | hp1 | a0001 | c0002 | t0021 | g0256 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0157 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18982 | hp1 | a0001 | c0001 | t0009 | g0250 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0046 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18988 | hp2 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0158 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18999 | hp1 | a0001 | c0001 | t0006 | g0041 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18999 | hp2 | a0001 | c0002 | t0010 | g0081 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19000 | hp1 | a0001 | c0001 | t0009 | g0258 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19005 | hp2 | a0001 | c0001 | t0009 | g0259 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19010 | hp1 | a0003 | c0011 | t0005 | g0191 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19010 | hp2 | a0001 | c0002 | t0031 | g0130 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19011 | hp1 | a0001 | c0002 | t0010 | g0163 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19011 | hp2 | a0001 | c0001 | t0006 | g0218 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0252 | AFR | LWK | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19043 | hp2 | a0001 | c0016 | t0008 | g0227 | AFR | LWK | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0190 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19056 | hp2 | a0001 | c0004 | t0022 | g0208 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19063 | hp1 | a0001 | c0002 | t0010 | g0080 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19063 | hp2 | a0001 | c0002 | t0010 | g0197 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19075 | hp2 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19076 | hp1 | a0001 | c0001 | t0009 | g0214 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19076 | hp2 | a0001 | c0002 | t0002 | g0079 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19077 | hp2 | a0001 | c0001 | t0009 | g0260 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19079 | hp1 | a0001 | c0001 | t0009 | g0171 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19088 | hp2 | a0001 | c0002 | t0006 | g0236 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19240 | hp1 | a0001 | c0001 | t0011 | g0076 | AFR | YRI | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA19240 | hp2 | a0001 | c0007 | t0027 | g0054 | AFR | YRI | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ASW | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA20129 | hp2 | a0001 | c0001 | t0026 | g0053 | AFR | ASW | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | TSI | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0229 | EUR | TSI | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0224 | SAS | GIH | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0210 | SAS | GIH | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0264 | AMR | CLM | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02109 | hp1 | a0001 | c0001 | t0023 | g0036 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0225 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02559 | hp1 | a0001 | c0001 | t0023 | g0037 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG02559 | hp2 | a0001 | c0003 | t0019 | g0022 | AFR | ACB | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03471 | hp1 | a0001 | c0001 | t0012 | g0001 | AFR | MSL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| HG03471 | hp2 | a0001 | c0001 | t0008 | g0003 | AFR | MSL | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA20300 | hp1 | a0001 | c0001 | t0007 | g0028 | AFR | USA | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | USA | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | LWK | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0005 | t0020 | g0118 | REF | REF | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0026 | REF | REF | ARHGEF7_chr13_111110310_111310732 | ARHGEF7 | chr13 | 111110310 | 111310732 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:111115611
|
G | A | 1 | a0007 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.85G>A | p.Gly29Ser | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/22 | 302/5425 | 85/2589 | 29/862 | chr13 | 111115611 | ||
| chr13:111115624
|
C | T | 1 | a0006 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.98C>T | p.Ala33Val | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/22 | 315/5425 | 98/2589 | 33/862 | chr13 | 111115624 | ||
| chr13:111209950
|
A | T | 1 | a0002 | 2 | HG03486.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.416A>T | p.Gln139Leu | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/22 | 633/5425 | 416/2589 | 139/862 | chr13 | 111209950 | ||
| chr13:111209964
|
C | T | 1 | a0005 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.430C>T | p.Arg144Trp | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/22 | 647/5425 | 430/2589 | 144/862 | chr13 | 111209964 | ||
| chr13:111217801
|
G | C | 1 | a0003 | 1 | NA19010.hp1 | missense_variant | MODERATE | c.591G>C | p.Glu197Asp | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/22 | 808/5425 | 591/2589 | 197/862 | chr13 | 111217801 | ||
| chr13:111267661
|
C | T | 1 | a0004 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.1064C>T | p.Thr355Met | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/22 | 1281/5425 | 1064/2589 | 355/862 | chr13 | 111267661 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:111217690
|
T | C | 2 | a0001c0002a0006c0019 | 48 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(45): Show |
synonymous_variant | LOW | c.480T>C | p.Asp160Asp | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/22 | 697/5425 | 480/2589 | 160/862 | chr13 | 111217690 | ||
| chr13:111217879
|
C | T | 1 | a0001c0008 | 2 | HG01069.hp1 HG01071.hp2 |
splice_region_variant&synonymous_variant | LOW | c.669C>T | p.Ser223Ser | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/22 | 886/5425 | 669/2589 | 223/862 | chr13 | 111217879 | ||
| chr13:111244259
|
G | A | 1 | a0001c0004 | 2 | NA18939.hp2 NA19056.hp2 |
synonymous_variant | LOW | c.915G>A | p.Gln305Gln | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/22 | 1132/5425 | 915/2589 | 305/862 | chr13 | 111244259 | ||
| chr13:111267623
|
G | A | 1 | a0001c0012 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.1026G>A | p.Thr342Thr | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/22 | 1243/5425 | 1026/2589 | 342/862 | chr13 | 111267623 | ||
| chr13:111267659
|
C | G | 1 | a0001c0003 | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
synonymous_variant | LOW | c.1062C>G | p.Leu354Leu | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/22 | 1279/5425 | 1062/2589 | 354/862 | chr13 | 111267659 | ||
| chr13:111277626
|
T | C | 1 | a0001c0013 | 1 | HG00642.hp2 | synonymous_variant | LOW | c.1459T>C | p.Leu487Leu | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/22 | 1676/5425 | 1459/2589 | 487/862 | chr13 | 111277626 | ||
| chr13:111280566
|
G | A | 1 | a0001c0005 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
synonymous_variant | LOW | c.1614G>A | p.Ser538Ser | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/22 | 1831/5425 | 1614/2589 | 538/862 | chr13 | 111280566 | ||
| chr13:111283171
|
G | A | 1 | a0001c0014 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.1758G>A | p.Lys586Lys | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/22 | 1975/5425 | 1758/2589 | 586/862 | chr13 | 111283171 | ||
| chr13:111283189
|
C | T | 1 | a0001c0007 | 2 | HG03139.hp1 NA19240.hp2 |
synonymous_variant | LOW | c.1776C>T | p.Pro592Pro | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/22 | 1993/5425 | 1776/2589 | 592/862 | chr13 | 111283189 | ||
| chr13:111283324
|
G | A | 1 | a0001c0015 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.1911G>A | p.Ala637Ala | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/22 | 2128/5425 | 1911/2589 | 637/862 | chr13 | 111283324 | ||
| chr13:111286164
|
T | C | 1 | a0001c0006 | 2 | HG00741.hp1 HG01081.hp2 |
synonymous_variant | LOW | c.1968T>C | p.Pro656Pro | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/22 | 2185/5425 | 1968/2589 | 656/862 | chr13 | 111286164 | ||
| chr13:111303044
|
C | T | 1 | a0001c0016 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.2520C>T | p.Asp840Asp | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 2737/5425 | 2520/2589 | 840/862 | chr13 | 111303044 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:111115434
|
A | AGGC | 5 | a0001c0001t0013a0001c0001t0014a0001c0001t0025others(2): Show | 8 | HG00642.hp1 HG00738.hp2 HG01069.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-75_-73dupCGG | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/22 | 72 | INFO_REALIGN_3_PRIME | chr13 | 111115434 | ||||
| chr13:111115464
|
G | A | 2 | a0001c0001t0015a0001c0001t0017 | 5 | HG02451.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-63G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/22 | 63 | chr13 | 111115464 | |||||
| chr13:111115525
|
C | A | 2 | a0001c0001t0026a0001c0007t0027 | 2 | NA19240.hp2 NA20129.hp2 |
5_prime_UTR_variant | MODIFIER | c.-2C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/22 | 2 | chr13 | 111115525 | |||||
| chr13:111303118
|
T | C | 49 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
3_prime_UTR_variant | MODIFIER | c.*5T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 5 | chr13 | 111303118 | |||||
| chr13:111303119
|
G | A | 2 | a0001c0001t0008a0001c0016t0008 | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 6 | chr13 | 111303119 | |||||
| chr13:111303338
|
A | G | 1 | a0001c0001t0034 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*225A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 225 | chr13 | 111303338 | |||||
| chr13:111303560
|
T | C | 39 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(36): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*447T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 447 | chr13 | 111303560 | |||||
| chr13:111303566
|
G | A | 1 | a0001c0001t0028 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*453G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 453 | chr13 | 111303566 | |||||
| chr13:111303595
|
C | T | 1 | a0001c0002t0010 | 6 | NA18952.hp1 NA18968.hp2 NA18999.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*482C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 482 | chr13 | 111303595 | |||||
| chr13:111303756
|
A | G | 16 | a0001c0001t0002a0001c0001t0003a0001c0001t0012others(13): Show | 97 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*643A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 643 | chr13 | 111303756 | |||||
| chr13:111303770
|
A | G | 2 | a0001c0001t0012a0001c0006t0012 | 4 | HG00741.hp1 HG01081.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*657A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 657 | chr13 | 111303770 | |||||
| chr13:111303788
|
A | G | 2 | a0001c0001t0008a0001c0016t0008 | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*675A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 675 | chr13 | 111303788 | |||||
| chr13:111303812
|
G | A | 1 | a0001c0001t0029 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*699G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 699 | chr13 | 111303812 | |||||
| chr13:111303835
|
C | T | 2 | a0001c0001t0008a0001c0016t0008 | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*722C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 722 | chr13 | 111303835 | |||||
| chr13:111303839
|
T | C | 1 | a0001c0001t0018 | 2 | HG03225.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*726T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 726 | chr13 | 111303839 | |||||
| chr13:111303960
|
G | T | 2 | a0001c0001t0007a0001c0001t0023 | 12 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*847G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 847 | chr13 | 111303960 | |||||
| chr13:111304269
|
C | T | 1 | a0001c0001t0032 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1156C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 1156 | chr13 | 111304269 | |||||
| chr13:111304270
|
G | A | 2 | a0001c0001t0019a0001c0003t0019 | 2 | HG02559.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1157G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 1157 | chr13 | 111304270 | |||||
| chr13:111304270
|
G | T | 3 | a0001c0001t0029a0001c0002t0021a0001c0002t0031 | 4 | NA18941.hp2 NA18957.hp1 NA18979.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1157G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 1157 | chr13 | 111304270 | |||||
| chr13:111304310
|
G | C | 2 | a0001c0001t0011a0001c0001t0026 | 7 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1197G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 1197 | chr13 | 111304310 | |||||
| chr13:111304345
|
T | C | 3 | a0001c0001t0016a0001c0001t0034a0001c0012t0030 | 5 | HG01167.hp2 HG02280.hp2 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1232T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 1232 | chr13 | 111304345 | |||||
| chr13:111304434
|
A | G | 1 | a0001c0005t0020 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1321A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 1321 | chr13 | 111304434 | |||||
| chr13:111304460
|
C | CTATCTT | 4 | a0001c0001t0006a0001c0001t0009a0001c0001t0014others(1): Show | 22 | HG00558.hp2 HG01346.hp2 HG01928.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1350_*1355dupTCTT others(2): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 1356 | INFO_REALIGN_3_PRIME | chr13 | 111304460 | ||||
| chr13:111304630
|
G | C | 2 | a0001c0001t0008a0001c0016t0008 | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1517G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 1517 | chr13 | 111304630 | |||||
| chr13:111304667
|
T | C | 2 | a0001c0001t0008a0001c0016t0008 | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1554T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 1554 | chr13 | 111304667 | |||||
| chr13:111304704
|
T | C | 2 | a0001c0001t0008a0001c0016t0008 | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1591T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 1591 | chr13 | 111304704 | |||||
| chr13:111304810
|
T | C | 1 | a0001c0002t0021 | 2 | NA18957.hp1 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1697T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 1697 | chr13 | 111304810 | |||||
| chr13:111304901
|
C | T | 1 | a0001c0012t0030 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1788C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 1788 | chr13 | 111304901 | |||||
| chr13:111305016
|
C | T | 1 | a0001c0001t0009 | 7 | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1903C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 1903 | chr13 | 111305016 | |||||
| chr13:111305103
|
C | T | 1 | a0001c0004t0022 | 2 | NA18939.hp2 NA19056.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1990C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 1990 | chr13 | 111305103 | |||||
| chr13:111305180
|
G | T | 2 | a0001c0001t0008a0001c0016t0008 | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2067G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 2067 | chr13 | 111305180 | |||||
| chr13:111305522
|
G | A | 6 | a0001c0001t0002a0001c0002t0002a0001c0002t0010others(3): Show | 52 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*2409G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 2409 | chr13 | 111305522 | |||||
| chr13:111305610
|
C | T | 1 | a0001c0001t0033 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2497C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 2497 | chr13 | 111305610 | |||||
| chr13:111305614
|
T | C | 2 | a0001c0001t0008a0001c0016t0008 | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2501T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 2501 | chr13 | 111305614 | |||||
| chr13:111305658
|
A | G | 1 | a0001c0001t0023 | 2 | HG02109.hp1 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2545A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 22/22 | 2545 | chr13 | 111305658 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:111115842
|
T | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0007g0004others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+151T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111115842 | ||||||
| chr13:111115896
|
A | AG | 5 | a0001c0001t0002g0029a0001c0001t0006g0032a0001c0001t0032g0030others(2): Show | 5 | HG00558.hp1 HG00558.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+206dupG | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111115896 | |||||
| chr13:111115898
|
C | G | 252 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0039others(249): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.165+207C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111115898 | ||||||
| chr13:111115984
|
C | G | 1 | a0001c0001t0003g0274 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.165+293C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111115984 | ||||||
| chr13:111116024
|
C | G | 131 | a0001c0001t0001g0160a0001c0001t0001g0167a0001c0001t0001g0168others(128): Show | 131 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.165+333C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111116024 | ||||||
| chr13:111116060
|
C | T | 62 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0096others(59): Show | 62 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.165+369C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111116060 | ||||||
| chr13:111116155
|
CTG | C | 126 | a0001c0001t0001g0160a0001c0001t0001g0167a0001c0001t0001g0168others(123): Show | 126 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.165+466_165+467del others(2): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111116155 | |||||
| chr13:111116205
|
C | T | 196 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0084others(193): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.165+514C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111116205 | ||||||
| chr13:111116242
|
A | G | 1 | a0001c0003t0003g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.165+551A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111116242 | ||||||
| chr13:111116299
|
G | GT | 134 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0084others(131): Show | 134 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.165+610dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111116299 | |||||
| chr13:111116495
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0039others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.165+804T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111116495 | ||||||
| chr13:111116708
|
GACA | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0007g0004others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+1023_165+1025d others(5): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111116708 | |||||
| chr13:111116951
|
C | T | 7 | a0001c0001t0003g0262a0001c0001t0003g0264a0001c0001t0003g0266others(4): Show | 7 | HG01123.hp1 HG01346.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+1260C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111116951 | ||||||
| chr13:111117005
|
G | A | 86 | a0001c0001t0001g0160a0001c0001t0001g0167a0001c0001t0001g0168others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.165+1314G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111117005 | ||||||
| chr13:111117107
|
G | C | 1 | a0001c0001t0012g0001 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.165+1416G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111117107 | ||||||
| chr13:111117182
|
C | T | 1 | a0001c0001t0006g0268 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.165+1491C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111117182 | ||||||
| chr13:111117286
|
A | G | 2 | a0001c0001t0011g0006a0001c0001t0011g0007 | 2 | HG01884.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.165+1595A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111117286 | ||||||
| chr13:111117336
|
A | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0007g0004others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+1645A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111117336 | ||||||
| chr13:111117411
|
C | T | 86 | a0001c0001t0001g0160a0001c0001t0001g0167a0001c0001t0001g0168others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.165+1720C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111117411 | ||||||
| chr13:111117423
|
T | C | 86 | a0001c0001t0001g0160a0001c0001t0001g0167a0001c0001t0001g0168others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.165+1732T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111117423 | ||||||
| chr13:111117688
|
T | C | 3 | a0001c0002t0002g0147a0001c0002t0002g0148a0001c0002t0002g0149 | 3 | HG01175.hp1 HG01361.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.165+1997T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111117688 | ||||||
| chr13:111117697
|
C | T | 1 | a0001c0001t0003g0145 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.165+2006C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111117697 | ||||||
| chr13:111117727
|
C | G | 1 | a0001c0002t0002g0221 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.165+2036C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111117727 | ||||||
| chr13:111117727
|
CTCCT | C | 17 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0002g0078others(14): Show | 17 | HG02280.hp1 HG02280.hp2 HG02647.hp2 others(14): Show |
intron_variant | MODIFIER | c.165+2051_165+2054d others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111117727 | |||||
| chr13:111117813
|
A | C | 86 | a0001c0001t0001g0160a0001c0001t0001g0167a0001c0001t0001g0168others(83): Show | 86 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.165+2122A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111117813 | ||||||
| chr13:111117853
|
C | T | 6 | a0001c0001t0002g0078a0001c0001t0006g0083a0001c0002t0002g0079others(3): Show | 6 | NA18939.hp1 NA18999.hp2 NA19063.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+2162C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111117853 | ||||||
| chr13:111117867
|
T | C | 1 | a0001c0002t0002g0150 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.165+2176T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111117867 | ||||||
| chr13:111117919
|
A | T | 9 | a0001c0001t0001g0074a0001c0001t0008g0073a0001c0001t0011g0070others(6): Show | 9 | HG02280.hp2 HG02647.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+2228A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111117919 | ||||||
| chr13:111118075
|
G | A | 9 | a0001c0001t0001g0074a0001c0001t0008g0073a0001c0001t0011g0070others(6): Show | 9 | HG02280.hp2 HG02647.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+2384G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111118075 | ||||||
| chr13:111118245
|
C | G | 9 | a0001c0001t0001g0074a0001c0001t0008g0073a0001c0001t0011g0070others(6): Show | 9 | HG02280.hp2 HG02647.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+2554C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111118245 | ||||||
| chr13:111118399
|
A | C | 8 | a0001c0001t0001g0068a0001c0001t0002g0078a0001c0001t0006g0083others(5): Show | 8 | HG02280.hp1 HG03486.hp1 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+2708A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111118399 | ||||||
| chr13:111118454
|
C | T | 3 | a0001c0001t0001g0144a0001c0001t0016g0143a0001c0003t0001g0142 | 3 | HG02886.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.165+2763C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111118454 | ||||||
| chr13:111118478
|
T | A | 1 | a0001c0001t0003g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.165+2787T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111118478 | ||||||
| chr13:111118490
|
G | T | 5 | a0001c0001t0001g0066a0001c0001t0001g0084a0001c0001t0004g0064others(2): Show | 5 | HG01884.hp2 HG02615.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+2799G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111118490 | ||||||
| chr13:111118515
|
C | G | 40 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0001g0232others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.165+2824C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111118515 | ||||||
| chr13:111118598
|
A | T | 2 | a0001c0001t0001g0027a0001c0001t0007g0028 | 2 | HG02572.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.165+2907A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111118598 | ||||||
| chr13:111118609
|
T | A | 25 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0043others(22): Show | 25 | HG00639.hp1 HG01109.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.165+2918T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111118609 | ||||||
| chr13:111118654
|
A | G | 150 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0096others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.165+2963A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111118654 | ||||||
| chr13:111118814
|
C | T | 1 | a0001c0001t0004g0261 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.165+3123C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111118814 | ||||||
| chr13:111118837
|
G | T | 63 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0096others(60): Show | 63 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.165+3146G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111118837 | ||||||
| chr13:111118909
|
G | T | 6 | a0001c0001t0002g0078a0001c0001t0006g0083a0001c0002t0002g0079others(3): Show | 6 | NA18939.hp1 NA18999.hp2 NA19063.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+3218G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111118909 | ||||||
| chr13:111118924
|
G | C | 2 | a0001c0001t0026g0053a0001c0007t0027g0054 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.165+3233G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111118924 | ||||||
| chr13:111118953
|
C | T | 6 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0007g0004others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+3262C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111118953 | ||||||
| chr13:111119024
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0039others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.165+3333T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111119024 | ||||||
| chr13:111119197
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.165+3506C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111119197 | ||||||
| chr13:111119263
|
A | G | 150 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0096others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.165+3572A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111119263 | ||||||
| chr13:111119303
|
G | T | 1 | a0001c0001t0003g0274 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.165+3612G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111119303 | ||||||
| chr13:111119326
|
G | A | 1 | a0001c0001t0004g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.165+3635G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111119326 | ||||||
| chr13:111119382
|
G | A | 87 | a0001c0001t0001g0160a0001c0001t0001g0167a0001c0001t0001g0168others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.165+3691G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111119382 | ||||||
| chr13:111119530
|
G | A | 9 | a0001c0001t0001g0074a0001c0001t0008g0073a0001c0001t0011g0070others(6): Show | 9 | HG02280.hp2 HG02647.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+3839G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111119530 | ||||||
| chr13:111119673
|
T | C | 87 | a0001c0001t0001g0160a0001c0001t0001g0167a0001c0001t0001g0168others(84): Show | 87 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.165+3982T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111119673 | ||||||
| chr13:111119872
|
C | T | 20 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0044others(17): Show | 20 | HG00639.hp1 HG01109.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.165+4181C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111119872 | ||||||
| chr13:111119991
|
C | T | 5 | a0001c0001t0005g0062a0001c0001t0034g0061a0001c0002t0002g0060others(2): Show | 5 | HG01167.hp2 HG01192.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+4300C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111119991 | ||||||
| chr13:111120045
|
G | A | 6 | a0001c0001t0002g0091a0001c0001t0003g0085a0001c0001t0003g0087others(3): Show | 6 | HG02015.hp2 HG02622.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+4354G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120045 | ||||||
| chr13:111120067
|
T | C | 36 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0096others(33): Show | 36 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.165+4376T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120067 | ||||||
| chr13:111120204
|
G | A | 25 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0043others(22): Show | 25 | HG00639.hp1 HG01109.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.165+4513G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120204 | ||||||
| chr13:111120218
|
C | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0039others(49): Show | 52 | HG00639.hp1 HG01109.hp2 HG01167.hp2 others(49): Show |
intron_variant | MODIFIER | c.165+4527C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120218 | ||||||
| chr13:111120231
|
A | G | 25 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0043others(22): Show | 25 | HG00639.hp1 HG01109.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.165+4540A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120231 | ||||||
| chr13:111120242
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.165+4551A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120242 | ||||||
| chr13:111120242
|
A | T | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.165+4551A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120242 | ||||||
| chr13:111120343
|
G | A | 25 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0043others(22): Show | 25 | HG00639.hp1 HG01109.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.165+4652G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120343 | ||||||
| chr13:111120406
|
C | T | 1 | a0001c0001t0032g0030 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.165+4715C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120406 | ||||||
| chr13:111120423
|
G | A | 67 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0066others(64): Show | 67 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.165+4732G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120423 | ||||||
| chr13:111120438
|
C | A | 6 | a0001c0001t0001g0039a0001c0001t0007g0034a0001c0001t0008g0035others(3): Show | 6 | HG02109.hp1 HG02559.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+4747C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120438 | ||||||
| chr13:111120472
|
T | C | 2 | a0001c0001t0001g0068a0002c0009t0002g0069 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.165+4781T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120472 | ||||||
| chr13:111120472
|
T | TAC | 118 | a0001c0001t0001g0066a0001c0001t0001g0074a0001c0001t0001g0084others(115): Show | 118 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.165+4793_165+4794d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111120472 | |||||
| chr13:111120472
|
T | TACAC | 5 | a0001c0001t0004g0222a0001c0001t0004g0223a0001c0001t0004g0224others(2): Show | 5 | HG01261.hp2 HG02109.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+4791_165+4794d others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111120472 | |||||
| chr13:111120472
|
TAC | T | 29 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0043others(26): Show | 29 | HG00639.hp1 HG00738.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.165+4793_165+4794d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111120472 | |||||
| chr13:111120502
|
T | C | 6 | a0001c0001t0002g0078a0001c0001t0006g0083a0001c0002t0002g0079others(3): Show | 6 | NA18939.hp1 NA18999.hp2 NA19063.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+4811T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120502 | ||||||
| chr13:111120504
|
GACACGCA others(1): Show |
G | 40 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0001g0232others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.165+4826_165+4833d others(10): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111120504 | |||||
| chr13:111120516
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.165+4825C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120516 | ||||||
| chr13:111120663
|
T | C | 2 | a0001c0001t0001g0040a0001c0001t0006g0041 | 2 | NA18952.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.165+4972T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120663 | ||||||
| chr13:111120761
|
A | G | 40 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0001g0232others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.165+5070A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120761 | ||||||
| chr13:111120786
|
C | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0066others(24): Show | 27 | HG01167.hp2 HG01192.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.165+5095C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120786 | ||||||
| chr13:111120880
|
G | A | 1 | a0004c0017t0003g0120 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165+5189G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120880 | ||||||
| chr13:111120969
|
C | G | 166 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0039others(163): Show | 166 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.165+5278C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111120969 | ||||||
| chr13:111121072
|
C | G | 253 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0039others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.165+5381C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111121072 | ||||||
| chr13:111121182
|
A | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0039others(60): Show | 63 | HG00639.hp1 HG01109.hp2 HG01167.hp2 others(60): Show |
intron_variant | MODIFIER | c.165+5491A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111121182 | ||||||
| chr13:111121214
|
C | T | 3 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260 | 3 | NA19000.hp1 NA19005.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.165+5523C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111121214 | ||||||
| chr13:111121329
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0039others(250): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.165+5638T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111121329 | ||||||
| chr13:111121431
|
T | C | 9 | a0001c0001t0001g0074a0001c0001t0008g0073a0001c0001t0011g0070others(6): Show | 9 | HG02280.hp2 HG02647.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+5740T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111121431 | ||||||
| chr13:111121467
|
T | G | 1 | a0001c0016t0008g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.165+5776T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111121467 | ||||||
| chr13:111121491
|
G | A | 2 | a0001c0002t0002g0151a0001c0002t0002g0152 | 2 | NA18941.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.165+5800G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111121491 | ||||||
| chr13:111121665
|
C | T | 2 | a0001c0002t0002g0148a0001c0002t0002g0149 | 2 | HG01361.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.165+5974C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111121665 | ||||||
| chr13:111121783
|
A | G | 6 | a0001c0001t0001g0056a0001c0001t0001g0084a0001c0001t0007g0057others(3): Show | 6 | HG01243.hp2 HG02055.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+6092A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111121783 | ||||||
| chr13:111121800
|
C | G | 50 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0039others(47): Show | 50 | HG00639.hp1 HG01109.hp2 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.165+6109C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111121800 | ||||||
| chr13:111121810
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.165+6119C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111121810 | ||||||
| chr13:111121910
|
A | T | 1 | a0001c0001t0006g0218 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.165+6219A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111121910 | ||||||
| chr13:111121941
|
G | A | 50 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0039others(47): Show | 50 | HG00639.hp1 HG01109.hp2 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.165+6250G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111121941 | ||||||
| chr13:111121995
|
A | G | 2 | a0001c0001t0001g0068a0002c0009t0002g0069 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.165+6304A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111121995 | ||||||
| chr13:111122208
|
A | G | 6 | a0001c0001t0001g0039a0001c0001t0007g0034a0001c0001t0008g0035others(3): Show | 6 | HG02109.hp1 HG02559.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+6517A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111122208 | ||||||
| chr13:111122521
|
T | C | 240 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.165+6830T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111122521 | ||||||
| chr13:111122657
|
C | T | 2 | a0001c0001t0001g0068a0002c0009t0002g0069 | 2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.165+6966C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111122657 | ||||||
| chr13:111122682
|
A | G | 2 | a0001c0001t0011g0076a0001c0001t0016g0077 | 2 | HG02280.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.165+6991A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111122682 | ||||||
| chr13:111122723
|
A | G | 1 | a0001c0001t0007g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.165+7032A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111122723 | ||||||
| chr13:111122820
|
C | T | 25 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0043others(22): Show | 25 | HG00639.hp1 HG01109.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.165+7129C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111122820 | ||||||
| chr13:111122821
|
G | A | 1 | a0001c0001t0003g0087 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.165+7130G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111122821 | ||||||
| chr13:111123050
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.165+7359T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111123050 | ||||||
| chr13:111123191
|
C | A | 2 | a0001c0001t0013g0154a0001c0001t0014g0153 | 2 | HG01943.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.165+7500C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111123191 | ||||||
| chr13:111123192
|
C | G | 1 | a0001c0001t0007g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.165+7501C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111123192 | ||||||
| chr13:111123278
|
T | A | 1 | a0001c0002t0002g0155 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.165+7587T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111123278 | ||||||
| chr13:111123295
|
A | G | 4 | a0001c0001t0001g0066a0001c0001t0004g0064a0001c0001t0004g0065others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+7604A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111123295 | ||||||
| chr13:111123344
|
C | A | 1 | a0001c0001t0005g0139 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.165+7653C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111123344 | ||||||
| chr13:111123397
|
A | G | 6 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0008g0003others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+7706A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111123397 | ||||||
| chr13:111123481
|
T | TCA | 40 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0001g0232others(37): Show | 40 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.165+7803_165+7804d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111123481 | |||||
| chr13:111123492
|
CACAT | C | 9 | a0001c0001t0001g0074a0001c0001t0008g0073a0001c0001t0011g0070others(6): Show | 9 | HG02280.hp2 HG02647.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+7806_165+7809d others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111123492 | |||||
| chr13:111123494
|
CAT | C | 24 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0056others(21): Show | 24 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.165+7805_165+7806d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111123494 | |||||
| chr13:111123496
|
T | C | 240 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0018others(237): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.165+7805T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111123496 | ||||||
| chr13:111123681
|
T | G | 6 | a0001c0001t0002g0078a0001c0001t0006g0083a0001c0002t0002g0079others(3): Show | 6 | NA18939.hp1 NA18999.hp2 NA19063.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+7990T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111123681 | ||||||
| chr13:111123772
|
G | A | 4 | a0001c0001t0001g0066a0001c0001t0004g0064a0001c0001t0004g0065others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+8081G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111123772 | ||||||
| chr13:111123848
|
G | A | 41 | a0001c0001t0001g0092a0001c0001t0001g0229a0001c0001t0001g0231others(38): Show | 41 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.165+8157G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111123848 | ||||||
| chr13:111123862
|
G | GC | 52 | a0001c0001t0001g0066a0001c0001t0001g0084a0001c0001t0001g0180others(49): Show | 52 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.165+8183dupC | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111123862 | |||||
| chr13:111123862
|
G | GCC | 39 | a0001c0001t0001g0093a0001c0001t0001g0096a0001c0001t0001g0097others(36): Show | 39 | HG00140.hp2 HG00597.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.165+8182_165+8183d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111123862 | |||||
| chr13:111123862
|
GC | G | 13 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0002g0078others(10): Show | 13 | HG01884.hp1 HG01981.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.165+8183delC | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111123862 | |||||
| chr13:111123862
|
GCC | G | 34 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0044others(31): Show | 34 | HG00639.hp1 HG01109.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.165+8182_165+8183d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111123862 | |||||
| chr13:111123862
|
GCCC | G | 77 | a0001c0001t0001g0027a0001c0001t0001g0043a0001c0001t0001g0074others(74): Show | 77 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.165+8181_165+8183d others(5): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111123862 | |||||
| chr13:111123867
|
C | G | 31 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0044others(28): Show | 31 | HG00639.hp1 HG01109.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.165+8176C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111123867 | ||||||
| chr13:111123880
|
C | T | 1 | a0001c0001t0006g0041 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.165+8189C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111123880 | ||||||
| chr13:111123920
|
T | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0008g0003others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+8229T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111123920 | ||||||
| chr13:111124018
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.165+8327T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111124018 | ||||||
| chr13:111124208
|
T | A | 3 | a0001c0001t0002g0156a0001c0004t0022g0208a0001c0004t0022g0209 | 3 | NA18939.hp2 NA19056.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.165+8517T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111124208 | ||||||
| chr13:111124299
|
G | T | 3 | a0001c0001t0001g0056a0001c0001t0007g0057a0001c0001t0011g0055 | 3 | HG01243.hp2 HG02055.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.165+8608G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111124299 | ||||||
| chr13:111124354
|
C | T | 31 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0043others(28): Show | 31 | HG00639.hp1 HG01109.hp2 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.165+8663C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111124354 | ||||||
| chr13:111124569
|
C | T | 1 | a0001c0001t0003g0274 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.165+8878C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111124569 | ||||||
| chr13:111124670
|
C | G | 1 | a0001c0001t0007g0008 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.165+8979C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111124670 | ||||||
| chr13:111124671
|
C | T | 1 | a0001c0001t0007g0008 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.165+8980C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111124671 | ||||||
| chr13:111124683
|
G | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.165+8992G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111124683 | ||||||
| chr13:111124704
|
C | T | 1 | a0001c0001t0015g0273 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.165+9013C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111124704 | ||||||
| chr13:111124757
|
TTTTTGTT others(3): Show |
T | 6 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0004g0064others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+9076_165+9085d others(12): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111124757 | |||||
| chr13:111124902
|
G | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0217 | 2 | HG01109.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.165+9211G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111124902 | ||||||
| chr13:111124951
|
G | T | 6 | a0001c0001t0002g0078a0001c0001t0006g0083a0001c0002t0002g0079others(3): Show | 6 | NA18939.hp1 NA18999.hp2 NA19063.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+9260G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111124951 | ||||||
| chr13:111125385
|
C | CT | 171 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.165+9707dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111125385 | |||||
| chr13:111125487
|
C | A | 1 | a0001c0001t0005g0139 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.165+9796C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111125487 | ||||||
| chr13:111125666
|
C | T | 211 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0027others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.165+9975C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111125666 | ||||||
| chr13:111125766
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0008g0003others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+10075G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111125766 | ||||||
| chr13:111125832
|
C | A | 4 | a0001c0001t0001g0066a0001c0001t0004g0064a0001c0001t0004g0065others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+10141C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111125832 | ||||||
| chr13:111125899
|
A | G | 1 | a0001c0001t0004g0254 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.165+10208A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111125899 | ||||||
| chr13:111125941
|
G | T | 1 | a0001c0001t0007g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.165+10250G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111125941 | ||||||
| chr13:111125991
|
G | C | 24 | a0001c0001t0001g0027a0001c0001t0001g0125a0001c0001t0001g0129others(21): Show | 24 | HG00741.hp2 HG01175.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.165+10300G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111125991 | ||||||
| chr13:111126011
|
G | C | 1 | a0004c0017t0003g0120 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.165+10320G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111126011 | ||||||
| chr13:111126038
|
T | C | 9 | a0001c0001t0001g0074a0001c0001t0008g0073a0001c0001t0011g0070others(6): Show | 9 | HG02280.hp2 HG02647.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+10347T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111126038 | ||||||
| chr13:111126163
|
T | C | 1 | a0001c0001t0017g0269 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.165+10472T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111126163 | ||||||
| chr13:111126218
|
C | A | 1 | a0001c0001t0003g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.165+10527C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111126218 | ||||||
| chr13:111126269
|
T | C | 6 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0008g0003others(3): Show | 6 | HG01884.hp1 HG02258.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+10578T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111126269 | ||||||
| chr13:111126359
|
G | A | 2 | a0001c0001t0001g0180a0001c0013t0001g0100 | 2 | HG00642.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.165+10668G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111126359 | ||||||
| chr13:111126383
|
G | C | 1 | a0001c0001t0016g0012 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.165+10692G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111126383 | ||||||
| chr13:111126489
|
CA | C | 8 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0004g0064others(5): Show | 8 | HG01884.hp2 HG02280.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.165+10813delA | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111126489 | |||||
| chr13:111126648
|
G | T | 1 | a0001c0001t0001g0207 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.165+10957G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111126648 | ||||||
| chr13:111126775
|
A | G | 1 | a0001c0002t0002g0060 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.165+11084A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111126775 | ||||||
| chr13:111126931
|
T | C | 149 | a0001c0001t0001g0027a0001c0001t0001g0092a0001c0001t0001g0093others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.165+11240T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111126931 | ||||||
| chr13:111127039
|
A | G | 2 | a0001c0001t0026g0053a0001c0007t0027g0054 | 2 | NA19240.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.165+11348A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111127039 | ||||||
| chr13:111127061
|
CAG | C | 6 | a0001c0001t0002g0078a0001c0001t0006g0083a0001c0002t0002g0079others(3): Show | 6 | NA18939.hp1 NA18999.hp2 NA19063.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+11372_165+1137 others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111127061 | |||||
| chr13:111127074
|
C | T | 7 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0003g0179others(4): Show | 7 | HG01884.hp1 HG02258.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+11383C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111127074 | ||||||
| chr13:111127263
|
A | G | 1 | a0001c0002t0002g0155 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.165+11572A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111127263 | ||||||
| chr13:111127339
|
T | A | 16 | a0001c0001t0001g0093a0001c0001t0001g0113a0001c0001t0002g0091others(13): Show | 16 | HG00738.hp1 HG01081.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.165+11648T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111127339 | ||||||
| chr13:111127385
|
G | A | 88 | a0001c0001t0001g0123a0001c0001t0001g0160a0001c0001t0001g0167others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.165+11694G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111127385 | ||||||
| chr13:111127426
|
G | C | 1 | a0001c0001t0007g0008 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.165+11735G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111127426 | ||||||
| chr13:111127484
|
C | G | 60 | a0001c0001t0001g0027a0001c0001t0001g0092a0001c0001t0001g0093others(57): Show | 60 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.165+11793C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111127484 | ||||||
| chr13:111127648
|
G | GA | 22 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0229others(19): Show | 22 | HG01516.hp1 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.165+11982dupA | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111127648 | |||||
| chr13:111127648
|
G | GAA | 6 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0018others(3): Show | 6 | HG01109.hp1 HG02818.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+11981_165+1198 others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111127648 | |||||
| chr13:111127648
|
GA | G | 10 | a0001c0001t0001g0039a0001c0001t0001g0253a0001c0001t0003g0024others(7): Show | 10 | HG00323.hp2 HG01257.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+11982delA | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111127648 | |||||
| chr13:111127669
|
AAAAAG | A | 31 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0096others(28): Show | 31 | HG00140.hp2 HG00280.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.165+11981_165+1198 others(9): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111127669 | |||||
| chr13:111127773
|
T | C | 3 | a0001c0001t0001g0056a0001c0001t0007g0057a0001c0001t0011g0055 | 3 | HG01243.hp2 HG02055.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.165+12082T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111127773 | ||||||
| chr13:111127878
|
C | T | 6 | a0001c0001t0002g0078a0001c0001t0006g0083a0001c0002t0002g0079others(3): Show | 6 | NA18939.hp1 NA18999.hp2 NA19063.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+12187C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111127878 | ||||||
| chr13:111127927
|
A | G | 1 | a0001c0001t0004g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.165+12236A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111127927 | ||||||
| chr13:111128149
|
C | A | 1 | a0001c0002t0002g0158 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.165+12458C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111128149 | ||||||
| chr13:111128161
|
G | A | 1 | a0001c0001t0017g0269 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.165+12470G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111128161 | ||||||
| chr13:111128250
|
G | C | 60 | a0001c0001t0001g0027a0001c0001t0001g0092a0001c0001t0001g0093others(57): Show | 60 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.165+12559G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111128250 | ||||||
| chr13:111128303
|
AATTGT | A | 5 | a0001c0001t0005g0062a0001c0001t0034g0061a0001c0002t0002g0060others(2): Show | 5 | HG01167.hp2 HG01192.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+12615_165+1261 others(9): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111128303 | |||||
| chr13:111128499
|
G | GCAAA | 6 | a0001c0001t0001g0056a0001c0001t0003g0178a0001c0001t0003g0216others(3): Show | 6 | HG00140.hp1 HG01099.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.165+12833_165+1283 others(8): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111128499 | |||||
| chr13:111128713
|
C | G | 48 | a0001c0001t0001g0074a0001c0001t0001g0229a0001c0001t0001g0231others(45): Show | 48 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.165+13022C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111128713 | ||||||
| chr13:111129001
|
T | C | 1 | a0001c0002t0001g0182 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.165+13310T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111129001 | ||||||
| chr13:111129196
|
T | C | 12 | a0001c0001t0002g0078a0001c0001t0006g0083a0001c0001t0009g0258others(9): Show | 12 | NA18939.hp1 NA18957.hp1 NA18966.hp1 others(9): Show |
intron_variant | MODIFIER | c.165+13505T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111129196 | ||||||
| chr13:111129374
|
A | T | 35 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0001g0232others(32): Show | 35 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.165+13683A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111129374 | ||||||
| chr13:111129521
|
A | G | 1 | a0001c0001t0001g0018 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.165+13830A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111129521 | ||||||
| chr13:111129604
|
T | C | 1 | a0001c0002t0002g0206 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.165+13913T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111129604 | ||||||
| chr13:111129687
|
C | T | 1 | a0001c0001t0003g0215 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.165+13996C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111129687 | ||||||
| chr13:111129759
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.165+14068C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111129759 | ||||||
| chr13:111130034
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.165+14343C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111130034 | ||||||
| chr13:111130193
|
G | T | 2 | a0001c0008t0001g0098a0001c0008t0001g0109 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.165+14502G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111130193 | ||||||
| chr13:111130304
|
T | C | 4 | a0001c0001t0001g0068a0001c0001t0012g0001a0001c0001t0026g0053others(1): Show | 4 | HG02280.hp1 HG03471.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+14613T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111130304 | ||||||
| chr13:111130389
|
A | G | 1 | a0001c0001t0003g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.165+14698A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111130389 | ||||||
| chr13:111130461
|
G | A | 1 | a0001c0002t0002g0221 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.165+14770G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111130461 | ||||||
| chr13:111130530
|
A | T | 44 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0001g0092others(41): Show | 44 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.165+14839A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111130530 | ||||||
| chr13:111130743
|
C | T | 1 | a0006c0019t0002g0175 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.165+15052C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111130743 | ||||||
| chr13:111130789
|
G | A | 2 | a0001c0001t0001g0019a0001c0007t0004g0059 | 2 | HG03139.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.165+15098G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111130789 | ||||||
| chr13:111130879
|
C | G | 268 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.165+15188C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111130879 | ||||||
| chr13:111131028
|
C | T | 202 | a0001c0001t0001g0016a0001c0001t0001g0040a0001c0001t0001g0043others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.165+15337C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111131028 | ||||||
| chr13:111131107
|
A | G | 47 | a0001c0001t0001g0005a0001c0001t0001g0125a0001c0001t0001g0129others(44): Show | 47 | HG00642.hp1 HG00741.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.165+15416A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111131107 | ||||||
| chr13:111131216
|
C | T | 1 | a0001c0002t0002g0174 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.165+15525C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111131216 | ||||||
| chr13:111131258
|
G | A | 5 | a0001c0001t0003g0252a0001c0002t0002g0257a0001c0002t0021g0255others(2): Show | 5 | NA18957.hp1 NA18966.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+15567G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111131258 | ||||||
| chr13:111131273
|
G | C | 2 | a0001c0001t0004g0110a0001c0001t0017g0270 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.165+15582G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111131273 | ||||||
| chr13:111131299
|
T | C | 1 | a0002c0009t0002g0069 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.165+15608T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111131299 | ||||||
| chr13:111131339
|
C | T | 89 | a0001c0001t0001g0040a0001c0001t0001g0047a0001c0001t0001g0048others(86): Show | 89 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.165+15648C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111131339 | ||||||
| chr13:111131704
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0188 | 2 | HG01109.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.165+16013T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111131704 | ||||||
| chr13:111132001
|
G | C | 2 | a0001c0001t0005g0230a0002c0009t0002g0069 | 2 | HG01071.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.165+16310G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111132001 | ||||||
| chr13:111132110
|
C | T | 1 | a0001c0001t0015g0273 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.165+16419C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111132110 | ||||||
| chr13:111132211
|
G | A | 58 | a0001c0001t0001g0084a0001c0001t0001g0092a0001c0001t0001g0097others(55): Show | 58 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.165+16520G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111132211 | ||||||
| chr13:111132477
|
A | G | 1 | a0001c0006t0012g0124 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.165+16786A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111132477 | ||||||
| chr13:111132557
|
A | G | 1 | a0001c0001t0005g0115 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.165+16866A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111132557 | ||||||
| chr13:111132633
|
T | C | 1 | a0001c0002t0010g0163 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.165+16942T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111132633 | ||||||
| chr13:111132727
|
G | C | 4 | a0001c0002t0002g0257a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18957.hp1 NA18966.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+17036G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111132727 | ||||||
| chr13:111133049
|
CAT | C | 7 | a0001c0001t0001g0074a0001c0001t0001g0096a0001c0001t0011g0006others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.165+17361_165+1736 others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133049 | |||||
| chr13:111133112
|
T | C | 4 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260others(1): Show | 4 | NA19000.hp1 NA19005.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+17421T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111133112 | ||||||
| chr13:111133285
|
C | T | 1 | a0001c0001t0002g0251 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.165+17594C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111133285 | ||||||
| chr13:111133291
|
T | C | 1 | a0001c0002t0006g0236 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.165+17600T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111133291 | ||||||
| chr13:111133484
|
T | A | 4 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260others(1): Show | 4 | NA19000.hp1 NA19005.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.165+17793T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111133484 | ||||||
| chr13:111133658
|
G | T | 59 | a0001c0001t0001g0084a0001c0001t0001g0092a0001c0001t0001g0097others(56): Show | 59 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.165+17967G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111133658 | ||||||
| chr13:111133757
|
TTTTCTTT others(5): Show |
T | 1 | a0001c0001t0001g0113 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.165+18068_165+1807 others(16): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133757 | |||||
| chr13:111133763
|
T | A | 1 | a0001c0001t0001g0044 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.165+18072T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111133763 | ||||||
| chr13:111133763
|
T | TATATATA others(4): Show |
1 | a0001c0001t0001g0123 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.165+18072_165+1807 others(15): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111133763 | ||||||
| chr13:111133763
|
TTA | T | 11 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0052others(8): Show | 11 | HG01516.hp2 HG01993.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.165+18122_165+1812 others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133763 | |||||
| chr13:111133763
|
TTATA | T | 12 | a0001c0001t0001g0019a0001c0001t0001g0027a0001c0001t0001g0056others(9): Show | 12 | HG01243.hp2 HG02572.hp2 HG03130.hp2 others(9): Show |
intron_variant | MODIFIER | c.165+18120_165+1812 others(8): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133763 | |||||
| chr13:111133763
|
TTATATA | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0048others(11): Show | 14 | HG00639.hp1 HG01192.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.165+18118_165+1812 others(10): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133763 | |||||
| chr13:111133763
|
TTATATAT others(1): Show |
T | 9 | a0001c0001t0001g0018a0001c0001t0003g0025a0001c0001t0004g0122others(6): Show | 9 | HG01192.hp1 HG02970.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.165+18116_165+1812 others(12): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133763 | |||||
| chr13:111133763
|
TTATATAT others(3): Show |
T | 4 | a0001c0001t0001g0105a0001c0001t0003g0210a0001c0001t0003g0228others(1): Show | 4 | HG00280.hp1 HG02055.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+18114_165+1812 others(14): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133763 | |||||
| chr13:111133763
|
TTATATAT others(5): Show |
T | 1 | a0001c0016t0008g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.165+18112_165+1812 others(16): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133763 | |||||
| chr13:111133763
|
TTATATAT others(7): Show |
T | 29 | a0001c0001t0001g0016a0001c0001t0001g0066a0001c0001t0001g0129others(26): Show | 29 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.165+18110_165+1812 others(18): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133763 | |||||
| chr13:111133763
|
TTATATAT others(9): Show |
T | 31 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0144others(28): Show | 31 | HG00099.hp2 HG00140.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.165+18108_165+1812 others(20): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133763 | |||||
| chr13:111133763
|
TTATATAT others(11): Show |
T | 15 | a0001c0001t0001g0047a0001c0001t0001g0074a0001c0001t0003g0089others(12): Show | 15 | HG00642.hp1 HG01069.hp2 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.165+18106_165+1812 others(22): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133763 | |||||
| chr13:111133763
|
TTATATAT others(13): Show |
T | 33 | a0001c0001t0001g0005a0001c0001t0001g0096a0001c0001t0001g0160others(30): Show | 33 | HG01243.hp1 HG01257.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.165+18104_165+1812 others(24): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133763 | |||||
| chr13:111133763
|
TTATATAT others(19): Show |
T | 2 | a0001c0001t0002g0078a0001c0006t0012g0121 | 2 | HG00741.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.165+18098_165+1812 others(30): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133763 | |||||
| chr13:111133763
|
TTATATAT others(21): Show |
T | 2 | a0001c0001t0001g0093a0001c0001t0008g0015 | 2 | HG02818.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.165+18096_165+1812 others(32): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133763 | |||||
| chr13:111133763
|
TTATATAT others(23): Show |
T | 12 | a0001c0001t0001g0039a0001c0001t0001g0068a0001c0001t0002g0164others(9): Show | 12 | HG02015.hp1 HG02132.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.165+18094_165+1812 others(34): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133763 | |||||
| chr13:111133763
|
TTATATAT others(25): Show |
T | 4 | a0001c0001t0001g0125a0001c0001t0005g0230a0001c0001t0007g0057others(1): Show | 4 | HG00741.hp2 HG01071.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+18092_165+1812 others(36): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133763 | |||||
| chr13:111133764
|
T | C | 1 | a0001c0001t0033g0101 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.165+18073T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111133764 | ||||||
| chr13:111133789
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.165+18098A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111133789 | ||||||
| chr13:111133805
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(5): Show | 8 | HG01243.hp2 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.165+18114A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111133805 | ||||||
| chr13:111133808
|
T | A | 54 | a0001c0001t0001g0074a0001c0001t0001g0084a0001c0001t0001g0092others(51): Show | 54 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.165+18117T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111133808 | ||||||
| chr13:111133808
|
T | TATAA | 4 | a0001c0001t0002g0011a0001c0001t0003g0107a0001c0001t0005g0062others(1): Show | 4 | HG02257.hp2 HG02572.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+18120_165+1812 others(8): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133808 | |||||
| chr13:111133812
|
T | A | 208 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(205): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.165+18121T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111133812 | ||||||
| chr13:111133812
|
T | TAA | 11 | a0001c0001t0001g0167a0001c0001t0001g0195a0001c0001t0001g0196others(8): Show | 11 | HG00558.hp2 HG01943.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.165+18122_165+1812 others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133812 | |||||
| chr13:111133812
|
T | TATAA | 19 | a0001c0001t0001g0051a0001c0001t0001g0106a0001c0001t0001g0168others(16): Show | 19 | HG00558.hp1 HG00597.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.165+18123_165+1812 others(8): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133812 | |||||
| chr13:111133812
|
T | TATATAA | 8 | a0001c0001t0001g0207a0001c0001t0003g0213a0001c0001t0005g0212others(5): Show | 8 | HG01175.hp1 HG02004.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.165+18123_165+1812 others(10): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133812 | |||||
| chr13:111133812
|
T | TATATAAA others(5): Show |
1 | a0001c0001t0001g0137 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.165+18123_165+1812 others(16): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133812 | |||||
| chr13:111133812
|
T | TATATAAA others(3): Show |
1 | a0001c0001t0008g0073 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.165+18123_165+1812 others(14): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133812 | |||||
| chr13:111133812
|
T | TATATATA others(1): Show |
7 | a0001c0001t0001g0219a0001c0001t0003g0266a0001c0001t0004g0133others(4): Show | 7 | HG00099.hp1 HG01516.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.165+18123_165+1812 others(12): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133812 | |||||
| chr13:111133812
|
T | TATATATA others(3): Show |
4 | a0001c0001t0003g0178a0001c0001t0009g0258a0001c0001t0009g0260others(1): Show | 4 | HG01099.hp1 NA19000.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.165+18123_165+1812 others(14): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133812 | |||||
| chr13:111133812
|
T | TATATATA others(5): Show |
1 | a0001c0002t0001g0182 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.165+18123_165+1812 others(16): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111133812 | |||||
| chr13:111133825
|
T | G | 1 | a0001c0002t0002g0148 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.165+18134T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111133825 | ||||||
| chr13:111133839
|
C | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(2): Show | 5 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+18148C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111133839 | ||||||
| chr13:111133929
|
T | A | 5 | a0001c0001t0003g0252a0001c0002t0002g0257a0001c0002t0021g0255others(2): Show | 5 | NA18957.hp1 NA18966.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+18238T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111133929 | ||||||
| chr13:111133931
|
T | C | 5 | a0001c0001t0001g0113a0001c0001t0003g0119a0001c0001t0005g0114others(2): Show | 5 | HG00738.hp1 HG01081.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+18240T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111133931 | ||||||
| chr13:111134015
|
A | G | 2 | a0001c0001t0003g0107a0001c0001t0003g0136 | 2 | HG01891.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.165+18324A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111134015 | ||||||
| chr13:111134016
|
T | C | 1 | a0001c0001t0017g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.165+18325T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111134016 | ||||||
| chr13:111134039
|
G | A | 3 | a0001c0001t0002g0099a0001c0001t0011g0055a0001c0007t0027g0054 | 3 | HG02055.hp1 HG03540.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.165+18348G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111134039 | ||||||
| chr13:111134047
|
G | C | 85 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0052others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.165+18356G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111134047 | ||||||
| chr13:111134297
|
G | T | 1 | a0001c0001t0029g0201 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.165+18606G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111134297 | ||||||
| chr13:111134378
|
A | T | 5 | a0001c0001t0001g0113a0001c0001t0003g0119a0001c0001t0005g0114others(2): Show | 5 | HG00738.hp1 HG01081.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.165+18687A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111134378 | ||||||
| chr13:111134637
|
GTTGT | G | 2 | a0001c0001t0005g0062a0007c0010t0001g0095 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.165+18953_165+1895 others(8): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111134637 | |||||
| chr13:111134721
|
A | C | 3 | a0001c0001t0005g0230a0001c0001t0007g0057a0002c0009t0002g0069 | 3 | HG01071.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.165+19030A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111134721 | ||||||
| chr13:111134746
|
C | G | 68 | a0001c0001t0001g0074a0001c0001t0001g0084a0001c0001t0001g0092others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.165+19055C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111134746 | ||||||
| chr13:111134888
|
T | A | 84 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0052others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.166-19017T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111134888 | ||||||
| chr13:111135281
|
G | A | 1 | a0001c0001t0003g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.166-18624G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111135281 | ||||||
| chr13:111135369
|
G | A | 1 | a0001c0001t0005g0212 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.166-18536G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111135369 | ||||||
| chr13:111135507
|
G | A | 45 | a0001c0001t0001g0005a0001c0001t0001g0125a0001c0001t0001g0129others(42): Show | 45 | HG00558.hp2 HG00642.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.166-18398G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111135507 | ||||||
| chr13:111135569
|
A | C | 4 | a0001c0001t0003g0107a0001c0001t0003g0136a0001c0001t0005g0062others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-18336A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111135569 | ||||||
| chr13:111135627
|
A | G | 1 | a0001c0001t0008g0073 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.166-18278A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111135627 | ||||||
| chr13:111135772
|
T | C | 1 | a0001c0001t0033g0101 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.166-18133T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111135772 | ||||||
| chr13:111135942
|
T | C | 1 | a0001c0002t0024g0183 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.166-17963T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111135942 | ||||||
| chr13:111136078
|
G | A | 5 | a0001c0001t0001g0113a0001c0001t0003g0119a0001c0001t0005g0114others(2): Show | 5 | HG00738.hp1 HG01081.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-17827G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111136078 | ||||||
| chr13:111136492
|
C | G | 2 | a0001c0001t0004g0110a0001c0001t0017g0270 | 2 | HG02622.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.166-17413C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111136492 | ||||||
| chr13:111136710
|
C | A | 2 | a0001c0001t0001g0019a0001c0007t0004g0059 | 2 | HG03139.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.166-17195C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111136710 | ||||||
| chr13:111136888
|
C | T | 1 | a0001c0001t0007g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.166-17017C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111136888 | ||||||
| chr13:111136972
|
C | T | 1 | a0002c0009t0002g0069 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.166-16933C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111136972 | ||||||
| chr13:111137074
|
A | G | 5 | a0001c0001t0003g0252a0001c0002t0002g0257a0001c0002t0021g0255others(2): Show | 5 | NA18957.hp1 NA18966.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-16831A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111137074 | ||||||
| chr13:111137216
|
A | T | 7 | a0001c0001t0001g0129a0001c0001t0007g0094a0001c0001t0008g0003others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-16689A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111137216 | ||||||
| chr13:111137248
|
G | T | 7 | a0001c0001t0001g0074a0001c0001t0001g0096a0001c0001t0011g0006others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-16657G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111137248 | ||||||
| chr13:111137396
|
A | G | 1 | a0001c0002t0002g0257 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.166-16509A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111137396 | ||||||
| chr13:111137910
|
G | A | 7 | a0001c0001t0001g0074a0001c0001t0001g0096a0001c0001t0011g0006others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-15995G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111137910 | ||||||
| chr13:111138199
|
G | C | 1 | a0001c0001t0008g0073 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.166-15706G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111138199 | ||||||
| chr13:111138337
|
C | T | 15 | a0001c0001t0001g0040a0001c0001t0001g0047a0001c0001t0001g0048others(12): Show | 15 | HG00639.hp1 HG01169.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.166-15568C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111138337 | ||||||
| chr13:111138538
|
C | T | 2 | a0001c0001t0012g0001a0001c0001t0026g0053 | 2 | HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.166-15367C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111138538 | ||||||
| chr13:111138760
|
T | C | 4 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260others(1): Show | 4 | NA19000.hp1 NA19005.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-15145T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111138760 | ||||||
| chr13:111139018
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.166-14887G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111139018 | ||||||
| chr13:111139256
|
G | A | 4 | a0001c0001t0002g0099a0001c0001t0008g0073a0001c0001t0011g0055others(1): Show | 4 | HG02055.hp1 HG03041.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-14649G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111139256 | ||||||
| chr13:111139318
|
C | T | 4 | a0001c0001t0001g0160a0001c0001t0003g0266a0001c0001t0006g0041others(1): Show | 4 | HG01978.hp2 NA18966.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-14587C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111139318 | ||||||
| chr13:111139443
|
A | G | 3 | a0001c0001t0005g0230a0001c0001t0017g0269a0002c0009t0002g0069 | 3 | HG01071.hp1 HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.166-14462A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111139443 | ||||||
| chr13:111139480
|
C | T | 7 | a0001c0001t0001g0074a0001c0001t0001g0096a0001c0001t0011g0006others(4): Show | 7 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-14425C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111139480 | ||||||
| chr13:111139539
|
T | TGGGTGCC others(16): Show |
15 | a0001c0001t0001g0040a0001c0001t0001g0047a0001c0001t0001g0048others(12): Show | 15 | HG00639.hp1 HG01169.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.166-14333_166-1431 others(27): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111139539 | |||||
| chr13:111139549
|
CGTGGAGC others(39): Show |
C | 4 | a0001c0002t0002g0257a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18957.hp1 NA18966.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-14317_166-1427 others(50): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111139549 | |||||
| chr13:111139572
|
CGTGGAGC others(16): Show |
C | 1 | a0001c0001t0003g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.166-14310_166-1428 others(27): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111139572 | |||||
| chr13:111139595
|
T | C | 1 | a0001c0001t0003g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.166-14310T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111139595 | ||||||
| chr13:111139627
|
C | G | 2 | a0001c0001t0004g0238a0001c0001t0004g0239 | 2 | HG02135.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.166-14278C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111139627 | ||||||
| chr13:111139835
|
G | A | 2 | a0001c0006t0012g0121a0001c0006t0012g0124 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.166-14070G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111139835 | ||||||
| chr13:111139868
|
C | T | 3 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260 | 3 | NA19000.hp1 NA19005.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.166-14037C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111139868 | ||||||
| chr13:111139902
|
A | G | 11 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(8): Show | 11 | HG01243.hp2 HG02451.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.166-14003A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111139902 | ||||||
| chr13:111139910
|
T | G | 264 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.166-13995T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111139910 | ||||||
| chr13:111139938
|
A | G | 1 | a0001c0001t0003g0088 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.166-13967A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111139938 | ||||||
| chr13:111139949
|
G | A | 68 | a0001c0001t0001g0074a0001c0001t0001g0084a0001c0001t0001g0092others(65): Show | 68 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.166-13956G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111139949 | ||||||
| chr13:111139993
|
G | A | 4 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260others(1): Show | 4 | NA19000.hp1 NA19005.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.166-13912G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111139993 | ||||||
| chr13:111140168
|
T | C | 2 | a0001c0001t0012g0001a0001c0001t0026g0053 | 2 | HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.166-13737T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111140168 | ||||||
| chr13:111140210
|
C | T | 42 | a0001c0001t0001g0005a0001c0001t0001g0125a0001c0001t0001g0129others(39): Show | 42 | HG00642.hp1 HG00741.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.166-13695C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111140210 | ||||||
| chr13:111140517
|
C | G | 5 | a0001c0001t0001g0113a0001c0001t0003g0119a0001c0001t0005g0114others(2): Show | 5 | HG00738.hp1 HG01081.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-13388C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111140517 | ||||||
| chr13:111140517
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.166-13388C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111140517 | ||||||
| chr13:111141154
|
T | G | 2 | a0001c0001t0001g0135a0001c0001t0005g0063 | 2 | HG01175.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.166-12751T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111141154 | ||||||
| chr13:111141165
|
A | G | 2 | a0001c0001t0004g0133a0001c0001t0004g0134 | 2 | NA19066.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.166-12740A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111141165 | ||||||
| chr13:111141327
|
T | G | 1 | a0001c0001t0001g0217 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.166-12578T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111141327 | ||||||
| chr13:111141347
|
A | C | 6 | a0001c0001t0009g0214a0001c0001t0009g0250a0001c0001t0009g0258others(3): Show | 6 | NA18982.hp1 NA19000.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-12558A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111141347 | ||||||
| chr13:111141349
|
C | T | 6 | a0001c0001t0009g0214a0001c0001t0009g0250a0001c0001t0009g0258others(3): Show | 6 | NA18982.hp1 NA19000.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.166-12556C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111141349 | ||||||
| chr13:111141358
|
G | GT | 36 | a0001c0001t0001g0016a0001c0001t0001g0066a0001c0001t0001g0074others(33): Show | 36 | HG00642.hp1 HG01069.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.166-12535dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111141358 | |||||
| chr13:111141358
|
GT | G | 34 | a0001c0001t0001g0005a0001c0001t0001g0084a0001c0001t0001g0129others(31): Show | 34 | HG00558.hp2 HG00741.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.166-12535delT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111141358 | |||||
| chr13:111141358
|
GTT | G | 5 | a0001c0001t0001g0039a0001c0001t0004g0064a0001c0001t0004g0065others(2): Show | 5 | HG02615.hp2 HG02647.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-12536_166-1253 others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111141358 | |||||
| chr13:111141442
|
T | TG | 9 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0093others(6): Show | 9 | HG01192.hp1 HG02258.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-12458dupG | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111141442 | |||||
| chr13:111141455
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.166-12450G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111141455 | ||||||
| chr13:111141476
|
T | G | 7 | a0001c0001t0001g0014a0001c0001t0003g0025a0001c0001t0004g0122others(4): Show | 7 | HG02258.hp2 HG02818.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-12429T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111141476 | ||||||
| chr13:111141517
|
T | C | 1 | a0001c0001t0019g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.166-12388T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111141517 | ||||||
| chr13:111141632
|
AT | A | 13 | a0001c0001t0001g0051a0001c0001t0003g0128a0001c0001t0005g0116others(10): Show | 13 | HG01169.hp1 HG01257.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.166-12261delT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111141632 | |||||
| chr13:111141774
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.166-12131G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111141774 | ||||||
| chr13:111142066
|
T | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0219 | 2 | HG00099.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.166-11839T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111142066 | ||||||
| chr13:111142386
|
G | GGAATTCT others(34): Show |
269 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.166-11516_166-1151 others(45): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111142386 | |||||
| chr13:111142386
|
G | GGAATTCT others(34): Show |
1 | a0001c0001t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.166-11516_166-1151 others(45): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111142386 | |||||
| chr13:111142406
|
G | T | 1 | a0001c0001t0002g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.166-11499G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111142406 | ||||||
| chr13:111142430
|
G | C | 1 | a0001c0002t0002g0204 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.166-11475G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111142430 | ||||||
| chr13:111142611
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0003g0107a0001c0001t0003g0136others(3): Show | 6 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.166-11294T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111142611 | ||||||
| chr13:111142779
|
T | C | 1 | a0001c0001t0003g0089 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.166-11126T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111142779 | ||||||
| chr13:111142799
|
T | C | 1 | a0001c0001t0003g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.166-11106T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111142799 | ||||||
| chr13:111142869
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.166-11036C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111142869 | ||||||
| chr13:111142939
|
CTT | C | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-10965_166-1096 others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111142939 | ||||||
| chr13:111143032
|
T | G | 170 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0016others(167): Show | 170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.166-10873T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111143032 | ||||||
| chr13:111143075
|
G | C | 100 | a0001c0001t0001g0005a0001c0001t0001g0092a0001c0001t0001g0097others(97): Show | 100 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.166-10830G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111143075 | ||||||
| chr13:111143197
|
C | T | 43 | a0001c0001t0001g0068a0001c0001t0001g0084a0001c0001t0002g0078others(40): Show | 43 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.166-10708C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111143197 | ||||||
| chr13:111143200
|
T | C | 2 | a0001c0001t0001g0173a0001c0001t0001g0205 | 2 | HG01952.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.166-10705T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111143200 | ||||||
| chr13:111143209
|
G | C | 2 | a0002c0009t0002g0069a0002c0009t0002g0112 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.166-10696G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111143209 | ||||||
| chr13:111143225
|
T | C | 23 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(20): Show | 23 | HG01081.hp1 HG01192.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.166-10680T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111143225 | ||||||
| chr13:111143357
|
G | A | 3 | a0001c0001t0003g0128a0001c0001t0005g0114a0001c0001t0005g0126 | 3 | HG01081.hp1 HG01952.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.166-10548G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111143357 | ||||||
| chr13:111143593
|
T | C | 1 | a0001c0001t0006g0234 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.166-10312T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111143593 | ||||||
| chr13:111143626
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.166-10279C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111143626 | ||||||
| chr13:111143826
|
G | A | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-10079G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111143826 | ||||||
| chr13:111143923
|
A | G | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.166-9982A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111143923 | ||||||
| chr13:111144047
|
A | T | 8 | a0001c0001t0003g0128a0001c0001t0005g0114a0001c0001t0005g0116others(5): Show | 8 | HG01081.hp1 HG01257.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-9858A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111144047 | ||||||
| chr13:111144237
|
T | C | 9 | a0001c0002t0002g0031a0001c0002t0002g0150a0001c0002t0002g0151others(6): Show | 9 | HG02015.hp1 HG02132.hp2 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-9668T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111144237 | ||||||
| chr13:111144310
|
A | T | 2 | a0001c0001t0001g0144a0001c0001t0008g0017 | 2 | HG01109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.166-9595A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111144310 | ||||||
| chr13:111144339
|
G | A | 2 | a0001c0001t0001g0068a0001c0001t0004g0110 | 2 | HG02280.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.166-9566G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111144339 | ||||||
| chr13:111144436
|
T | C | 1 | a0001c0001t0006g0041 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.166-9469T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111144436 | ||||||
| chr13:111144626
|
G | A | 168 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(165): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.166-9279G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111144626 | ||||||
| chr13:111144648
|
G | A | 3 | a0001c0001t0016g0077a0001c0001t0034g0061a0001c0012t0030g0072 | 3 | HG01167.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.166-9257G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111144648 | ||||||
| chr13:111144899
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.166-9006G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111144899 | ||||||
| chr13:111145020
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.166-8885C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111145020 | ||||||
| chr13:111145033
|
C | CT | 163 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.166-8861dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111145033 | |||||
| chr13:111145044
|
T | TA | 3 | a0001c0001t0001g0049a0001c0001t0001g0172a0001c0001t0003g0179 | 3 | HG00639.hp1 HG01192.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.166-8856dupA | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111145044 | |||||
| chr13:111145084
|
C | T | 20 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(17): Show | 20 | HG01192.hp1 HG01257.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.166-8821C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111145084 | ||||||
| chr13:111145146
|
T | C | 1 | a0001c0001t0003g0088 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.166-8759T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111145146 | ||||||
| chr13:111145231
|
T | C | 42 | a0001c0001t0001g0016a0001c0001t0001g0066a0001c0001t0001g0074others(39): Show | 42 | HG00099.hp2 HG00642.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.166-8674T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111145231 | ||||||
| chr13:111145256
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.166-8649A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111145256 | ||||||
| chr13:111145412
|
C | T | 3 | a0001c0001t0007g0004a0001c0001t0007g0034a0001c0001t0007g0067 | 3 | HG01884.hp2 HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.166-8493C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111145412 | ||||||
| chr13:111145508
|
G | A | 1 | a0001c0001t0002g0251 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.166-8397G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111145508 | ||||||
| chr13:111145558
|
A | G | 2 | a0001c0001t0005g0102a0001c0001t0005g0103 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.166-8347A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111145558 | ||||||
| chr13:111145560
|
G | T | 17 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0052others(14): Show | 17 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.166-8345G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111145560 | ||||||
| chr13:111145573
|
G | A | 43 | a0001c0001t0001g0068a0001c0001t0001g0084a0001c0001t0002g0078others(40): Show | 43 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.166-8332G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111145573 | ||||||
| chr13:111145985
|
G | C | 1 | a0001c0001t0002g0029 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.166-7920G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111145985 | ||||||
| chr13:111146511
|
G | T | 3 | a0001c0001t0003g0107a0001c0001t0003g0136a0001c0001t0003g0215 | 3 | HG01891.hp2 HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.166-7394G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111146511 | ||||||
| chr13:111146516
|
A | G | 1 | a0001c0001t0017g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.166-7389A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111146516 | ||||||
| chr13:111146529
|
A | G | 1 | a0001c0004t0022g0209 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.166-7376A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111146529 | ||||||
| chr13:111146726
|
G | A | 1 | a0001c0001t0004g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.166-7179G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111146726 | ||||||
| chr13:111146882
|
C | T | 1 | a0001c0002t0002g0198 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.166-7023C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111146882 | ||||||
| chr13:111146920
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.166-6985A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111146920 | ||||||
| chr13:111147142
|
T | C | 21 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(18): Show | 21 | HG01081.hp1 HG01192.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-6763T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111147142 | ||||||
| chr13:111147152
|
T | C | 1 | a0001c0001t0002g0078 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.166-6753T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111147152 | ||||||
| chr13:111147295
|
C | T | 1 | a0001c0002t0002g0031 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.166-6610C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111147295 | ||||||
| chr13:111147385
|
T | G | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-6520T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111147385 | ||||||
| chr13:111147473
|
T | C | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.166-6432T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111147473 | ||||||
| chr13:111147570
|
C | A | 1 | a0001c0001t0017g0269 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.166-6335C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111147570 | ||||||
| chr13:111147598
|
C | T | 16 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0052others(13): Show | 16 | HG00099.hp1 HG00280.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.166-6307C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111147598 | ||||||
| chr13:111147599
|
G | A | 1 | a0001c0002t0002g0079 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.166-6306G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111147599 | ||||||
| chr13:111147610
|
G | C | 23 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(20): Show | 23 | HG01081.hp1 HG01192.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.166-6295G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111147610 | ||||||
| chr13:111147645
|
G | A | 1 | a0001c0004t0022g0208 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.166-6260G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111147645 | ||||||
| chr13:111147690
|
C | CT | 47 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(44): Show | 47 | HG00597.hp2 HG00639.hp1 HG01175.hp1 others(44): Show |
intron_variant | MODIFIER | c.166-6190dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111147690 | |||||
| chr13:111147690
|
C | CTT | 10 | a0001c0001t0001g0005a0001c0001t0001g0027a0001c0001t0001g0040others(7): Show | 10 | HG00741.hp2 HG01109.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.166-6191_166-6190d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111147690 | |||||
| chr13:111147690
|
C | CTTT | 11 | a0001c0001t0003g0107a0001c0001t0003g0136a0001c0001t0003g0215others(8): Show | 11 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.166-6192_166-6190d others(5): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111147690 | |||||
| chr13:111147690
|
CT | C | 65 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0039others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.166-6190delT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111147690 | |||||
| chr13:111147798
|
C | T | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-6107C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111147798 | ||||||
| chr13:111147846
|
C | T | 8 | a0001c0001t0003g0104a0001c0001t0003g0108a0001c0001t0003g0210others(5): Show | 8 | HG00099.hp2 HG01069.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-6059C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111147846 | ||||||
| chr13:111147859
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.166-6046G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111147859 | ||||||
| chr13:111147890
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(5): Show | 8 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-6015G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111147890 | ||||||
| chr13:111147919
|
G | C | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-5986G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111147919 | ||||||
| chr13:111147933
|
G | A | 83 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0106others(80): Show | 83 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.166-5972G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111147933 | ||||||
| chr13:111147988
|
T | C | 107 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0106others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.166-5917T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111147988 | ||||||
| chr13:111147993
|
A | G | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-5912A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111147993 | ||||||
| chr13:111148094
|
C | T | 98 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0106others(95): Show | 98 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.166-5811C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111148094 | ||||||
| chr13:111148168
|
A | T | 21 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(18): Show | 21 | HG01081.hp1 HG01192.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-5737A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111148168 | ||||||
| chr13:111148242
|
T | G | 21 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(18): Show | 21 | HG01081.hp1 HG01192.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-5663T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111148242 | ||||||
| chr13:111148277
|
A | G | 107 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0106others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.166-5628A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111148277 | ||||||
| chr13:111148436
|
G | A | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-5469G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111148436 | ||||||
| chr13:111148464
|
T | C | 2 | a0001c0001t0002g0011a0001c0001t0016g0012 | 2 | HG02895.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.166-5441T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111148464 | ||||||
| chr13:111149134
|
G | T | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-4771G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111149134 | ||||||
| chr13:111149179
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.166-4726G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111149179 | ||||||
| chr13:111149246
|
G | GA | 9 | a0001c0001t0001g0125a0001c0001t0009g0171a0001c0001t0009g0202others(6): Show | 9 | HG00741.hp2 NA18962.hp2 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-4648dupA | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111149246 | |||||
| chr13:111149313
|
A | G | 38 | a0001c0001t0001g0016a0001c0001t0001g0066a0001c0001t0001g0074others(35): Show | 38 | HG00099.hp2 HG00642.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.166-4592A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111149313 | ||||||
| chr13:111149361
|
T | C | 1 | a0001c0001t0003g0024 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.166-4544T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111149361 | ||||||
| chr13:111149562
|
C | T | 1 | a0001c0001t0006g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.166-4343C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111149562 | ||||||
| chr13:111149605
|
T | G | 1 | a0001c0015t0002g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.166-4300T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111149605 | ||||||
| chr13:111149716
|
G | A | 8 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(5): Show | 8 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-4189G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111149716 | ||||||
| chr13:111149804
|
A | G | 3 | a0001c0001t0001g0160a0001c0001t0006g0041a0001c0001t0006g0185 | 3 | NA18966.hp2 NA18999.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.166-4101A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111149804 | ||||||
| chr13:111149907
|
C | A | 3 | a0001c0016t0008g0227a0002c0009t0002g0069a0002c0009t0002g0112 | 3 | HG03486.hp1 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.166-3998C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111149907 | ||||||
| chr13:111150205
|
T | C | 3 | a0001c0001t0012g0001a0001c0007t0004g0059a0001c0007t0027g0054 | 3 | HG03139.hp1 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.166-3700T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111150205 | ||||||
| chr13:111150487
|
C | G | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-3418C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111150487 | ||||||
| chr13:111150652
|
C | T | 1 | a0001c0001t0003g0240 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.166-3253C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111150652 | ||||||
| chr13:111150740
|
T | A | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-3165T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111150740 | ||||||
| chr13:111150816
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.166-3089C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111150816 | ||||||
| chr13:111150827
|
G | C | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.166-3078G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111150827 | ||||||
| chr13:111151204
|
T | C | 28 | a0001c0001t0001g0040a0001c0001t0001g0047a0001c0001t0001g0048others(25): Show | 28 | HG00639.hp1 HG00741.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.166-2701T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111151204 | ||||||
| chr13:111151253
|
T | G | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-2652T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111151253 | ||||||
| chr13:111151457
|
A | G | 12 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(9): Show | 12 | HG01192.hp1 HG01243.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.166-2448A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111151457 | ||||||
| chr13:111151610
|
C | G | 7 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(4): Show | 7 | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-2295C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111151610 | ||||||
| chr13:111151617
|
G | A | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-2288G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111151617 | ||||||
| chr13:111151948
|
T | G | 1 | a0001c0002t0002g0189 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.166-1957T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111151948 | ||||||
| chr13:111152019
|
AT | A | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-1881delT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111152019 | |||||
| chr13:111152180
|
GAATT | G | 56 | a0001c0001t0001g0106a0001c0001t0001g0129a0001c0001t0001g0137others(53): Show | 56 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.166-1721_166-1718d others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | 111152180 | |||||
| chr13:111152214
|
A | T | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.166-1691A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111152214 | ||||||
| chr13:111152625
|
C | T | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.166-1280C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111152625 | ||||||
| chr13:111152638
|
C | T | 2 | a0001c0002t0002g0199a0001c0002t0002g0204 | 2 | NA18971.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.166-1267C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111152638 | ||||||
| chr13:111152760
|
T | G | 97 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0106others(94): Show | 97 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.166-1145T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111152760 | ||||||
| chr13:111152763
|
G | A | 4 | a0001c0001t0002g0091a0001c0001t0002g0099a0001c0001t0015g0271others(1): Show | 4 | HG03453.hp2 HG03516.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.166-1142G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111152763 | ||||||
| chr13:111152943
|
C | T | 1 | a0001c0001t0013g0154 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.166-962C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111152943 | ||||||
| chr13:111152954
|
G | C | 2 | a0001c0001t0001g0049a0001c0001t0001g0172 | 2 | HG00639.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.166-951G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111152954 | ||||||
| chr13:111153065
|
G | A | 233 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.166-840G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111153065 | ||||||
| chr13:111153066
|
C | T | 3 | a0001c0001t0016g0077a0001c0001t0034g0061a0001c0012t0030g0072 | 3 | HG01167.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.166-839C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111153066 | ||||||
| chr13:111153178
|
A | T | 186 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0039others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.166-727A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111153178 | ||||||
| chr13:111153234
|
A | T | 5 | a0001c0001t0001g0005a0001c0001t0003g0107a0001c0001t0003g0136others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-671A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111153234 | ||||||
| chr13:111153327
|
C | T | 1 | a0001c0001t0001g0018 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.166-578C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111153327 | ||||||
| chr13:111153393
|
G | A | 3 | a0001c0001t0001g0084a0001c0001t0016g0077a0001c0001t0034g0061 | 3 | HG01167.hp2 HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.166-512G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111153393 | ||||||
| chr13:111153411
|
T | A | 95 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0106others(92): Show | 95 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.166-494T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111153411 | ||||||
| chr13:111153430
|
G | A | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.166-475G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111153430 | ||||||
| chr13:111153472
|
G | A | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-433G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111153472 | ||||||
| chr13:111153475
|
C | T | 1 | a0001c0001t0003g0262 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.166-430C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111153475 | ||||||
| chr13:111153611
|
C | A | 1 | a0001c0002t0031g0130 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.166-294C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111153611 | ||||||
| chr13:111153615
|
G | T | 1 | a0001c0001t0007g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.166-290G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111153615 | ||||||
| chr13:111153658
|
C | T | 17 | a0001c0001t0001g0160a0001c0001t0003g0128a0001c0001t0003g0267others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.166-247C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111153658 | ||||||
| chr13:111153693
|
T | G | 17 | a0001c0001t0001g0160a0001c0001t0003g0128a0001c0001t0003g0267others(14): Show | 17 | HG00642.hp1 HG01081.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.166-212T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111153693 | ||||||
| chr13:111153720
|
G | A | 1 | a0001c0001t0008g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.166-185G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111153720 | ||||||
| chr13:111153870
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.166-35G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111153870 | ||||||
| chr13:111153898
|
A | G | 104 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0129others(101): Show | 104 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(101): Show |
splice_region_variant&intron_variant | LOW | c.166-7A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | chr13 | 111153898 | ||||||
| chr13:111154384
|
A | G | 13 | a0001c0001t0003g0024a0001c0001t0003g0119a0001c0001t0006g0083others(10): Show | 13 | HG00738.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.252+393A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111154384 | ||||||
| chr13:111154460
|
C | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(36): Show | 39 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.252+469C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111154460 | ||||||
| chr13:111154765
|
A | G | 1 | a0001c0002t0002g0082 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.252+774A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111154765 | ||||||
| chr13:111154955
|
C | G | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252+964C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111154955 | ||||||
| chr13:111154957
|
T | C | 92 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0097others(89): Show | 92 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.252+966T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111154957 | ||||||
| chr13:111155028
|
A | C | 3 | a0001c0001t0006g0032a0001c0002t0001g0182a0001c0002t0002g0174 | 3 | HG00558.hp2 NA18964.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.252+1037A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111155028 | ||||||
| chr13:111155071
|
G | A | 9 | a0001c0002t0002g0031a0001c0002t0002g0150a0001c0002t0002g0151others(6): Show | 9 | HG02015.hp1 HG02132.hp2 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.252+1080G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111155071 | ||||||
| chr13:111155201
|
C | T | 19 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(16): Show | 19 | HG00140.hp1 HG01099.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.252+1210C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111155201 | ||||||
| chr13:111155237
|
T | C | 1 | a0001c0001t0004g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.252+1246T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111155237 | ||||||
| chr13:111155285
|
T | C | 3 | a0001c0001t0005g0212a0001c0006t0012g0121a0001c0006t0012g0124 | 3 | HG00741.hp1 HG01081.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.252+1294T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111155285 | ||||||
| chr13:111155301
|
C | T | 201 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.252+1310C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111155301 | ||||||
| chr13:111155325
|
C | G | 3 | a0001c0002t0021g0255a0001c0002t0021g0256a0001c0002t0031g0130 | 3 | NA18957.hp1 NA18979.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.252+1334C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111155325 | ||||||
| chr13:111155512
|
C | T | 5 | a0001c0001t0001g0106a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG00639.hp2 HG01243.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+1521C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111155512 | ||||||
| chr13:111155537
|
G | A | 1 | a0001c0002t0006g0236 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.252+1546G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111155537 | ||||||
| chr13:111155640
|
T | C | 1 | a0001c0005t0020g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.252+1649T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111155640 | ||||||
| chr13:111155766
|
A | T | 1 | a0001c0001t0006g0083 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.252+1775A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111155766 | ||||||
| chr13:111155841
|
C | G | 1 | a0001c0002t0002g0194 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.252+1850C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111155841 | ||||||
| chr13:111155841
|
C | T | 1 | a0001c0001t0004g0254 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.252+1850C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111155841 | ||||||
| chr13:111155914
|
TAAAC | T | 7 | a0001c0001t0003g0107a0001c0001t0003g0136a0001c0001t0003g0178others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+1928_252+1931d others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111155914 | |||||
| chr13:111155915
|
A | G | 201 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.252+1924A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111155915 | ||||||
| chr13:111155942
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0229 | 2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.252+1951C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111155942 | ||||||
| chr13:111155954
|
G | A | 1 | a0001c0001t0005g0212 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.252+1963G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111155954 | ||||||
| chr13:111155954
|
G | C | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252+1963G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111155954 | ||||||
| chr13:111156080
|
CAAA | C | 8 | a0001c0001t0003g0089a0001c0001t0003g0184a0001c0001t0005g0062others(5): Show | 8 | HG01109.hp1 HG02257.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.252+2109_252+2111d others(5): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111156080 | |||||
| chr13:111156080
|
CAAAA | C | 150 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0048others(147): Show | 150 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.252+2108_252+2111d others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111156080 | |||||
| chr13:111156080
|
CAAAAA | C | 62 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(59): Show | 62 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.252+2107_252+2111d others(7): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111156080 | |||||
| chr13:111156080
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0018g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.252+2101_252+2111d others(13): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111156080 | |||||
| chr13:111156141
|
C | G | 1 | a0001c0002t0002g0190 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.252+2150C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111156141 | ||||||
| chr13:111156211
|
AAG | A | 201 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.252+2225_252+2226d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111156211 | |||||
| chr13:111156285
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.252+2294G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111156285 | ||||||
| chr13:111156348
|
A | T | 6 | a0001c0001t0003g0119a0001c0001t0006g0083a0001c0001t0006g0234others(3): Show | 6 | HG00738.hp1 HG03195.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.252+2357A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111156348 | ||||||
| chr13:111156401
|
T | C | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.252+2410T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111156401 | ||||||
| chr13:111156566
|
T | G | 42 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.252+2575T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111156566 | ||||||
| chr13:111156575
|
A | G | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.252+2584A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111156575 | ||||||
| chr13:111156578
|
C | T | 41 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(38): Show | 41 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.252+2587C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111156578 | ||||||
| chr13:111156602
|
G | A | 1 | a0001c0002t0002g0033 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.252+2611G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111156602 | ||||||
| chr13:111156622
|
A | G | 5 | a0001c0001t0001g0106a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG00639.hp2 HG01243.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+2631A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111156622 | ||||||
| chr13:111156745
|
G | A | 5 | a0001c0001t0001g0106a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG00639.hp2 HG01243.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+2754G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111156745 | ||||||
| chr13:111156961
|
T | A | 2 | a0001c0001t0001g0051a0001c0001t0005g0230 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.252+2970T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111156961 | ||||||
| chr13:111157037
|
G | A | 4 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017others(1): Show | 4 | HG01109.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+3046G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111157037 | ||||||
| chr13:111157116
|
G | T | 201 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.252+3125G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111157116 | ||||||
| chr13:111157181
|
C | T | 221 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.252+3190C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111157181 | ||||||
| chr13:111157189
|
C | T | 41 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(38): Show | 41 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.252+3198C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111157189 | ||||||
| chr13:111157289
|
AT | A | 219 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(216): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.252+3312delT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111157289 | |||||
| chr13:111157561
|
C | T | 201 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(198): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.252+3570C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111157561 | ||||||
| chr13:111157660
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.252+3669G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111157660 | ||||||
| chr13:111157894
|
C | T | 8 | a0001c0001t0003g0119a0001c0001t0006g0083a0001c0001t0006g0234others(5): Show | 8 | HG00738.hp1 HG03195.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.252+3903C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111157894 | ||||||
| chr13:111158071
|
G | C | 1 | a0001c0001t0002g0251 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.252+4080G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111158071 | ||||||
| chr13:111158418
|
T | C | 1 | a0001c0001t0011g0055 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.252+4427T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111158418 | ||||||
| chr13:111158427
|
T | C | 13 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0052others(10): Show | 13 | HG00099.hp1 HG00280.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.252+4436T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111158427 | ||||||
| chr13:111158479
|
G | A | 2 | a0001c0001t0004g0133a0001c0001t0004g0134 | 2 | NA19066.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.252+4488G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111158479 | ||||||
| chr13:111158480
|
C | A | 42 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0066others(39): Show | 42 | HG00099.hp2 HG00642.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.252+4489C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111158480 | ||||||
| chr13:111158820
|
C | T | 7 | a0001c0001t0003g0107a0001c0001t0003g0136a0001c0001t0003g0178others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+4829C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111158820 | ||||||
| chr13:111159081
|
T | C | 2 | a0001c0002t0021g0255a0001c0002t0021g0256 | 2 | NA18957.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.252+5090T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111159081 | ||||||
| chr13:111159083
|
T | G | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252+5092T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111159083 | ||||||
| chr13:111159224
|
T | A | 1 | a0001c0001t0004g0241 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.252+5233T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111159224 | ||||||
| chr13:111159504
|
A | G | 1 | a0001c0015t0002g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.252+5513A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111159504 | ||||||
| chr13:111159626
|
A | G | 14 | a0001c0001t0001g0113a0001c0001t0001g0253a0001c0001t0003g0128others(11): Show | 14 | HG01081.hp1 HG01257.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.252+5635A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111159626 | ||||||
| chr13:111159675
|
G | T | 19 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(16): Show | 19 | HG00140.hp1 HG01099.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.252+5684G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111159675 | ||||||
| chr13:111159883
|
CCT | C | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+5895_252+5896d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111159883 | |||||
| chr13:111160334
|
G | GT | 22 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(19): Show | 22 | HG00639.hp2 HG01243.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.252+6355dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111160334 | |||||
| chr13:111160482
|
G | A | 12 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.252+6491G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111160482 | ||||||
| chr13:111160615
|
T | G | 5 | a0001c0001t0002g0091a0001c0001t0002g0099a0001c0001t0003g0025others(2): Show | 5 | HG02976.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+6624T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111160615 | ||||||
| chr13:111161108
|
AT | A | 40 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.252+7118delT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111161108 | ||||||
| chr13:111161115
|
T | C | 20 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(17): Show | 20 | HG00140.hp1 HG01099.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.252+7124T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111161115 | ||||||
| chr13:111161277
|
C | T | 3 | a0001c0001t0008g0035a0001c0016t0008g0227a0007c0010t0001g0095 | 3 | HG03486.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.252+7286C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111161277 | ||||||
| chr13:111161343
|
C | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0066others(55): Show | 58 | HG00099.hp2 HG00642.hp1 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.252+7352C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111161343 | ||||||
| chr13:111161344
|
G | A | 3 | a0001c0001t0012g0001a0001c0007t0004g0059a0001c0007t0027g0054 | 3 | HG03139.hp1 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.252+7353G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111161344 | ||||||
| chr13:111161477
|
G | A | 5 | a0001c0001t0001g0106a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG00639.hp2 HG01243.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+7486G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111161477 | ||||||
| chr13:111161699
|
G | A | 1 | a0001c0001t0005g0116 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.252+7708G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111161699 | ||||||
| chr13:111161742
|
A | AT | 42 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.252+7761dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111161742 | |||||
| chr13:111161757
|
A | G | 1 | a0001c0015t0002g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.252+7766A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111161757 | ||||||
| chr13:111161858
|
A | G | 224 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.252+7867A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111161858 | ||||||
| chr13:111161872
|
T | C | 1 | a0001c0001t0006g0234 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.252+7881T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111161872 | ||||||
| chr13:111161973
|
C | G | 4 | a0001c0001t0003g0107a0001c0001t0003g0136a0001c0001t0003g0215others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+7982C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111161973 | ||||||
| chr13:111162037
|
T | C | 1 | a0001c0004t0022g0208 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.252+8046T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111162037 | ||||||
| chr13:111162086
|
A | T | 1 | a0001c0001t0001g0144 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.252+8095A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111162086 | ||||||
| chr13:111162087
|
C | G | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+8096C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111162087 | ||||||
| chr13:111162192
|
A | T | 1 | a0001c0001t0001g0092 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.252+8201A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111162192 | ||||||
| chr13:111162261
|
C | T | 19 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(16): Show | 19 | HG00140.hp1 HG01099.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.252+8270C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111162261 | ||||||
| chr13:111162287
|
G | A | 1 | a0001c0001t0005g0116 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.252+8296G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111162287 | ||||||
| chr13:111162309
|
G | A | 5 | a0001c0001t0001g0106a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG00639.hp2 HG01243.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+8318G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111162309 | ||||||
| chr13:111162331
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.252+8340C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111162331 | ||||||
| chr13:111162412
|
T | G | 2 | a0001c0001t0004g0122a0001c0001t0011g0055 | 2 | HG02055.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.252+8421T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111162412 | ||||||
| chr13:111162664
|
G | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.252+8673G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111162664 | ||||||
| chr13:111162710
|
T | G | 1 | a0001c0001t0003g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.252+8719T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111162710 | ||||||
| chr13:111162794
|
T | G | 1 | a0001c0001t0001g0047 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.252+8803T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111162794 | ||||||
| chr13:111162931
|
A | G | 2 | a0001c0001t0001g0138a0001c0001t0006g0090 | 2 | HG02622.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.252+8940A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111162931 | ||||||
| chr13:111163053
|
T | C | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252+9062T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111163053 | ||||||
| chr13:111163313
|
T | C | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.252+9322T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111163313 | ||||||
| chr13:111163721
|
G | A | 6 | a0001c0001t0007g0004a0001c0001t0007g0009a0001c0001t0007g0028others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.252+9730G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111163721 | ||||||
| chr13:111163774
|
G | T | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252+9783G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111163774 | ||||||
| chr13:111163788
|
G | A | 5 | a0001c0001t0001g0106a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG00639.hp2 HG01243.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+9797G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111163788 | ||||||
| chr13:111163821
|
C | T | 8 | a0001c0001t0003g0119a0001c0001t0006g0083a0001c0001t0006g0234others(5): Show | 8 | HG00738.hp1 HG03195.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.252+9830C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111163821 | ||||||
| chr13:111163897
|
G | T | 6 | a0001c0002t0002g0031a0001c0002t0002g0151a0001c0002t0002g0152others(3): Show | 6 | NA18941.hp1 NA18955.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.252+9906G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111163897 | ||||||
| chr13:111163954
|
G | A | 1 | a0001c0001t0002g0078 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.252+9963G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111163954 | ||||||
| chr13:111163983
|
T | C | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+9992T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111163983 | ||||||
| chr13:111163987
|
G | A | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252+9996G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111163987 | ||||||
| chr13:111164061
|
ATTAT | A | 46 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0066others(43): Show | 46 | HG00642.hp1 HG00741.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.252+10074_252+1007 others(8): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111164061 | |||||
| chr13:111164225
|
C | T | 1 | a0004c0017t0003g0120 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.252+10234C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111164225 | ||||||
| chr13:111164349
|
G | A | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252+10358G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111164349 | ||||||
| chr13:111164508
|
A | G | 1 | a0001c0001t0016g0077 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.252+10517A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111164508 | ||||||
| chr13:111164658
|
A | G | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252+10667A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111164658 | ||||||
| chr13:111164673
|
A | G | 1 | a0001c0002t0002g0033 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.252+10682A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111164673 | ||||||
| chr13:111165200
|
A | G | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252+11209A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111165200 | ||||||
| chr13:111165318
|
A | G | 221 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(218): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.252+11327A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111165318 | ||||||
| chr13:111165370
|
G | A | 1 | a0001c0001t0005g0116 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.252+11379G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111165370 | ||||||
| chr13:111165428
|
G | A | 2 | a0001c0002t0002g0147a0001c0002t0002g0148 | 2 | HG01175.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.252+11437G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111165428 | ||||||
| chr13:111165457
|
A | G | 2 | a0001c0002t0002g0147a0001c0002t0002g0148 | 2 | HG01175.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.252+11466A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111165457 | ||||||
| chr13:111165511
|
A | G | 1 | a0001c0001t0017g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.252+11520A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111165511 | ||||||
| chr13:111165595
|
C | T | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.252+11604C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111165595 | ||||||
| chr13:111165889
|
A | G | 3 | a0001c0001t0012g0001a0001c0007t0004g0059a0001c0007t0027g0054 | 3 | HG03139.hp1 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.252+11898A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111165889 | ||||||
| chr13:111166048
|
T | A | 1 | a0001c0001t0007g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.252+12057T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111166048 | ||||||
| chr13:111166050
|
C | G | 3 | a0001c0001t0016g0077a0001c0001t0034g0061a0001c0012t0030g0072 | 3 | HG01167.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.252+12059C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111166050 | ||||||
| chr13:111166133
|
G | A | 19 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(16): Show | 19 | HG00140.hp1 HG01099.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.252+12142G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111166133 | ||||||
| chr13:111166164
|
T | G | 2 | a0001c0002t0002g0151a0001c0002t0002g0152 | 2 | NA18941.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.252+12173T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111166164 | ||||||
| chr13:111166189
|
C | T | 9 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(6): Show | 9 | HG02055.hp1 NA18962.hp2 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.252+12198C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111166189 | ||||||
| chr13:111166252
|
C | T | 19 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(16): Show | 19 | HG00140.hp1 HG01099.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.252+12261C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111166252 | ||||||
| chr13:111166388
|
G | C | 1 | a0007c0010t0001g0095 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.252+12397G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111166388 | ||||||
| chr13:111166395
|
G | C | 7 | a0001c0001t0003g0107a0001c0001t0003g0136a0001c0001t0003g0178others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+12404G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111166395 | ||||||
| chr13:111166415
|
A | G | 1 | a0001c0001t0003g0267 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.252+12424A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111166415 | ||||||
| chr13:111166485
|
A | G | 226 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.252+12494A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111166485 | ||||||
| chr13:111166557
|
C | G | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252+12566C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111166557 | ||||||
| chr13:111166566
|
C | A | 10 | a0001c0001t0003g0240a0001c0001t0003g0245a0001c0001t0003g0249others(7): Show | 10 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(7): Show |
intron_variant | MODIFIER | c.252+12575C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111166566 | ||||||
| chr13:111166631
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.252+12640G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111166631 | ||||||
| chr13:111166681
|
A | T | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252+12690A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111166681 | ||||||
| chr13:111166682
|
A | T | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252+12691A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111166682 | ||||||
| chr13:111166685
|
T | C | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252+12694T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111166685 | ||||||
| chr13:111166720
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.252+12729G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111166720 | ||||||
| chr13:111166996
|
G | A | 40 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.252+13005G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111166996 | ||||||
| chr13:111167034
|
G | A | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.252+13043G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111167034 | ||||||
| chr13:111167320
|
T | A | 1 | a0001c0005t0020g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.252+13329T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111167320 | ||||||
| chr13:111167445
|
C | A | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+13454C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111167445 | ||||||
| chr13:111167588
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.252+13597G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111167588 | ||||||
| chr13:111167612
|
A | G | 3 | a0001c0001t0012g0001a0001c0007t0004g0059a0001c0007t0027g0054 | 3 | HG03139.hp1 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.252+13621A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111167612 | ||||||
| chr13:111168025
|
C | T | 2 | a0001c0001t0017g0270a0001c0014t0001g0058 | 2 | HG01192.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.252+14034C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111168025 | ||||||
| chr13:111168026
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.252+14035G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111168026 | ||||||
| chr13:111168042
|
T | TG | 5 | a0001c0001t0001g0106a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG00639.hp2 HG01243.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+14053dupG | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111168042 | |||||
| chr13:111168139
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.252+14148C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111168139 | ||||||
| chr13:111168187
|
G | T | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18962.hp2 NA18982.hp1 NA19000.hp1 others(5): Show |
intron_variant | MODIFIER | c.252+14196G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111168187 | ||||||
| chr13:111168224
|
T | C | 3 | a0001c0002t0021g0255a0001c0002t0021g0256a0001c0002t0031g0130 | 3 | NA18957.hp1 NA18979.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.252+14233T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111168224 | ||||||
| chr13:111168266
|
T | TGCGGTGT others(19): Show |
7 | a0001c0001t0003g0107a0001c0001t0003g0136a0001c0001t0003g0178others(4): Show | 7 | HG00140.hp1 HG01099.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.252+14276_252+1430 others(30): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111168266 | |||||
| chr13:111168553
|
G | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(39): Show | 42 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.252+14562G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111168553 | ||||||
| chr13:111168847
|
A | G | 1 | a0001c0001t0003g0179 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.252+14856A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111168847 | ||||||
| chr13:111168874
|
G | A | 8 | a0001c0001t0003g0119a0001c0001t0006g0083a0001c0001t0006g0234others(5): Show | 8 | HG00738.hp1 HG03195.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.252+14883G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111168874 | ||||||
| chr13:111168900
|
A | C | 12 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.252+14909A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111168900 | ||||||
| chr13:111168942
|
G | C | 222 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.252+14951G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111168942 | ||||||
| chr13:111169409
|
A | G | 39 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(36): Show | 39 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.252+15418A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111169409 | ||||||
| chr13:111169411
|
C | G | 1 | a0001c0001t0004g0254 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.252+15420C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111169411 | ||||||
| chr13:111169420
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.252+15429C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111169420 | ||||||
| chr13:111169430
|
C | T | 2 | a0001c0001t0002g0029a0001c0001t0002g0156 | 2 | NA19009.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.252+15439C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111169430 | ||||||
| chr13:111169478
|
C | T | 39 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(36): Show | 39 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.252+15487C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111169478 | ||||||
| chr13:111169539
|
A | G | 1 | a0001c0001t0006g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.252+15548A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111169539 | ||||||
| chr13:111169592
|
C | T | 2 | a0001c0001t0004g0247a0001c0001t0004g0248 | 2 | HG00280.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.252+15601C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111169592 | ||||||
| chr13:111169794
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.252+15803C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111169794 | ||||||
| chr13:111169813
|
T | C | 20 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(17): Show | 20 | HG00140.hp1 HG01099.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.252+15822T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111169813 | ||||||
| chr13:111169988
|
CAGGCCCC others(40): Show |
C | 4 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017others(1): Show | 4 | HG01109.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+16027_252+1607 others(51): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111169988 | |||||
| chr13:111170010
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.252+16019G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111170010 | ||||||
| chr13:111170224
|
A | AGTAGCTG others(5): Show |
61 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0066others(58): Show | 61 | HG00099.hp2 HG00642.hp1 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.252+16243_252+1624 others(16): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111170224 | |||||
| chr13:111170286
|
C | T | 5 | a0001c0001t0002g0091a0001c0001t0002g0099a0001c0001t0003g0025others(2): Show | 5 | HG02976.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+16295C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111170286 | ||||||
| chr13:111170350
|
G | A | 1 | a0001c0002t0002g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.252+16359G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111170350 | ||||||
| chr13:111170544
|
A | G | 1 | a0001c0001t0005g0115 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.252+16553A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111170544 | ||||||
| chr13:111170715
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0028g0127 | 2 | HG01496.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.252+16724C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111170715 | ||||||
| chr13:111170772
|
G | A | 1 | a0001c0001t0005g0212 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.252+16781G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111170772 | ||||||
| chr13:111170945
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.252+16954A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111170945 | ||||||
| chr13:111170957
|
T | C | 20 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(17): Show | 20 | HG00140.hp1 HG01099.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.252+16966T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111170957 | ||||||
| chr13:111170967
|
T | C | 3 | a0001c0001t0012g0001a0001c0007t0004g0059a0001c0007t0027g0054 | 3 | HG03139.hp1 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.252+16976T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111170967 | ||||||
| chr13:111171338
|
G | A | 1 | a0001c0001t0004g0254 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.252+17347G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111171338 | ||||||
| chr13:111171640
|
G | C | 5 | a0001c0001t0002g0091a0001c0001t0002g0099a0001c0001t0003g0025others(2): Show | 5 | HG02976.hp1 HG03453.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+17649G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111171640 | ||||||
| chr13:111171736
|
G | C | 1 | a0001c0001t0001g0137 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.252+17745G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111171736 | ||||||
| chr13:111171841
|
TG | T | 3 | a0001c0001t0016g0077a0001c0001t0034g0061a0001c0012t0030g0072 | 3 | HG01167.hp2 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.252+17854delG | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111171841 | |||||
| chr13:111171852
|
C | T | 1 | a0001c0001t0005g0230 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.252+17861C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111171852 | ||||||
| chr13:111171872
|
G | C | 2 | a0001c0001t0003g0104a0001c0001t0003g0108 | 2 | HG00099.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.252+17881G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111171872 | ||||||
| chr13:111171917
|
A | C | 19 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(16): Show | 19 | HG00140.hp1 HG01099.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.252+17926A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111171917 | ||||||
| chr13:111172035
|
G | A | 5 | a0001c0001t0001g0106a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG00639.hp2 HG01243.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+18044G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172035 | ||||||
| chr13:111172109
|
C | T | 1 | a0001c0002t0002g0169 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.252+18118C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172109 | ||||||
| chr13:111172146
|
C | T | 1 | a0001c0002t0002g0149 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.252+18155C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172146 | ||||||
| chr13:111172203
|
T | C | 5 | a0001c0001t0001g0106a0001c0001t0001g0167a0001c0001t0001g0168others(2): Show | 5 | HG00639.hp2 HG01243.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+18212T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172203 | ||||||
| chr13:111172307
|
A | G | 3 | a0001c0001t0003g0107a0001c0001t0003g0136a0001c0001t0003g0215 | 3 | HG01891.hp2 HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.252+18316A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172307 | ||||||
| chr13:111172336
|
C | T | 2 | a0001c0002t0001g0170a0001c0002t0024g0183 | 2 | HG01257.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.252+18345C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172336 | ||||||
| chr13:111172397
|
G | C | 2 | a0001c0006t0012g0121a0001c0006t0012g0124 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.252+18406G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172397 | ||||||
| chr13:111172442
|
C | G | 5 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0011g0070others(2): Show | 5 | HG01891.hp1 HG03041.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+18451C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172442 | ||||||
| chr13:111172519
|
C | T | 1 | a0001c0001t0023g0037 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.252+18528C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172519 | ||||||
| chr13:111172605
|
C | G | 12 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.252+18614C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172605 | ||||||
| chr13:111172710
|
C | G | 1 | a0001c0001t0017g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.252+18719C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172710 | ||||||
| chr13:111172739
|
A | G | 43 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(40): Show | 43 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.252+18748A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172739 | ||||||
| chr13:111172740
|
G | T | 2 | a0001c0001t0011g0076a0001c0001t0026g0053 | 2 | NA19240.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.252+18749G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172740 | ||||||
| chr13:111172792
|
T | C | 1 | a0001c0001t0003g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.252+18801T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172792 | ||||||
| chr13:111172799
|
G | A | 1 | a0001c0002t0010g0197 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.252+18808G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172799 | ||||||
| chr13:111172823
|
T | TCGCACAA others(3): Show |
1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18832_252+1883 others(14): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172823 | ||||||
| chr13:111172824
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18833T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172824 | ||||||
| chr13:111172831
|
T | A | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18840T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172831 | ||||||
| chr13:111172833
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18842C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172833 | ||||||
| chr13:111172836
|
A | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18845A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172836 | ||||||
| chr13:111172837
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18846C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172837 | ||||||
| chr13:111172838
|
T | G | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18847T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172838 | ||||||
| chr13:111172839
|
A | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18848A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172839 | ||||||
| chr13:111172841
|
G | A | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18850G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172841 | ||||||
| chr13:111172844
|
T | G | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18853T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172844 | ||||||
| chr13:111172845
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.252+18854A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172845 | ||||||
| chr13:111172847
|
C | G | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18856C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172847 | ||||||
| chr13:111172849
|
G | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18858G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172849 | ||||||
| chr13:111172851
|
T | G | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18860T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172851 | ||||||
| chr13:111172852
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18861T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172852 | ||||||
| chr13:111172853
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18862T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172853 | ||||||
| chr13:111172855
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18864T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172855 | ||||||
| chr13:111172857
|
G | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18866G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172857 | ||||||
| chr13:111172858
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18867T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172858 | ||||||
| chr13:111172865
|
T | A | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18874T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172865 | ||||||
| chr13:111172866
|
T | G | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18875T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172866 | ||||||
| chr13:111172868
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18877C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172868 | ||||||
| chr13:111172869
|
T | A | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18878T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172869 | ||||||
| chr13:111172871
|
A | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18880A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172871 | ||||||
| chr13:111172873
|
G | A | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18882G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172873 | ||||||
| chr13:111172877
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18886C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172877 | ||||||
| chr13:111172880
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18889T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172880 | ||||||
| chr13:111172884
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18893C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172884 | ||||||
| chr13:111172886
|
C | A | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18895C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172886 | ||||||
| chr13:111172888
|
C | A | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18897C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172888 | ||||||
| chr13:111172891
|
T | A | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18900T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172891 | ||||||
| chr13:111172892
|
T | A | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18901T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172892 | ||||||
| chr13:111172894
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18903T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172894 | ||||||
| chr13:111172895
|
A | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18904A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172895 | ||||||
| chr13:111172897
|
T | A | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18906T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172897 | ||||||
| chr13:111172902
|
A | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18911A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172902 | ||||||
| chr13:111172903
|
T | G | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18912T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172903 | ||||||
| chr13:111172906
|
G | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18915G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172906 | ||||||
| chr13:111172908
|
G | A | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18917G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172908 | ||||||
| chr13:111172909
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18918T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172909 | ||||||
| chr13:111172917
|
T | A | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18926T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172917 | ||||||
| chr13:111172918
|
T | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18927T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172918 | ||||||
| chr13:111172919
|
G | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18928G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172919 | ||||||
| chr13:111172920
|
A | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18929A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172920 | ||||||
| chr13:111172921
|
G | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18930G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172921 | ||||||
| chr13:111172922
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18931C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172922 | ||||||
| chr13:111172923
|
A | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18932A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172923 | ||||||
| chr13:111172928
|
A | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18937A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172928 | ||||||
| chr13:111172929
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18938A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172929 | ||||||
| chr13:111172930
|
A | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18939A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172930 | ||||||
| chr13:111172934
|
G | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18943G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172934 | ||||||
| chr13:111172942
|
A | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18951A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172942 | ||||||
| chr13:111172943
|
A | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18952A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172943 | ||||||
| chr13:111172945
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18954A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172945 | ||||||
| chr13:111172950
|
A | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18959A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172950 | ||||||
| chr13:111172952
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18961A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172952 | ||||||
| chr13:111172953
|
C | G | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18962C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172953 | ||||||
| chr13:111172957
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18966C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172957 | ||||||
| chr13:111172960
|
G | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18969G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172960 | ||||||
| chr13:111172961
|
G | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18970G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172961 | ||||||
| chr13:111172963
|
C | A | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18972C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172963 | ||||||
| chr13:111172965
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18974C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172965 | ||||||
| chr13:111172970
|
A | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18979A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172970 | ||||||
| chr13:111172971
|
T | G | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18980T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172971 | ||||||
| chr13:111172973
|
T | G | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18982T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172973 | ||||||
| chr13:111172976
|
G | A | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18985G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172976 | ||||||
| chr13:111172979
|
GAGGGATG others(4): Show |
G | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+18990_252+1900 others(15): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111172979 | |||||
| chr13:111172994
|
T | A | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+19003T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111172994 | ||||||
| chr13:111173001
|
A | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+19010A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111173001 | ||||||
| chr13:111173002
|
G | C | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+19011G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111173002 | ||||||
| chr13:111173009
|
A | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+19018A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111173009 | ||||||
| chr13:111173010
|
A | T | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.252+19019A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111173010 | ||||||
| chr13:111173074
|
G | A | 1 | a0001c0001t0003g0274 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.252+19083G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111173074 | ||||||
| chr13:111173123
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.252+19132C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111173123 | ||||||
| chr13:111173124
|
A | C | 1 | a0001c0002t0002g0157 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.252+19133A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111173124 | ||||||
| chr13:111173437
|
T | A | 1 | a0001c0001t0003g0145 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.252+19446T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111173437 | ||||||
| chr13:111173777
|
A | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(35): Show | 38 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.252+19786A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111173777 | ||||||
| chr13:111173825
|
G | T | 40 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(37): Show | 40 | HG00099.hp1 HG00280.hp1 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.252+19834G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111173825 | ||||||
| chr13:111173945
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.252+19954A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111173945 | ||||||
| chr13:111174053
|
G | C | 2 | a0001c0001t0001g0051a0001c0001t0005g0230 | 2 | HG01071.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.252+20062G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111174053 | ||||||
| chr13:111174104
|
C | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.252+20113C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111174104 | ||||||
| chr13:111174307
|
C | T | 5 | a0001c0001t0003g0178a0001c0001t0003g0216a0001c0001t0003g0262others(2): Show | 5 | HG00140.hp1 HG01099.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.252+20316C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111174307 | ||||||
| chr13:111174399
|
C | G | 10 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(7): Show | 10 | NA18962.hp1 NA18962.hp2 NA18982.hp1 others(7): Show |
intron_variant | MODIFIER | c.252+20408C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111174399 | ||||||
| chr13:111174420
|
C | T | 1 | a0001c0001t0003g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.252+20429C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111174420 | ||||||
| chr13:111174523
|
C | T | 1 | a0001c0001t0032g0030 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.252+20532C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111174523 | ||||||
| chr13:111174569
|
C | T | 1 | a0001c0002t0002g0157 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.252+20578C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111174569 | ||||||
| chr13:111174584
|
C | T | 8 | a0001c0001t0001g0068a0001c0001t0004g0110a0001c0001t0007g0004others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.252+20593C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111174584 | ||||||
| chr13:111174820
|
T | C | 53 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0049others(50): Show | 53 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.252+20829T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111174820 | ||||||
| chr13:111174840
|
ACT | A | 15 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0068others(12): Show | 15 | HG01192.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.252+20851_252+2085 others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111174840 | |||||
| chr13:111174863
|
A | G | 3 | a0001c0001t0003g0252a0001c0001t0008g0035a0001c0001t0008g0111 | 3 | HG02809.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.252+20872A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111174863 | ||||||
| chr13:111174882
|
C | T | 11 | a0001c0001t0001g0039a0001c0001t0001g0049a0001c0001t0001g0068others(8): Show | 11 | HG00558.hp1 HG00639.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.252+20891C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111174882 | ||||||
| chr13:111174920
|
G | C | 2 | a0001c0001t0001g0084a0001c0001t0003g0025 | 2 | HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.252+20929G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111174920 | ||||||
| chr13:111174931
|
A | G | 1 | a0001c0002t0002g0033 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.252+20940A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111174931 | ||||||
| chr13:111175116
|
A | G | 2 | a0002c0009t0002g0069a0002c0009t0002g0112 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.252+21125A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111175116 | ||||||
| chr13:111175123
|
T | C | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+21132T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111175123 | ||||||
| chr13:111175249
|
G | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0074a0001c0001t0011g0070 | 3 | HG02647.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.252+21258G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111175249 | ||||||
| chr13:111175454
|
T | C | 5 | a0001c0001t0001g0005a0001c0001t0003g0119a0001c0001t0018g0020others(2): Show | 5 | HG00738.hp1 HG03195.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.252+21463T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111175454 | ||||||
| chr13:111175475
|
C | T | 5 | a0001c0001t0009g0202a0001c0001t0009g0258a0001c0001t0009g0259others(2): Show | 5 | NA18941.hp2 NA18962.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.252+21484C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111175475 | ||||||
| chr13:111175574
|
G | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | NA18957.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.252+21583G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111175574 | ||||||
| chr13:111175937
|
C | T | 1 | a0001c0001t0004g0241 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.252+21946C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111175937 | ||||||
| chr13:111175968
|
A | C | 1 | a0001c0001t0029g0201 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.252+21977A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111175968 | ||||||
| chr13:111176010
|
G | C | 1 | a0004c0017t0003g0120 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.252+22019G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111176010 | ||||||
| chr13:111176030
|
A | G | 14 | a0001c0001t0001g0113a0001c0001t0001g0253a0001c0001t0003g0128others(11): Show | 14 | HG01071.hp1 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.252+22039A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111176030 | ||||||
| chr13:111176041
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0177 | 2 | HG01099.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.252+22050C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111176041 | ||||||
| chr13:111176099
|
T | C | 9 | a0001c0001t0003g0024a0001c0001t0007g0094a0001c0001t0012g0001others(6): Show | 9 | HG01192.hp1 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.252+22108T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111176099 | ||||||
| chr13:111176135
|
A | G | 14 | a0001c0001t0001g0113a0001c0001t0001g0253a0001c0001t0003g0128others(11): Show | 14 | HG01071.hp1 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.252+22144A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111176135 | ||||||
| chr13:111176270
|
G | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(268): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.252+22279G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111176270 | ||||||
| chr13:111176368
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.252+22377C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111176368 | ||||||
| chr13:111176665
|
C | T | 52 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0006g0246others(49): Show | 52 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.252+22674C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111176665 | ||||||
| chr13:111176708
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.252+22717G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111176708 | ||||||
| chr13:111176814
|
T | A | 1 | a0001c0001t0001g0050 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.252+22823T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111176814 | ||||||
| chr13:111177052
|
C | T | 51 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0015g0272others(48): Show | 51 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.252+23061C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111177052 | ||||||
| chr13:111177311
|
A | C | 235 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.252+23320A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111177311 | ||||||
| chr13:111177465
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.252+23474C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111177465 | ||||||
| chr13:111177771
|
C | T | 8 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(5): Show | 8 | HG02559.hp1 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.252+23780C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111177771 | ||||||
| chr13:111177772
|
G | C | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.252+23781G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111177772 | ||||||
| chr13:111177839
|
T | TA | 17 | a0001c0001t0001g0051a0001c0001t0001g0113a0001c0001t0001g0253others(14): Show | 17 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.252+23850dupA | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111177839 | |||||
| chr13:111177949
|
C | T | 2 | a0001c0001t0002g0011a0001c0001t0016g0012 | 2 | HG02895.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.252+23958C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111177949 | ||||||
| chr13:111178328
|
G | A | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.252+24337G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111178328 | ||||||
| chr13:111178361
|
G | A | 54 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0129others(51): Show | 54 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.252+24370G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111178361 | ||||||
| chr13:111178628
|
C | T | 1 | a0001c0005t0020g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.252+24637C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111178628 | ||||||
| chr13:111178638
|
C | T | 1 | a0001c0001t0003g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.252+24647C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111178638 | ||||||
| chr13:111178711
|
G | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.252+24720G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111178711 | ||||||
| chr13:111178850
|
G | T | 1 | a0001c0001t0003g0024 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.252+24859G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111178850 | ||||||
| chr13:111178928
|
C | T | 1 | a0001c0016t0008g0227 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.252+24937C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111178928 | ||||||
| chr13:111179078
|
G | GT | 4 | a0001c0001t0001g0097a0001c0001t0001g0220a0001c0001t0004g0045others(1): Show | 4 | HG00140.hp2 HG02738.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+25089dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111179078 | |||||
| chr13:111179078
|
G | GTTTC | 208 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.252+25089_252+2509 others(8): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111179078 | |||||
| chr13:111179080
|
T | TTCTTC | 4 | a0001c0001t0001g0051a0001c0001t0002g0099a0001c0001t0012g0001others(1): Show | 4 | HG01169.hp1 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+25089_252+2509 others(9): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111179080 | ||||||
| chr13:111179081
|
C | T | 4 | a0001c0001t0001g0051a0001c0001t0002g0099a0001c0001t0012g0001others(1): Show | 4 | HG01169.hp1 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+25090C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111179081 | ||||||
| chr13:111179324
|
T | G | 2 | a0001c0001t0006g0032a0001c0001t0006g0083 | 2 | HG00558.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.252+25333T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111179324 | ||||||
| chr13:111179487
|
A | G | 58 | a0001c0001t0003g0104a0001c0001t0003g0108a0001c0001t0003g0145others(55): Show | 58 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.252+25496A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111179487 | ||||||
| chr13:111179542
|
G | A | 16 | a0001c0001t0003g0107a0001c0001t0003g0119a0001c0001t0003g0136others(13): Show | 16 | HG00140.hp1 HG00738.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.252+25551G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111179542 | ||||||
| chr13:111179566
|
T | C | 76 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(73): Show | 76 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.252+25575T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111179566 | ||||||
| chr13:111180170
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0012g0013 | 2 | HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.253-25119C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111180170 | ||||||
| chr13:111180263
|
T | C | 1 | a0001c0002t0002g0237 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.253-25026T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111180263 | ||||||
| chr13:111180286
|
C | T | 9 | a0001c0001t0003g0024a0001c0001t0007g0094a0001c0001t0008g0003others(6): Show | 9 | HG02559.hp1 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-25003C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111180286 | ||||||
| chr13:111180363
|
T | C | 5 | a0001c0001t0002g0099a0001c0003t0001g0142a0001c0003t0003g0021others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.253-24926T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111180363 | ||||||
| chr13:111180410
|
C | G | 1 | a0001c0001t0006g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.253-24879C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111180410 | ||||||
| chr13:111180443
|
C | T | 1 | a0001c0002t0002g0060 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.253-24846C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111180443 | ||||||
| chr13:111180579
|
T | A | 1 | a0001c0001t0001g0200 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.253-24710T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111180579 | ||||||
| chr13:111180600
|
G | C | 1 | a0001c0001t0001g0066 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.253-24689G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111180600 | ||||||
| chr13:111180662
|
G | A | 1 | a0001c0005t0020g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.253-24627G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111180662 | ||||||
| chr13:111180956
|
C | G | 1 | a0001c0001t0001g0195 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.253-24333C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111180956 | ||||||
| chr13:111181192
|
A | T | 1 | a0001c0001t0001g0051 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.253-24097A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111181192 | ||||||
| chr13:111181265
|
G | A | 1 | a0001c0001t0003g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.253-24024G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111181265 | ||||||
| chr13:111181274
|
T | G | 88 | a0001c0001t0001g0005a0001c0001t0001g0048a0001c0001t0001g0051others(85): Show | 88 | HG00280.hp2 HG00323.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.253-24015T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111181274 | ||||||
| chr13:111181299
|
A | C | 4 | a0001c0001t0003g0178a0001c0001t0003g0216a0001c0001t0003g0262others(1): Show | 4 | HG00140.hp1 HG01099.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-23990A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111181299 | ||||||
| chr13:111181381
|
A | T | 2 | a0001c0001t0016g0077a0001c0012t0030g0072 | 2 | HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.253-23908A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111181381 | ||||||
| chr13:111181601
|
C | G | 9 | a0001c0001t0006g0041a0001c0001t0009g0171a0001c0001t0009g0202others(6): Show | 9 | NA18941.hp2 NA18962.hp2 NA18982.hp1 others(6): Show |
intron_variant | MODIFIER | c.253-23688C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111181601 | ||||||
| chr13:111181635
|
G | T | 1 | a0001c0001t0001g0135 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.253-23654G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111181635 | ||||||
| chr13:111181684
|
A | G | 110 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(107): Show | 110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.253-23605A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111181684 | ||||||
| chr13:111181748
|
G | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(107): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.253-23541G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111181748 | ||||||
| chr13:111181780
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.253-23509G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111181780 | ||||||
| chr13:111181814
|
A | G | 3 | a0001c0002t0002g0079a0001c0002t0002g0150a0001c0002t0002g0165 | 3 | HG02015.hp1 HG02132.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.253-23475A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111181814 | ||||||
| chr13:111181840
|
C | T | 10 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0011g0006others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.253-23449C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111181840 | ||||||
| chr13:111181962
|
T | A | 2 | a0001c0003t0003g0021a0001c0003t0003g0146 | 2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.253-23327T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111181962 | ||||||
| chr13:111182109
|
T | C | 9 | a0001c0001t0003g0024a0001c0001t0007g0094a0001c0001t0008g0003others(6): Show | 9 | HG02559.hp1 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-23180T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111182109 | ||||||
| chr13:111182180
|
C | T | 2 | a0001c0001t0007g0028a0001c0001t0007g0132 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.253-23109C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111182180 | ||||||
| chr13:111182181
|
G | A | 6 | a0001c0001t0006g0263a0001c0001t0013g0154a0001c0001t0013g0162others(3): Show | 6 | HG00642.hp1 HG01928.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-23108G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111182181 | ||||||
| chr13:111182432
|
G | A | 2 | a0001c0002t0002g0082a0001c0002t0002g0157 | 2 | NA18979.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.253-22857G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111182432 | ||||||
| chr13:111182548
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(4): Show | 7 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.253-22741G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111182548 | ||||||
| chr13:111182573
|
C | T | 1 | a0001c0001t0019g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.253-22716C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111182573 | ||||||
| chr13:111182591
|
G | T | 1 | a0001c0002t0002g0265 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.253-22698G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111182591 | ||||||
| chr13:111182676
|
C | T | 1 | a0001c0005t0020g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.253-22613C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111182676 | ||||||
| chr13:111182895
|
A | G | 1 | a0001c0001t0007g0009 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.253-22394A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111182895 | ||||||
| chr13:111182917
|
A | G | 2 | a0001c0001t0003g0025a0001c0001t0004g0122 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.253-22372A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111182917 | ||||||
| chr13:111183072
|
G | C | 1 | a0001c0001t0001g0137 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.253-22217G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111183072 | ||||||
| chr13:111183128
|
G | C | 1 | a0001c0002t0002g0237 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.253-22161G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111183128 | ||||||
| chr13:111183189
|
G | A | 1 | a0001c0005t0020g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.253-22100G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111183189 | ||||||
| chr13:111183235
|
G | A | 1 | a0001c0001t0005g0114 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.253-22054G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111183235 | ||||||
| chr13:111183343
|
C | CT | 29 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(26): Show | 29 | HG00558.hp2 HG00642.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.253-21934dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111183343 | |||||
| chr13:111183353
|
T | A | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.253-21936T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111183353 | ||||||
| chr13:111183567
|
A | G | 1 | a0001c0015t0002g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.253-21722A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111183567 | ||||||
| chr13:111183936
|
C | T | 2 | a0001c0001t0015g0271a0001c0001t0015g0273 | 2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.253-21353C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111183936 | ||||||
| chr13:111184090
|
G | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0096 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.253-21199G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111184090 | ||||||
| chr13:111184101
|
C | T | 4 | a0001c0002t0010g0080a0001c0002t0010g0081a0001c0002t0010g0159others(1): Show | 4 | NA18968.hp2 NA18999.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-21188C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111184101 | ||||||
| chr13:111184105
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.253-21184G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111184105 | ||||||
| chr13:111184359
|
G | A | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.253-20930G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111184359 | ||||||
| chr13:111184360
|
T | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.253-20929T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111184360 | ||||||
| chr13:111184507
|
C | G | 1 | a0001c0015t0002g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.253-20782C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111184507 | ||||||
| chr13:111184517
|
C | T | 1 | a0001c0007t0004g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.253-20772C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111184517 | ||||||
| chr13:111184752
|
G | A | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.253-20537G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111184752 | ||||||
| chr13:111184808
|
C | T | 16 | a0001c0001t0001g0160a0001c0001t0006g0032a0001c0001t0006g0041others(13): Show | 16 | HG00558.hp2 HG00642.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.253-20481C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111184808 | ||||||
| chr13:111184913
|
T | G | 37 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(34): Show | 37 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.253-20376T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111184913 | ||||||
| chr13:111185010
|
A | AT | 8 | a0001c0001t0003g0213a0001c0001t0009g0171a0001c0001t0009g0202others(5): Show | 8 | HG02135.hp1 NA18962.hp2 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.253-20268dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111185010 | |||||
| chr13:111185015
|
T | G | 4 | a0001c0001t0003g0119a0001c0001t0018g0020a0001c0001t0018g0038others(1): Show | 4 | HG00738.hp1 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-20274T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111185015 | ||||||
| chr13:111185066
|
T | C | 5 | a0001c0001t0002g0099a0001c0003t0001g0142a0001c0003t0003g0021others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.253-20223T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111185066 | ||||||
| chr13:111185076
|
G | T | 1 | a0001c0001t0003g0087 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.253-20213G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111185076 | ||||||
| chr13:111185122
|
C | T | 3 | a0001c0001t0006g0032a0001c0001t0006g0218a0001c0001t0006g0234 | 3 | HG00558.hp2 NA18950.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.253-20167C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111185122 | ||||||
| chr13:111185190
|
A | G | 40 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.253-20099A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111185190 | ||||||
| chr13:111185212
|
G | C | 9 | a0001c0001t0006g0083a0001c0001t0009g0171a0001c0001t0009g0202others(6): Show | 9 | NA18939.hp1 NA18941.hp2 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-20077G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111185212 | ||||||
| chr13:111185258
|
C | T | 2 | a0001c0001t0001g0040a0001c0002t0002g0031 | 2 | NA18952.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.253-20031C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111185258 | ||||||
| chr13:111185372
|
C | T | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.253-19917C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111185372 | ||||||
| chr13:111185564
|
G | A | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.253-19725G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111185564 | ||||||
| chr13:111185760
|
G | T | 5 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0004g0045others(2): Show | 5 | NA18939.hp2 NA18986.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-19529G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111185760 | ||||||
| chr13:111185961
|
C | CGT | 53 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0137others(50): Show | 53 | HG00323.hp2 HG01099.hp2 HG01167.hp2 others(50): Show |
intron_variant | MODIFIER | c.253-19285_253-1928 others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111185961 | |||||
| chr13:111185961
|
C | CGTGT | 61 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0040others(58): Show | 61 | HG00280.hp2 HG00323.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.253-19287_253-1928 others(8): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111185961 | |||||
| chr13:111185961
|
C | CGTGTGT | 18 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0019others(15): Show | 18 | HG00280.hp1 HG00738.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.253-19289_253-1928 others(10): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111185961 | |||||
| chr13:111185961
|
C | CGTGTGTG others(1): Show |
15 | a0001c0001t0001g0052a0001c0001t0001g0084a0001c0001t0001g0129others(12): Show | 15 | HG00597.hp2 HG01361.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.253-19291_253-1928 others(12): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111185961 | |||||
| chr13:111185961
|
C | CGTGTGTG others(3): Show |
16 | a0001c0001t0001g0016a0001c0001t0001g0043a0001c0001t0001g0051others(13): Show | 16 | HG00099.hp2 HG00639.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.253-19293_253-1928 others(14): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111185961 | |||||
| chr13:111185961
|
C | CGTGTGTG others(5): Show |
3 | a0001c0001t0001g0188a0001c0001t0005g0114a0001c0001t0005g0230 | 3 | HG01071.hp1 HG01081.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.253-19295_253-1928 others(16): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111185961 | |||||
| chr13:111185961
|
C | CGTGTGTG others(7): Show |
1 | a0001c0001t0001g0044 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.253-19297_253-1928 others(18): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111185961 | |||||
| chr13:111185961
|
CGT | C | 17 | a0001c0001t0003g0087a0001c0001t0003g0178a0001c0001t0003g0213others(14): Show | 17 | HG00140.hp1 HG01099.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.253-19285_253-1928 others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111185961 | |||||
| chr13:111185961
|
CGTGT | C | 15 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0088others(12): Show | 15 | HG00597.hp1 HG00642.hp2 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.253-19287_253-1928 others(8): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111185961 | |||||
| chr13:111185961
|
CGTGTGT | C | 8 | a0001c0001t0001g0138a0001c0001t0004g0244a0001c0001t0006g0032others(5): Show | 8 | HG00558.hp2 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.253-19289_253-1928 others(10): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111185961 | |||||
| chr13:111185961
|
CGTGTGTG others(1): Show |
C | 16 | a0001c0001t0001g0160a0001c0001t0002g0099a0001c0001t0006g0041others(13): Show | 16 | HG00642.hp1 HG00741.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.253-19291_253-1928 others(12): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111185961 | |||||
| chr13:111185961
|
CGTGTGTG others(3): Show |
C | 8 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0003g0025others(5): Show | 8 | HG01109.hp1 HG01192.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.253-19293_253-1928 others(14): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111185961 | |||||
| chr13:111185961
|
CGTGTGTG others(9): Show |
C | 3 | a0001c0001t0001g0217a0001c0008t0001g0098a0001c0008t0001g0109 | 3 | HG01069.hp1 HG01071.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.253-19299_253-1928 others(20): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111185961 | |||||
| chr13:111186010
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.253-19279G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111186010 | ||||||
| chr13:111186384
|
GAAAT | G | 28 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(25): Show | 28 | HG00140.hp1 HG00597.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.253-18900_253-1889 others(8): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111186384 | |||||
| chr13:111186483
|
A | T | 1 | a0001c0001t0018g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.253-18806A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111186483 | ||||||
| chr13:111186745
|
T | C | 270 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.253-18544T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111186745 | ||||||
| chr13:111186823
|
C | G | 1 | a0003c0011t0005g0191 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.253-18466C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111186823 | ||||||
| chr13:111186889
|
A | C | 1 | a0001c0001t0011g0055 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.253-18400A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111186889 | ||||||
| chr13:111186934
|
G | A | 10 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0011g0006others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.253-18355G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111186934 | ||||||
| chr13:111186999
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0002t0002g0198 | 3 | HG01515.hp1 HG03492.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.253-18290T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111186999 | ||||||
| chr13:111187038
|
G | A | 1 | a0001c0001t0003g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.253-18251G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111187038 | ||||||
| chr13:111187101
|
G | A | 64 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0104others(61): Show | 64 | HG00099.hp2 HG00323.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.253-18188G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111187101 | ||||||
| chr13:111187131
|
G | A | 229 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.253-18158G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111187131 | ||||||
| chr13:111187392
|
T | C | 1 | a0001c0002t0002g0079 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.253-17897T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111187392 | ||||||
| chr13:111187464
|
A | G | 9 | a0001c0001t0003g0024a0001c0001t0007g0094a0001c0001t0008g0003others(6): Show | 9 | HG02559.hp1 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-17825A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111187464 | ||||||
| chr13:111187524
|
G | A | 2 | a0001c0001t0005g0102a0001c0001t0005g0103 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.253-17765G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111187524 | ||||||
| chr13:111187565
|
A | T | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.253-17724A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111187565 | ||||||
| chr13:111187729
|
A | T | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.253-17560A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111187729 | ||||||
| chr13:111187737
|
C | A | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.253-17552C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111187737 | ||||||
| chr13:111187986
|
T | G | 1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.253-17303T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111187986 | ||||||
| chr13:111188353
|
T | G | 1 | a0004c0017t0003g0120 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.253-16936T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111188353 | ||||||
| chr13:111188503
|
C | A | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.253-16786C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111188503 | ||||||
| chr13:111188517
|
C | T | 1 | a0001c0001t0032g0030 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.253-16772C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111188517 | ||||||
| chr13:111188612
|
ACAG | A | 9 | a0001c0001t0003g0024a0001c0001t0007g0094a0001c0001t0008g0003others(6): Show | 9 | HG02559.hp1 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-16672_253-1667 others(7): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111188612 | |||||
| chr13:111188853
|
G | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0188 | 2 | HG01109.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.253-16436G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111188853 | ||||||
| chr13:111188995
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.253-16294C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111188995 | ||||||
| chr13:111189102
|
G | A | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-16187G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111189102 | ||||||
| chr13:111189111
|
A | G | 1 | a0001c0001t0004g0241 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.253-16178A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111189111 | ||||||
| chr13:111189226
|
G | T | 1 | a0007c0010t0001g0095 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.253-16063G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111189226 | ||||||
| chr13:111189248
|
T | C | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-16041T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111189248 | ||||||
| chr13:111189285
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.253-16004G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111189285 | ||||||
| chr13:111189397
|
G | T | 1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.253-15892G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111189397 | ||||||
| chr13:111189517
|
C | T | 1 | a0001c0001t0003g0024 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.253-15772C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111189517 | ||||||
| chr13:111189684
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0066others(6): Show | 9 | HG02647.hp2 HG03195.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-15605C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111189684 | ||||||
| chr13:111189706
|
C | T | 12 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(9): Show | 12 | HG01071.hp1 HG01167.hp1 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.253-15583C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111189706 | ||||||
| chr13:111189821
|
G | A | 1 | a0001c0002t0002g0151 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.253-15468G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111189821 | ||||||
| chr13:111189833
|
TTTTAGCT others(5): Show |
T | 4 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0241others(1): Show | 4 | HG00738.hp2 HG02135.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-15455_253-1544 others(16): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111189833 | ||||||
| chr13:111189842
|
G | C | 1 | a0001c0001t0001g0048 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.253-15447G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111189842 | ||||||
| chr13:111189942
|
A | G | 2 | a0001c0007t0004g0059a0001c0007t0027g0054 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.253-15347A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111189942 | ||||||
| chr13:111190088
|
A | G | 1 | a0001c0001t0004g0045 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.253-15201A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111190088 | ||||||
| chr13:111190126
|
T | C | 1 | a0006c0019t0002g0175 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.253-15163T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111190126 | ||||||
| chr13:111190255
|
G | A | 5 | a0001c0001t0002g0099a0001c0003t0001g0142a0001c0003t0003g0021others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.253-15034G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111190255 | ||||||
| chr13:111190388
|
G | T | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.253-14901G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111190388 | ||||||
| chr13:111190420
|
A | G | 1 | a0001c0001t0003g0215 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.253-14869A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111190420 | ||||||
| chr13:111190441
|
T | A | 1 | a0001c0015t0002g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.253-14848T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111190441 | ||||||
| chr13:111190571
|
G | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.253-14718G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111190571 | ||||||
| chr13:111190597
|
T | C | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.253-14692T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111190597 | ||||||
| chr13:111190660
|
G | A | 61 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.253-14629G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111190660 | ||||||
| chr13:111190786
|
C | T | 1 | a0001c0002t0002g0157 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.253-14503C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111190786 | ||||||
| chr13:111190787
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.253-14502G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111190787 | ||||||
| chr13:111190910
|
C | G | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-14379C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111190910 | ||||||
| chr13:111191011
|
T | C | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-14278T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111191011 | ||||||
| chr13:111191030
|
G | C | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.253-14259G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111191030 | ||||||
| chr13:111191096
|
G | C | 2 | a0001c0001t0003g0104a0001c0001t0003g0108 | 2 | HG00099.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.253-14193G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111191096 | ||||||
| chr13:111191137
|
G | C | 9 | a0001c0001t0003g0024a0001c0001t0007g0094a0001c0001t0008g0003others(6): Show | 9 | HG02559.hp1 HG02809.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-14152G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111191137 | ||||||
| chr13:111191187
|
G | A | 3 | a0001c0001t0003g0107a0001c0001t0003g0136a0001c0001t0003g0215 | 3 | HG01891.hp2 HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.253-14102G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111191187 | ||||||
| chr13:111191201
|
G | A | 1 | a0001c0001t0003g0119 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.253-14088G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111191201 | ||||||
| chr13:111191224
|
A | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.253-14065A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111191224 | ||||||
| chr13:111191282
|
C | T | 2 | a0001c0001t0007g0028a0001c0001t0007g0132 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.253-14007C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111191282 | ||||||
| chr13:111191471
|
G | A | 5 | a0001c0001t0001g0068a0001c0001t0004g0064a0001c0001t0004g0065others(2): Show | 5 | HG01167.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.253-13818G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111191471 | ||||||
| chr13:111191535
|
G | T | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-13754G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111191535 | ||||||
| chr13:111191616
|
A | C | 1 | a0001c0001t0005g0063 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.253-13673A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111191616 | ||||||
| chr13:111191766
|
A | G | 1 | a0001c0001t0025g0176 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.253-13523A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111191766 | ||||||
| chr13:111191832
|
T | C | 1 | a0001c0001t0004g0064 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.253-13457T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111191832 | ||||||
| chr13:111191912
|
C | T | 1 | a0001c0001t0004g0110 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.253-13377C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111191912 | ||||||
| chr13:111191918
|
A | G | 120 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(117): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.253-13371A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111191918 | ||||||
| chr13:111191949
|
A | G | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.253-13340A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111191949 | ||||||
| chr13:111192181
|
C | T | 1 | a0001c0004t0022g0209 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.253-13108C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192181 | ||||||
| chr13:111192196
|
C | T | 2 | a0001c0001t0018g0020a0001c0001t0018g0038 | 2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.253-13093C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192196 | ||||||
| chr13:111192232
|
A | G | 24 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(21): Show | 24 | HG00099.hp2 HG00597.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.253-13057A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192232 | ||||||
| chr13:111192307
|
C | G | 1 | a0001c0001t0006g0263 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.253-12982C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192307 | ||||||
| chr13:111192348
|
A | G | 1 | a0001c0001t0009g0250 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.253-12941A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192348 | ||||||
| chr13:111192507
|
T | C | 1 | a0001c0001t0011g0055 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.253-12782T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192507 | ||||||
| chr13:111192653
|
G | A | 5 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017others(2): Show | 5 | HG01109.hp1 HG01192.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-12636G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192653 | ||||||
| chr13:111192720
|
G | A | 273 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.253-12569G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192720 | ||||||
| chr13:111192721
|
G | T | 273 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.253-12568G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192721 | ||||||
| chr13:111192722
|
G | T | 273 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.253-12567G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192722 | ||||||
| chr13:111192723
|
T | C | 273 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.253-12566T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192723 | ||||||
| chr13:111192724
|
A | C | 273 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.253-12565A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192724 | ||||||
| chr13:111192726
|
C | T | 273 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.253-12563C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192726 | ||||||
| chr13:111192736
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.253-12553C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192736 | ||||||
| chr13:111192841
|
T | C | 6 | a0001c0001t0006g0263a0001c0001t0013g0154a0001c0001t0013g0162others(3): Show | 6 | HG00642.hp1 HG01928.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-12448T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192841 | ||||||
| chr13:111192848
|
A | G | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.253-12441A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192848 | ||||||
| chr13:111192881
|
AACAC | A | 2 | a0002c0009t0002g0069a0002c0009t0002g0112 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.253-12403_253-1240 others(8): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111192881 | |||||
| chr13:111192884
|
A | G | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.253-12405A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192884 | ||||||
| chr13:111192923
|
A | T | 1 | a0001c0001t0012g0001 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.253-12366A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192923 | ||||||
| chr13:111192953
|
G | A | 14 | a0001c0001t0001g0160a0001c0001t0006g0032a0001c0001t0006g0041others(11): Show | 14 | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.253-12336G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192953 | ||||||
| chr13:111192995
|
A | G | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.253-12294A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111192995 | ||||||
| chr13:111193047
|
C | T | 4 | a0001c0002t0010g0080a0001c0002t0010g0081a0001c0002t0010g0159others(1): Show | 4 | NA18968.hp2 NA18999.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-12242C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111193047 | ||||||
| chr13:111193220
|
A | G | 6 | a0001c0001t0016g0143a0001c0001t0019g0071a0001c0003t0001g0142others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-12069A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111193220 | ||||||
| chr13:111193291
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.253-11998T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111193291 | ||||||
| chr13:111193342
|
C | G | 2 | a0001c0001t0007g0028a0001c0001t0007g0132 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.253-11947C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111193342 | ||||||
| chr13:111193371
|
C | T | 1 | a0001c0001t0034g0061 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.253-11918C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111193371 | ||||||
| chr13:111193446
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.253-11843C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111193446 | ||||||
| chr13:111193494
|
G | A | 1 | a0001c0002t0002g0169 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.253-11795G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111193494 | ||||||
| chr13:111193631
|
G | A | 1 | a0001c0002t0002g0190 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.253-11658G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111193631 | ||||||
| chr13:111193686
|
A | G | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.253-11603A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111193686 | ||||||
| chr13:111193698
|
C | T | 1 | a0001c0001t0003g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.253-11591C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111193698 | ||||||
| chr13:111193699
|
G | A | 1 | a0001c0001t0005g0212 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.253-11590G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111193699 | ||||||
| chr13:111193912
|
G | A | 16 | a0001c0001t0001g0160a0001c0001t0006g0032a0001c0001t0006g0041others(13): Show | 16 | HG00558.hp2 HG00642.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.253-11377G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111193912 | ||||||
| chr13:111193924
|
A | C | 18 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(15): Show | 18 | HG00597.hp1 HG01891.hp2 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.253-11365A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111193924 | ||||||
| chr13:111194004
|
T | C | 9 | a0001c0001t0006g0083a0001c0001t0009g0171a0001c0001t0009g0202others(6): Show | 9 | NA18939.hp1 NA18941.hp2 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.253-11285T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111194004 | ||||||
| chr13:111194088
|
C | T | 29 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(26): Show | 29 | HG00140.hp1 HG00597.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.253-11201C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111194088 | ||||||
| chr13:111194092
|
G | A | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.253-11197G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111194092 | ||||||
| chr13:111194160
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.253-11129C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111194160 | ||||||
| chr13:111194209
|
C | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0177 | 2 | HG01099.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.253-11080C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111194209 | ||||||
| chr13:111194262
|
A | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.253-11027A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111194262 | ||||||
| chr13:111194281
|
T | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.253-11008T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111194281 | ||||||
| chr13:111194372
|
A | C | 1 | a0001c0001t0009g0214 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.253-10917A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111194372 | ||||||
| chr13:111194392
|
C | T | 2 | a0001c0001t0003g0025a0001c0001t0004g0122 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.253-10897C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111194392 | ||||||
| chr13:111194398
|
A | T | 1 | a0001c0005t0020g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.253-10891A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111194398 | ||||||
| chr13:111194771
|
T | C | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.253-10518T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111194771 | ||||||
| chr13:111194800
|
A | G | 2 | a0001c0001t0015g0271a0001c0001t0015g0273 | 2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.253-10489A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111194800 | ||||||
| chr13:111194872
|
TCCTTGAG others(4): Show |
T | 8 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(5): Show | 8 | HG02559.hp1 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.253-10416_253-1040 others(15): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111194872 | ||||||
| chr13:111194988
|
G | T | 1 | a0001c0001t0016g0143 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.253-10301G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111194988 | ||||||
| chr13:111195010
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.253-10279C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111195010 | ||||||
| chr13:111195084
|
C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(92): Show | 95 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.253-10205C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111195084 | ||||||
| chr13:111195088
|
T | C | 6 | a0001c0001t0016g0143a0001c0001t0019g0071a0001c0003t0001g0142others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-10201T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111195088 | ||||||
| chr13:111195294
|
C | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(59): Show | 62 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.253-9995C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111195294 | ||||||
| chr13:111195490
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.253-9799C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111195490 | ||||||
| chr13:111195617
|
G | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.253-9672G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111195617 | ||||||
| chr13:111195706
|
C | T | 1 | a0001c0001t0003g0215 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.253-9583C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111195706 | ||||||
| chr13:111195810
|
T | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.253-9479T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111195810 | ||||||
| chr13:111195867
|
A | G | 96 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.253-9422A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111195867 | ||||||
| chr13:111195870
|
G | A | 6 | a0001c0001t0006g0263a0001c0001t0013g0154a0001c0001t0013g0162others(3): Show | 6 | HG00642.hp1 HG01928.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-9419G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111195870 | ||||||
| chr13:111196073
|
G | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.253-9216G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111196073 | ||||||
| chr13:111196141
|
C | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.253-9148C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111196141 | ||||||
| chr13:111196157
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.253-9132G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111196157 | ||||||
| chr13:111196163
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.253-9126C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111196163 | ||||||
| chr13:111196323
|
C | T | 32 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(29): Show | 32 | HG00140.hp1 HG00597.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.253-8966C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111196323 | ||||||
| chr13:111196369
|
A | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.253-8920A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111196369 | ||||||
| chr13:111196426
|
A | G | 6 | a0001c0001t0016g0143a0001c0001t0019g0071a0001c0003t0001g0142others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.253-8863A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111196426 | ||||||
| chr13:111196426
|
A | T | 1 | a0001c0001t0017g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.253-8863A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111196426 | ||||||
| chr13:111196486
|
G | A | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.253-8803G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111196486 | ||||||
| chr13:111196742
|
TAAGCTGA others(27): Show |
T | 87 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(84): Show | 87 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.253-8541_253-8508d others(36): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111196742 | |||||
| chr13:111196867
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.253-8422G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111196867 | ||||||
| chr13:111196878
|
T | C | 6 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017others(3): Show | 6 | HG01109.hp1 HG01192.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.253-8411T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111196878 | ||||||
| chr13:111196994
|
T | C | 87 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(84): Show | 87 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.253-8295T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111196994 | ||||||
| chr13:111197140
|
C | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.253-8149C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111197140 | ||||||
| chr13:111197206
|
G | C | 87 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(84): Show | 87 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.253-8083G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111197206 | ||||||
| chr13:111197254
|
C | G | 1 | a0001c0001t0008g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.253-8035C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111197254 | ||||||
| chr13:111197254
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.253-8035C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111197254 | ||||||
| chr13:111197283
|
C | T | 206 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(203): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.253-8006C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111197283 | ||||||
| chr13:111197289
|
C | T | 1 | a0001c0001t0004g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.253-8000C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111197289 | ||||||
| chr13:111197386
|
G | T | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.253-7903G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111197386 | ||||||
| chr13:111197532
|
T | C | 1 | a0001c0002t0002g0203 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.253-7757T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111197532 | ||||||
| chr13:111197976
|
A | C | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.253-7313A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111197976 | ||||||
| chr13:111198086
|
G | T | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.253-7203G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111198086 | ||||||
| chr13:111198099
|
G | C | 88 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(85): Show | 88 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.253-7190G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111198099 | ||||||
| chr13:111198140
|
G | T | 5 | a0001c0002t0002g0031a0001c0002t0002g0151a0001c0002t0002g0152others(2): Show | 5 | NA18941.hp1 NA18955.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-7149G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111198140 | ||||||
| chr13:111198192
|
T | C | 109 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.253-7097T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111198192 | ||||||
| chr13:111198241
|
G | A | 1 | a0001c0001t0003g0274 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.253-7048G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111198241 | ||||||
| chr13:111198249
|
C | T | 1 | a0001c0001t0007g0094 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.253-7040C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111198249 | ||||||
| chr13:111198285
|
C | T | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.253-7004C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111198285 | ||||||
| chr13:111198323
|
C | T | 44 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(41): Show | 44 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.253-6966C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111198323 | ||||||
| chr13:111198338
|
A | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.253-6951A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111198338 | ||||||
| chr13:111198352
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.253-6937C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111198352 | ||||||
| chr13:111198457
|
G | A | 3 | a0001c0001t0011g0006a0001c0001t0011g0007a0001c0001t0011g0075 | 3 | HG01884.hp1 HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.253-6832G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111198457 | ||||||
| chr13:111198513
|
C | T | 1 | a0001c0001t0004g0045 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.253-6776C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111198513 | ||||||
| chr13:111198619
|
T | C | 3 | a0001c0001t0004g0242a0001c0001t0004g0243a0001c0001t0006g0246 | 3 | NA18968.hp1 NA18971.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.253-6670T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111198619 | ||||||
| chr13:111198910
|
CA | C | 62 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(59): Show | 62 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.253-6378delA | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111198910 | ||||||
| chr13:111198968
|
C | T | 1 | a0001c0001t0003g0184 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.253-6321C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111198968 | ||||||
| chr13:111198981
|
T | C | 5 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017others(2): Show | 5 | HG01109.hp1 HG01192.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.253-6308T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111198981 | ||||||
| chr13:111199154
|
C | T | 76 | a0001c0001t0001g0019a0001c0001t0001g0129a0001c0001t0001g0137others(73): Show | 76 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.253-6135C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111199154 | ||||||
| chr13:111199355
|
GC | G | 10 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0011g0006others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.253-5932delC | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111199355 | |||||
| chr13:111199455
|
A | G | 2 | a0001c0001t0007g0028a0001c0001t0007g0132 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.253-5834A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111199455 | ||||||
| chr13:111199665
|
G | T | 1 | a0001c0001t0007g0094 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.253-5624G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111199665 | ||||||
| chr13:111200060
|
C | T | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18941.hp2 NA18962.hp2 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.253-5229C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111200060 | ||||||
| chr13:111200121
|
T | C | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.253-5168T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111200121 | ||||||
| chr13:111200155
|
G | C | 17 | a0001c0001t0001g0160a0001c0001t0006g0032a0001c0001t0006g0041others(14): Show | 17 | HG00558.hp2 HG00642.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.253-5134G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111200155 | ||||||
| chr13:111200163
|
C | A | 8 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(5): Show | 8 | HG02559.hp1 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.253-5126C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111200163 | ||||||
| chr13:111200164
|
T | C | 6 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017others(3): Show | 6 | HG01109.hp1 HG01192.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.253-5125T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111200164 | ||||||
| chr13:111200165
|
T | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.253-5124T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111200165 | ||||||
| chr13:111200226
|
A | G | 1 | a0001c0002t0002g0152 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.253-5063A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111200226 | ||||||
| chr13:111200345
|
T | C | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.253-4944T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111200345 | ||||||
| chr13:111200453
|
C | CT | 48 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0025others(45): Show | 48 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.253-4823dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111200453 | |||||
| chr13:111200453
|
C | CTT | 63 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.253-4824_253-4823d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111200453 | |||||
| chr13:111200701
|
T | A | 202 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.253-4588T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111200701 | ||||||
| chr13:111200801
|
G | C | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18941.hp2 NA18962.hp2 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.253-4488G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111200801 | ||||||
| chr13:111200920
|
A | G | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.253-4369A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111200920 | ||||||
| chr13:111201009
|
A | G | 10 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0011g0006others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.253-4280A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111201009 | ||||||
| chr13:111201018
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.253-4271G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111201018 | ||||||
| chr13:111201180
|
C | T | 1 | a0001c0002t0001g0170 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.253-4109C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111201180 | ||||||
| chr13:111201440
|
A | G | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.253-3849A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111201440 | ||||||
| chr13:111201519
|
A | T | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.253-3770A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111201519 | ||||||
| chr13:111201704
|
A | C | 75 | a0001c0001t0001g0005a0001c0001t0001g0040a0001c0001t0001g0068others(72): Show | 75 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.253-3585A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111201704 | ||||||
| chr13:111201846
|
C | T | 93 | a0001c0001t0001g0039a0001c0001t0001g0068a0001c0001t0001g0084others(90): Show | 93 | HG00280.hp2 HG00323.hp1 HG00642.hp1 others(90): Show |
intron_variant | MODIFIER | c.253-3443C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111201846 | ||||||
| chr13:111201856
|
C | G | 4 | a0001c0001t0002g0011a0001c0001t0016g0012a0001c0001t0018g0038others(1): Show | 4 | HG01192.hp1 HG02895.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.253-3433C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111201856 | ||||||
| chr13:111201865
|
C | T | 1 | a0001c0001t0003g0228 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.253-3424C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111201865 | ||||||
| chr13:111201876
|
G | A | 6 | a0001c0001t0009g0202a0001c0001t0009g0214a0001c0001t0009g0258others(3): Show | 6 | NA18941.hp2 NA18962.hp2 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.253-3413G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111201876 | ||||||
| chr13:111201962
|
A | G | 7 | a0001c0001t0009g0202a0001c0001t0009g0214a0001c0001t0009g0250others(4): Show | 7 | NA18941.hp2 NA18962.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.253-3327A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111201962 | ||||||
| chr13:111202059
|
C | T | 2 | a0001c0006t0012g0121a0001c0006t0012g0124 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.253-3230C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111202059 | ||||||
| chr13:111202149
|
G | A | 1 | a0001c0001t0012g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.253-3140G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111202149 | ||||||
| chr13:111202162
|
C | T | 1 | a0001c0001t0003g0087 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.253-3127C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111202162 | ||||||
| chr13:111202305
|
T | C | 1 | a0001c0001t0006g0234 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.253-2984T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111202305 | ||||||
| chr13:111202485
|
G | A | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.253-2804G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111202485 | ||||||
| chr13:111202570
|
C | A | 40 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.253-2719C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111202570 | ||||||
| chr13:111202622
|
C | T | 2 | a0001c0002t0002g0158a0001c0002t0002g0203 | 2 | NA18990.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.253-2667C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111202622 | ||||||
| chr13:111202867
|
G | A | 1 | a0001c0001t0003g0145 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.253-2422G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111202867 | ||||||
| chr13:111203090
|
T | C | 1 | a0001c0001t0009g0171 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.253-2199T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111203090 | ||||||
| chr13:111203329
|
A | T | 1 | a0001c0001t0001g0180 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.253-1960A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111203329 | ||||||
| chr13:111203336
|
A | G | 88 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(85): Show | 88 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.253-1953A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111203336 | ||||||
| chr13:111203349
|
G | A | 1 | a0001c0001t0002g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.253-1940G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111203349 | ||||||
| chr13:111203365
|
A | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.253-1924A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111203365 | ||||||
| chr13:111203563
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.253-1726G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111203563 | ||||||
| chr13:111203662
|
T | C | 1 | a0001c0001t0006g0218 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.253-1627T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111203662 | ||||||
| chr13:111203774
|
A | T | 1 | a0001c0001t0016g0077 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.253-1515A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111203774 | ||||||
| chr13:111203856
|
G | A | 1 | a0001c0001t0003g0089 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.253-1433G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111203856 | ||||||
| chr13:111203929
|
C | T | 19 | a0001c0001t0001g0040a0001c0001t0001g0047a0001c0001t0001g0049others(16): Show | 19 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.253-1360C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111203929 | ||||||
| chr13:111204169
|
G | A | 2 | a0001c0001t0003g0025a0001c0001t0004g0122 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.253-1120G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111204169 | ||||||
| chr13:111204251
|
G | A | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18941.hp2 NA18962.hp2 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.253-1038G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111204251 | ||||||
| chr13:111204253
|
C | G | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.253-1036C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111204253 | ||||||
| chr13:111204337
|
G | C | 17 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(14): Show | 17 | HG00558.hp2 HG00642.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.253-952G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111204337 | ||||||
| chr13:111204409
|
A | G | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.253-880A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111204409 | ||||||
| chr13:111204538
|
G | A | 54 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(51): Show | 54 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.253-751G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111204538 | ||||||
| chr13:111204722
|
A | G | 8 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(5): Show | 8 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.253-567A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111204722 | ||||||
| chr13:111204805
|
A | T | 1 | a0001c0013t0001g0100 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.253-484A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111204805 | ||||||
| chr13:111204809
|
A | G | 1 | a0001c0001t0003g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.253-480A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111204809 | ||||||
| chr13:111204966
|
G | GC | 39 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(36): Show | 39 | HG00140.hp1 HG00597.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.253-323_253-322ins others(1): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111204966 | ||||||
| chr13:111204985
|
C | T | 1 | a0001c0003t0019g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.253-304C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111204985 | ||||||
| chr13:111205002
|
A | ACCCCG | 41 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.253-277_253-273dup others(5): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr13 | 111205002 | |||||
| chr13:111205012
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.253-277G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111205012 | ||||||
| chr13:111205080
|
C | T | 2 | a0001c0001t0005g0063a0001c0001t0005g0126 | 2 | HG01175.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.253-209C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111205080 | ||||||
| chr13:111205081
|
G | A | 104 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.253-208G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 2/21 | chr13 | 111205081 | ||||||
| chr13:111205520
|
T | A | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18941.hp2 NA18962.hp2 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.337+147T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111205520 | ||||||
| chr13:111205641
|
T | G | 1 | a0001c0001t0033g0101 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.337+268T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111205641 | ||||||
| chr13:111205659
|
G | T | 2 | a0001c0002t0001g0170a0001c0002t0024g0183 | 2 | HG01257.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.337+286G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111205659 | ||||||
| chr13:111205756
|
T | C | 273 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.337+383T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111205756 | ||||||
| chr13:111205983
|
A | T | 1 | a0001c0001t0001g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.337+610A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111205983 | ||||||
| chr13:111206085
|
G | T | 235 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.337+712G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206085 | ||||||
| chr13:111206147
|
G | A | 4 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017others(1): Show | 4 | HG01109.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.337+774G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206147 | ||||||
| chr13:111206159
|
C | T | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.337+786C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206159 | ||||||
| chr13:111206199
|
C | T | 2 | a0002c0009t0002g0069a0002c0009t0002g0112 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.337+826C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206199 | ||||||
| chr13:111206232
|
GA | G | 3 | a0001c0002t0021g0255a0001c0002t0021g0256a0007c0010t0001g0095 | 3 | HG03486.hp2 NA18957.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.337+860delA | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206232 | ||||||
| chr13:111206235
|
G | A | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.337+862G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206235 | ||||||
| chr13:111206395
|
A | C | 18 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0097others(15): Show | 18 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.337+1022A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206395 | ||||||
| chr13:111206410
|
A | C | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.337+1037A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206410 | ||||||
| chr13:111206416
|
A | C | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.337+1043A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206416 | ||||||
| chr13:111206492
|
G | A | 5 | a0001c0001t0003g0145a0001c0001t0003g0179a0001c0001t0003g0210others(2): Show | 5 | HG02698.hp2 HG03669.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.337+1119G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206492 | ||||||
| chr13:111206507
|
C | A | 1 | a0001c0001t0004g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.337+1134C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206507 | ||||||
| chr13:111206562
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.337+1189A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206562 | ||||||
| chr13:111206564
|
G | A | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.337+1191G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206564 | ||||||
| chr13:111206593
|
T | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.337+1220T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206593 | ||||||
| chr13:111206605
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.337+1232C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206605 | ||||||
| chr13:111206727
|
C | T | 8 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(5): Show | 8 | HG02559.hp1 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.337+1354C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206727 | ||||||
| chr13:111206775
|
C | T | 1 | a0001c0001t0008g0003 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.337+1402C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206775 | ||||||
| chr13:111206789
|
G | A | 5 | a0001c0001t0002g0099a0001c0003t0001g0142a0001c0003t0003g0021others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.337+1416G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206789 | ||||||
| chr13:111206830
|
C | T | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.337+1457C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206830 | ||||||
| chr13:111206877
|
G | A | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.337+1504G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206877 | ||||||
| chr13:111206960
|
T | TAA | 19 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0084others(16): Show | 19 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.337+1601_337+1602d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr13 | 111206960 | |||||
| chr13:111206975
|
AG | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.337+1603delG | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206975 | ||||||
| chr13:111206976
|
G | A | 143 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0084others(140): Show | 143 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.337+1603G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111206976 | ||||||
| chr13:111207084
|
G | A | 211 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.337+1711G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111207084 | ||||||
| chr13:111207147
|
A | T | 5 | a0001c0001t0002g0099a0001c0003t0001g0142a0001c0003t0003g0021others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.337+1774A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111207147 | ||||||
| chr13:111207192
|
A | G | 2 | a0001c0001t0001g0105a0001c0001t0001g0131 | 2 | HG00280.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.337+1819A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111207192 | ||||||
| chr13:111207463
|
T | C | 108 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(105): Show | 108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.337+2090T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111207463 | ||||||
| chr13:111207515
|
C | T | 61 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(58): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(58): Show |
intron_variant | MODIFIER | c.337+2142C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111207515 | ||||||
| chr13:111207558
|
A | T | 2 | a0001c0002t0002g0174a0001c0002t0002g0211 | 2 | NA18964.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.337+2185A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111207558 | ||||||
| chr13:111207665
|
G | A | 5 | a0001c0001t0002g0099a0001c0003t0001g0142a0001c0003t0003g0021others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.338-2207G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111207665 | ||||||
| chr13:111207733
|
A | G | 207 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.338-2139A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111207733 | ||||||
| chr13:111207789
|
G | A | 3 | a0001c0001t0006g0032a0001c0001t0006g0083a0001c0001t0006g0234 | 3 | HG00558.hp2 NA18939.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.338-2083G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111207789 | ||||||
| chr13:111207920
|
A | C | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.338-1952A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111207920 | ||||||
| chr13:111207950
|
C | G | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.338-1922C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111207950 | ||||||
| chr13:111208039
|
A | G | 238 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.338-1833A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111208039 | ||||||
| chr13:111208042
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.338-1830C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111208042 | ||||||
| chr13:111208213
|
T | C | 2 | a0001c0001t0006g0032a0001c0001t0006g0083 | 2 | HG00558.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.338-1659T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111208213 | ||||||
| chr13:111208292
|
T | C | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.338-1580T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111208292 | ||||||
| chr13:111208365
|
C | G | 1 | a0001c0001t0004g0226 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.338-1507C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111208365 | ||||||
| chr13:111208369
|
G | T | 6 | a0001c0002t0002g0033a0001c0002t0002g0174a0001c0002t0002g0193others(3): Show | 6 | HG00558.hp1 NA18962.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.338-1503G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111208369 | ||||||
| chr13:111208606
|
A | C | 2 | a0001c0001t0005g0102a0001c0001t0005g0103 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.338-1266A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111208606 | ||||||
| chr13:111209044
|
C | T | 1 | a0001c0001t0003g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.338-828C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111209044 | ||||||
| chr13:111209054
|
A | G | 1 | a0006c0019t0002g0175 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.338-818A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111209054 | ||||||
| chr13:111209176
|
T | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.338-696T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111209176 | ||||||
| chr13:111209197
|
C | CT | 28 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(25): Show | 28 | HG00558.hp2 HG00642.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.338-667dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr13 | 111209197 | |||||
| chr13:111209260
|
G | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.338-612G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111209260 | ||||||
| chr13:111209280
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.338-592A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111209280 | ||||||
| chr13:111209360
|
G | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0066a0001c0001t0001g0074 | 3 | HG02647.hp2 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.338-512G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111209360 | ||||||
| chr13:111209556
|
G | A | 40 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.338-316G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111209556 | ||||||
| chr13:111209630
|
A | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.338-242A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 3/21 | chr13 | 111209630 | ||||||
| chr13:111210161
|
G | T | 1 | a0001c0015t0002g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.468+159G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111210161 | ||||||
| chr13:111210256
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.468+254C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111210256 | ||||||
| chr13:111210319
|
A | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(101): Show |
intron_variant | MODIFIER | c.468+317A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111210319 | ||||||
| chr13:111210526
|
C | T | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18941.hp2 NA18962.hp2 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+524C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111210526 | ||||||
| chr13:111210558
|
C | T | 3 | a0001c0001t0002g0091a0001c0001t0015g0271a0001c0001t0015g0273 | 3 | HG03453.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.468+556C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111210558 | ||||||
| chr13:111210727
|
G | A | 2 | a0001c0002t0002g0199a0001c0002t0002g0204 | 2 | NA18971.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.468+725G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111210727 | ||||||
| chr13:111210920
|
A | C | 41 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.468+918A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111210920 | ||||||
| chr13:111211105
|
T | C | 1 | a0001c0001t0005g0114 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.468+1103T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111211105 | ||||||
| chr13:111211120
|
C | T | 1 | a0001c0001t0007g0067 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.468+1118C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111211120 | ||||||
| chr13:111211373
|
C | T | 40 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.468+1371C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111211373 | ||||||
| chr13:111211399
|
A | AT | 8 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(5): Show | 8 | HG02559.hp1 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+1406dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr13 | 111211399 | |||||
| chr13:111211563
|
C | T | 1 | a0001c0001t0003g0266 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.468+1561C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111211563 | ||||||
| chr13:111212072
|
C | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.468+2070C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111212072 | ||||||
| chr13:111212129
|
A | C | 1 | a0001c0001t0003g0274 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.468+2127A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111212129 | ||||||
| chr13:111212329
|
C | T | 1 | a0001c0001t0004g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.468+2327C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111212329 | ||||||
| chr13:111212347
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.468+2345C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111212347 | ||||||
| chr13:111212372
|
C | A | 2 | a0001c0001t0003g0104a0001c0001t0003g0108 | 2 | HG00099.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.468+2370C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111212372 | ||||||
| chr13:111212391
|
G | A | 1 | a0001c0001t0003g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.468+2389G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111212391 | ||||||
| chr13:111212542
|
T | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.468+2540T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111212542 | ||||||
| chr13:111212716
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.468+2714C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111212716 | ||||||
| chr13:111212846
|
G | C | 24 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(21): Show | 24 | HG00099.hp2 HG00597.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.468+2844G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111212846 | ||||||
| chr13:111212921
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0007g0057 | 2 | HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.468+2919G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111212921 | ||||||
| chr13:111213242
|
G | A | 1 | a0001c0002t0002g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.468+3240G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111213242 | ||||||
| chr13:111213404
|
C | T | 5 | a0001c0001t0001g0040a0001c0001t0001g0231a0001c0001t0001g0232others(2): Show | 5 | NA18952.hp2 NA18957.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+3402C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111213404 | ||||||
| chr13:111213521
|
A | G | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.468+3519A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111213521 | ||||||
| chr13:111213703
|
C | T | 5 | a0001c0001t0002g0099a0001c0003t0001g0142a0001c0003t0003g0021others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+3701C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111213703 | ||||||
| chr13:111213739
|
C | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(4): Show | 7 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+3737C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111213739 | ||||||
| chr13:111213929
|
G | C | 3 | a0001c0002t0021g0255a0001c0002t0021g0256a0001c0002t0031g0130 | 3 | NA18957.hp1 NA18979.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.469-3750G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111213929 | ||||||
| chr13:111214173
|
G | A | 54 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(51): Show | 54 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.469-3506G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111214173 | ||||||
| chr13:111214177
|
C | T | 40 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.469-3502C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111214177 | ||||||
| chr13:111214478
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.469-3201C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111214478 | ||||||
| chr13:111214587
|
C | T | 40 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.469-3092C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111214587 | ||||||
| chr13:111214594
|
C | T | 2 | a0001c0001t0004g0133a0001c0001t0004g0134 | 2 | NA19066.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.469-3085C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111214594 | ||||||
| chr13:111214640
|
G | T | 1 | a0001c0001t0015g0273 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.469-3039G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111214640 | ||||||
| chr13:111214802
|
T | C | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.469-2877T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111214802 | ||||||
| chr13:111214860
|
AATAG | A | 76 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0001g0144others(73): Show | 76 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.469-2815_469-2812d others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr13 | 111214860 | |||||
| chr13:111214906
|
T | C | 1 | a0007c0010t0001g0095 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.469-2773T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111214906 | ||||||
| chr13:111215154
|
C | A | 207 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.469-2525C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111215154 | ||||||
| chr13:111215162
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0188 | 2 | HG01109.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.469-2517T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111215162 | ||||||
| chr13:111215231
|
G | A | 1 | a0001c0001t0006g0218 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.469-2448G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111215231 | ||||||
| chr13:111215371
|
CT | C | 158 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(155): Show | 158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.469-2299delT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr13 | 111215371 | |||||
| chr13:111215372
|
T | C | 9 | a0001c0001t0006g0083a0001c0001t0009g0171a0001c0001t0009g0202others(6): Show | 9 | NA18939.hp1 NA18941.hp2 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.469-2307T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111215372 | ||||||
| chr13:111215431
|
G | A | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.469-2248G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111215431 | ||||||
| chr13:111215454
|
C | G | 40 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.469-2225C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111215454 | ||||||
| chr13:111215553
|
C | T | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.469-2126C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111215553 | ||||||
| chr13:111215564
|
T | C | 235 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.469-2115T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111215564 | ||||||
| chr13:111215695
|
G | T | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.469-1984G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111215695 | ||||||
| chr13:111215815
|
C | T | 2 | a0001c0001t0003g0025a0001c0001t0004g0122 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.469-1864C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111215815 | ||||||
| chr13:111216195
|
C | A | 1 | a0001c0001t0003g0088 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.469-1484C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111216195 | ||||||
| chr13:111216404
|
C | G | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.469-1275C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111216404 | ||||||
| chr13:111216469
|
T | G | 56 | a0001c0001t0001g0019a0001c0001t0001g0129a0001c0001t0001g0137others(53): Show | 56 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.469-1210T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111216469 | ||||||
| chr13:111216688
|
G | A | 3 | a0001c0001t0003g0107a0001c0001t0003g0136a0001c0001t0003g0215 | 3 | HG01891.hp2 HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.469-991G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111216688 | ||||||
| chr13:111216701
|
G | A | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18941.hp2 NA18962.hp2 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.469-978G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111216701 | ||||||
| chr13:111216708
|
A | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(103): Show |
intron_variant | MODIFIER | c.469-971A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111216708 | ||||||
| chr13:111217085
|
A | T | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.469-594A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111217085 | ||||||
| chr13:111217323
|
AAGTGTTA others(7): Show |
A | 1 | a0001c0001t0006g0268 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.469-354_469-341del others(14): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr13 | 111217323 | |||||
| chr13:111217387
|
T | C | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.469-292T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111217387 | ||||||
| chr13:111217401
|
G | A | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.469-278G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111217401 | ||||||
| chr13:111217487
|
G | C | 1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.469-192G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111217487 | ||||||
| chr13:111217529
|
G | A | 1 | a0001c0001t0006g0218 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.469-150G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111217529 | ||||||
| chr13:111217629
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.469-50A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111217629 | ||||||
| chr13:111217673
|
T | G | 1 | a0001c0001t0008g0003 | 1 | HG03471.hp2 | splice_region_variant&intron_variant | LOW | c.469-6T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4/21 | chr13 | 111217673 | ||||||
| chr13:111218030
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.670+150C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111218030 | ||||||
| chr13:111218111
|
C | T | 2 | a0001c0001t0001g0125a0001c0013t0001g0100 | 2 | HG00642.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.670+231C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111218111 | ||||||
| chr13:111218168
|
CT | C | 6 | a0001c0001t0006g0032a0001c0001t0008g0017a0001c0001t0009g0202others(3): Show | 6 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+303delT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111218168 | |||||
| chr13:111218183
|
T | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.670+303T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111218183 | ||||||
| chr13:111218244
|
A | G | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+364A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111218244 | ||||||
| chr13:111218293
|
C | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0096 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.670+413C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111218293 | ||||||
| chr13:111218375
|
G | A | 32 | a0001c0001t0001g0068a0001c0001t0002g0078a0001c0001t0002g0164others(29): Show | 32 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.670+495G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111218375 | ||||||
| chr13:111218578
|
A | G | 107 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.670+698A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111218578 | ||||||
| chr13:111218696
|
C | T | 2 | a0001c0002t0002g0257a0001c0002t0006g0236 | 2 | NA18966.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.670+816C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111218696 | ||||||
| chr13:111218868
|
G | T | 1 | a0001c0001t0007g0028 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.670+988G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111218868 | ||||||
| chr13:111219071
|
T | G | 6 | a0001c0002t0002g0033a0001c0002t0002g0174a0001c0002t0002g0193others(3): Show | 6 | HG00558.hp1 NA18962.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.670+1191T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111219071 | ||||||
| chr13:111219233
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.670+1353G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111219233 | ||||||
| chr13:111219376
|
G | A | 4 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017others(1): Show | 4 | HG01109.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+1496G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111219376 | ||||||
| chr13:111219410
|
C | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.670+1530C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111219410 | ||||||
| chr13:111219423
|
G | A | 40 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.670+1543G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111219423 | ||||||
| chr13:111219590
|
C | T | 1 | a0001c0007t0004g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.670+1710C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111219590 | ||||||
| chr13:111219645
|
G | GT | 5 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0014g0186others(2): Show | 5 | HG01928.hp1 HG02135.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.670+1776dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111219645 | |||||
| chr13:111219645
|
GT | G | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.670+1776delT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111219645 | |||||
| chr13:111219733
|
G | A | 8 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(5): Show | 8 | HG02559.hp1 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.670+1853G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111219733 | ||||||
| chr13:111219926
|
A | C | 19 | a0001c0001t0001g0040a0001c0001t0001g0047a0001c0001t0001g0049others(16): Show | 19 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.670+2046A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111219926 | ||||||
| chr13:111220039
|
G | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.670+2159G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111220039 | ||||||
| chr13:111220044
|
GGCCT | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(2): Show | 5 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+2167_670+2170d others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111220044 | |||||
| chr13:111220174
|
C | T | 17 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0097others(14): Show | 17 | HG00140.hp2 HG00642.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.670+2294C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111220174 | ||||||
| chr13:111220192
|
G | A | 2 | a0001c0001t0003g0119a0001c0001t0033g0101 | 2 | HG00738.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.670+2312G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111220192 | ||||||
| chr13:111220325
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0015g0272 | 3 | HG02145.hp2 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.670+2445G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111220325 | ||||||
| chr13:111220654
|
C | T | 10 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0051others(7): Show | 10 | HG00099.hp1 HG00280.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.670+2774C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111220654 | ||||||
| chr13:111220811
|
G | A | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.670+2931G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111220811 | ||||||
| chr13:111220891
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.670+3011A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111220891 | ||||||
| chr13:111220926
|
G | A | 1 | a0001c0001t0029g0201 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.670+3046G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111220926 | ||||||
| chr13:111220944
|
TGTTA | T | 105 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(102): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.670+3069_670+3072d others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111220944 | |||||
| chr13:111220949
|
G | T | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.670+3069G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111220949 | ||||||
| chr13:111221027
|
T | A | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+3147T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221027 | ||||||
| chr13:111221064
|
T | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.670+3184T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221064 | ||||||
| chr13:111221089
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.670+3209A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221089 | ||||||
| chr13:111221092
|
G | C | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18941.hp2 NA18962.hp2 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.670+3212G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221092 | ||||||
| chr13:111221138
|
CATATATA others(21): Show |
C | 1 | a0001c0005t0020g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.670+3263_670+3290d others(30): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221138 | |||||
| chr13:111221138
|
CATATATA others(49): Show |
C | 1 | a0001c0001t0004g0241 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.670+3263_670+3318d others(58): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221138 | |||||
| chr13:111221138
|
CATATATA others(105): Show |
C | 1 | a0001c0001t0001g0039 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.670+3263_670+3374d others(2): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221138 | |||||
| chr13:111221139
|
ATATATAT others(99): Show |
A | 8 | a0001c0001t0001g0084a0001c0001t0007g0094a0001c0001t0008g0003others(5): Show | 8 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.670+3269_670+3374d others(2): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221139 | |||||
| chr13:111221139
|
ATATATAT others(127): Show |
A | 1 | a0001c0001t0023g0037 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.670+3269_670+3402d others(2): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221139 | |||||
| chr13:111221143
|
A | ATATATAG others(49): Show |
1 | a0001c0001t0007g0008 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.670+3382_670+3437d others(58): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221143 | |||||
| chr13:111221143
|
A | C | 79 | a0001c0001t0001g0019a0001c0001t0001g0129a0001c0001t0001g0137others(76): Show | 79 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.670+3263A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221143 | ||||||
| chr13:111221143
|
ATATATAG others(21): Show |
A | 5 | a0001c0001t0002g0078a0001c0001t0004g0065a0001c0001t0004g0086others(2): Show | 5 | HG01167.hp2 HG02647.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+3410_670+3437d others(30): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221143 | |||||
| chr13:111221143
|
ATATATAG others(49): Show |
A | 8 | a0001c0001t0004g0122a0001c0001t0004g0133a0001c0001t0004g0134others(5): Show | 8 | HG00280.hp2 HG02135.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.670+3382_670+3437d others(58): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221143 | |||||
| chr13:111221143
|
ATATATAG others(77): Show |
A | 6 | a0001c0001t0007g0004a0001c0001t0007g0009a0001c0001t0007g0028others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.670+3354_670+3437d others(86): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221143 | |||||
| chr13:111221143
|
ATATATAG others(105): Show |
A | 4 | a0001c0001t0001g0096a0001c0001t0001g0220a0001c0001t0012g0001others(1): Show | 4 | HG01891.hp1 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+3326_670+3437d others(2): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221143 | |||||
| chr13:111221167
|
A | G | 102 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(99): Show | 102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.670+3287A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221167 | ||||||
| chr13:111221180
|
TATATATG others(103): Show |
T | 2 | a0001c0001t0015g0271a0001c0001t0015g0273 | 2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.670+3307_670+3416d others(2): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221180 | |||||
| chr13:111221182
|
T | TATATGTC others(17): Show |
1 | a0001c0002t0002g0060 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.670+3307_670+3330d others(26): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221182 | |||||
| chr13:111221187
|
G | A | 102 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(99): Show | 102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.670+3307G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221187 | ||||||
| chr13:111221196
|
T | G | 1 | a0001c0001t0003g0119 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.670+3316T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221196 | ||||||
| chr13:111221197
|
A | C | 39 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.670+3317A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221197 | ||||||
| chr13:111221199
|
C | A | 40 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.670+3319C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221199 | ||||||
| chr13:111221201
|
ATATAGAT others(75): Show |
A | 6 | a0001c0001t0011g0006a0001c0001t0011g0007a0001c0001t0011g0055others(3): Show | 6 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+3326_670+3407d others(84): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221201 | |||||
| chr13:111221203
|
ATAGATAT others(63): Show |
A | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.670+3326_670+3395d others(72): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221203 | |||||
| chr13:111221205
|
AGATATAT others(117): Show |
A | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.670+3326_670+3449d others(2): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221205 | ||||||
| chr13:111221205
|
AGATATAT others(129): Show |
A | 60 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.670+3326_670+3461d others(2): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221205 | ||||||
| chr13:111221208
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0003g0119 | 2 | HG00738.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.670+3328T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221208 | ||||||
| chr13:111221213
|
ATGTCTAT others(131): Show |
A | 8 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0107others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.670+3335_670+3472d others(2): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221213 | |||||
| chr13:111221215
|
G | A | 32 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(29): Show | 32 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.670+3335G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221215 | ||||||
| chr13:111221216
|
T | G | 31 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.670+3336T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221216 | ||||||
| chr13:111221217
|
C | A | 31 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.670+3337C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221217 | ||||||
| chr13:111221218
|
T | C | 31 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.670+3338T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221218 | ||||||
| chr13:111221218
|
TATATATA others(209): Show |
T | 1 | a0001c0001t0003g0119 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.670+3347_670+3562d others(2): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221218 | |||||
| chr13:111221227
|
C | CTA | 3 | a0001c0001t0001g0019a0001c0001t0003g0085a0001c0001t0017g0269 | 3 | HG02451.hp2 HG03704.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.670+3352_670+3353d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221227 | |||||
| chr13:111221228
|
TATATAGA others(199): Show |
T | 31 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.670+3354_670+3559d others(2): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221228 | |||||
| chr13:111221229
|
ATATAGAT others(47): Show |
A | 1 | a0001c0001t0011g0070 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.670+3354_670+3407d others(56): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221229 | |||||
| chr13:111221237
|
ATATATGT others(1): Show |
A | 4 | a0001c0001t0004g0222a0001c0001t0004g0223a0001c0001t0004g0224others(1): Show | 4 | HG01261.hp2 HG02109.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+3363_670+3370d others(10): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221237 | |||||
| chr13:111221237
|
ATATATGT others(29): Show |
A | 1 | a0001c0001t0004g0226 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.670+3363_670+3398d others(38): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221237 | |||||
| chr13:111221253
|
ATCTATAT others(91): Show |
A | 1 | a0001c0001t0003g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.670+3382_670+3479d others(100): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221253 | |||||
| chr13:111221257
|
A | G | 1 | a0001c0001t0007g0132 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.670+3377A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221257 | ||||||
| chr13:111221257
|
ATATAGAT others(19): Show |
A | 1 | a0001c0001t0002g0164 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.670+3382_670+3407d others(28): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221257 | |||||
| chr13:111221271
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0017g0269 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.670+3391G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221271 | ||||||
| chr13:111221278
|
T | G | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.670+3398T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221278 | ||||||
| chr13:111221279
|
A | G | 1 | a0001c0001t0001g0220 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.670+3399A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221279 | ||||||
| chr13:111221281
|
ATCTATAT others(63): Show |
A | 2 | a0001c0001t0004g0238a0001c0001t0004g0247 | 2 | HG00323.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.670+3410_670+3479d others(72): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221281 | |||||
| chr13:111221282
|
T | G | 1 | a0001c0015t0002g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.670+3402T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221282 | ||||||
| chr13:111221283
|
C | A | 3 | a0001c0001t0016g0143a0001c0001t0019g0071a0001c0015t0002g0023 | 3 | HG02922.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.670+3403C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221283 | ||||||
| chr13:111221283
|
C | CTA | 5 | a0001c0001t0002g0251a0001c0001t0004g0222a0001c0001t0004g0223others(2): Show | 5 | HG01261.hp2 HG02109.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+3408_670+3409d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221283 | |||||
| chr13:111221283
|
C | CTATATAG others(23): Show |
1 | a0001c0001t0004g0261 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.670+3440_670+3469d others(32): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221283 | |||||
| chr13:111221288
|
T | G | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.670+3408T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221288 | ||||||
| chr13:111221290
|
G | C | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.670+3410G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221290 | ||||||
| chr13:111221290
|
G | T | 9 | a0001c0001t0001g0084a0001c0001t0007g0094a0001c0001t0008g0003others(6): Show | 9 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.670+3410G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221290 | ||||||
| chr13:111221291
|
A | G | 1 | a0001c0015t0002g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.670+3411A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221291 | ||||||
| chr13:111221292
|
T | G | 8 | a0001c0001t0001g0084a0001c0001t0007g0094a0001c0001t0008g0003others(5): Show | 8 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.670+3412T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221292 | ||||||
| chr13:111221293
|
A | C | 1 | a0001c0015t0002g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.670+3413A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221293 | ||||||
| chr13:111221293
|
ATATATGT others(51): Show |
A | 2 | a0001c0001t0001g0019a0001c0001t0017g0269 | 2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.670+3415_670+3472d others(60): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221293 | |||||
| chr13:111221297
|
ATGTC | A | 8 | a0001c0001t0001g0084a0001c0001t0007g0094a0001c0001t0008g0003others(5): Show | 8 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.670+3419_670+3422d others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221297 | |||||
| chr13:111221299
|
G | A | 4 | a0001c0001t0001g0220a0001c0001t0015g0271a0001c0001t0015g0273others(1): Show | 4 | HG03130.hp1 HG03453.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+3419G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221299 | ||||||
| chr13:111221299
|
G | C | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.670+3419G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221299 | ||||||
| chr13:111221301
|
C | A | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.670+3421C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221301 | ||||||
| chr13:111221306
|
T | G | 8 | a0001c0001t0001g0084a0001c0001t0007g0094a0001c0001t0008g0003others(5): Show | 8 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.670+3426T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221306 | ||||||
| chr13:111221307
|
A | G | 1 | a0001c0002t0010g0159 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.670+3427A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221307 | ||||||
| chr13:111221308
|
T | C | 8 | a0001c0001t0001g0084a0001c0001t0007g0094a0001c0001t0008g0003others(5): Show | 8 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.670+3428T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221308 | ||||||
| chr13:111221310
|
T | G | 1 | a0001c0015t0002g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.670+3430T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221310 | ||||||
| chr13:111221311
|
C | A | 9 | a0001c0001t0001g0084a0001c0001t0007g0094a0001c0001t0008g0003others(6): Show | 9 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.670+3431C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221311 | ||||||
| chr13:111221311
|
CTA | C | 102 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0001g0144others(99): Show | 102 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.670+3438_670+3439d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221311 | |||||
| chr13:111221312
|
TATATATA others(1): Show |
T | 7 | a0001c0001t0011g0006a0001c0001t0011g0007a0001c0001t0011g0055others(4): Show | 7 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+3440_670+3447d others(10): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221312 | |||||
| chr13:111221314
|
TATATAG | T | 5 | a0001c0001t0002g0164a0001c0001t0004g0222a0001c0001t0004g0223others(2): Show | 5 | HG01261.hp2 HG02109.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+3440_670+3445d others(8): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221314 | |||||
| chr13:111221317
|
A | C | 8 | a0001c0001t0001g0084a0001c0001t0007g0094a0001c0001t0008g0003others(5): Show | 8 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.670+3437A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221317 | ||||||
| chr13:111221320
|
G | T | 8 | a0001c0001t0001g0084a0001c0001t0007g0094a0001c0001t0008g0003others(5): Show | 8 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.670+3440G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221320 | ||||||
| chr13:111221322
|
T | C | 1 | a0001c0015t0002g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.670+3442T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221322 | ||||||
| chr13:111221323
|
A | C | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.670+3443A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221323 | ||||||
| chr13:111221328
|
T | C | 8 | a0001c0001t0001g0084a0001c0001t0007g0094a0001c0001t0008g0003others(5): Show | 8 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.670+3448T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221328 | ||||||
| chr13:111221329
|
G | A | 18 | a0001c0001t0001g0220a0001c0001t0003g0025a0001c0001t0004g0122others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.670+3449G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221329 | ||||||
| chr13:111221329
|
G | C | 13 | a0001c0001t0001g0084a0001c0001t0002g0164a0001c0001t0004g0222others(10): Show | 13 | HG01261.hp2 HG02109.hp2 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.670+3449G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221329 | ||||||
| chr13:111221330
|
T | G | 10 | a0001c0001t0001g0220a0001c0001t0003g0025a0001c0001t0004g0122others(7): Show | 10 | HG01243.hp1 HG02559.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.670+3450T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221330 | ||||||
| chr13:111221331
|
C | A | 26 | a0001c0001t0001g0084a0001c0001t0001g0220a0001c0001t0002g0164others(23): Show | 26 | HG01243.hp1 HG01261.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.670+3451C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221331 | ||||||
| chr13:111221332
|
T | C | 10 | a0001c0001t0001g0220a0001c0001t0003g0025a0001c0001t0004g0122others(7): Show | 10 | HG01243.hp1 HG02559.hp1 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.670+3452T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221332 | ||||||
| chr13:111221332
|
T | G | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.670+3452T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221332 | ||||||
| chr13:111221337
|
A | C | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.670+3457A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221337 | ||||||
| chr13:111221337
|
A | G | 3 | a0001c0002t0010g0081a0001c0002t0010g0159a0001c0002t0010g0197 | 3 | NA18968.hp2 NA18999.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.670+3457A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221337 | ||||||
| chr13:111221341
|
C | A | 3 | a0001c0001t0005g0062a0001c0001t0016g0143a0001c0001t0019g0071 | 3 | HG02257.hp2 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.670+3461C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221341 | ||||||
| chr13:111221342
|
T | G | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.670+3462T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221342 | ||||||
| chr13:111221342
|
T | TATATAG | 76 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0002g0011others(73): Show | 76 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.670+3467_670+3468i others(8): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221342 | |||||
| chr13:111221344
|
T | C | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.670+3464T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221344 | ||||||
| chr13:111221344
|
T | G | 60 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(57): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.670+3464T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221344 | ||||||
| chr13:111221344
|
T | TATAGATA others(207): Show |
1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.670+3467_670+3468i others(216): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221344 | |||||
| chr13:111221344
|
T | TATAGATA others(179): Show |
2 | a0001c0001t0001g0144a0001c0001t0008g0017 | 2 | HG01109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.670+3467_670+3468i others(188): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221344 | |||||
| chr13:111221345
|
A | ATAGATAT others(292): Show |
1 | a0001c0001t0005g0139 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.670+3467_670+3468i others(301): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221345 | |||||
| chr13:111221346
|
T | TAGAGATA others(91): Show |
1 | a0001c0001t0006g0032 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.670+3467_670+3468i others(100): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221346 | |||||
| chr13:111221346
|
T | TAGATATA others(175): Show |
1 | a0001c0001t0006g0234 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.670+3467_670+3468i others(184): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221346 | |||||
| chr13:111221346
|
T | TAGATATA others(147): Show |
1 | a0001c0001t0006g0185 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.670+3467_670+3468i others(156): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221346 | |||||
| chr13:111221346
|
T | TAGATATA others(119): Show |
5 | a0001c0001t0006g0090a0001c0001t0006g0218a0001c0001t0006g0263others(2): Show | 5 | HG00642.hp1 HG01993.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.670+3467_670+3468i others(128): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221346 | |||||
| chr13:111221346
|
T | TAGATATA others(91): Show |
5 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0014g0153others(2): Show | 5 | HG01928.hp1 HG01943.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.670+3467_670+3468i others(100): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221346 | |||||
| chr13:111221347
|
A | AGATATAT others(348): Show |
1 | a0001c0001t0005g0230 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.670+3467_670+3468i others(357): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221347 | ||||||
| chr13:111221347
|
ATATGTC | A | 6 | a0001c0001t0017g0270a0001c0002t0002g0147a0001c0002t0002g0150others(3): Show | 6 | HG01175.hp1 HG02132.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.670+3471_670+3476d others(8): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221347 | |||||
| chr13:111221348
|
T | G | 9 | a0001c0001t0011g0006a0001c0001t0011g0007a0001c0001t0011g0055others(6): Show | 9 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.670+3468T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221348 | ||||||
| chr13:111221350
|
T | G | 1 | a0001c0001t0004g0242 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.670+3470T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221350 | ||||||
| chr13:111221351
|
G | A | 144 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(141): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.670+3471G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221351 | ||||||
| chr13:111221352
|
T | C | 1 | a0001c0001t0023g0037 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.670+3472T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221352 | ||||||
| chr13:111221353
|
C | A | 71 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(68): Show | 71 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.670+3473C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221353 | ||||||
| chr13:111221353
|
C | G | 1 | a0001c0002t0002g0060 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.670+3473C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221353 | ||||||
| chr13:111221353
|
CTA | C | 4 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0003g0025others(1): Show | 4 | HG01891.hp1 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+3483_670+3484d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221353 | |||||
| chr13:111221354
|
T | G | 74 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(71): Show | 74 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.670+3474T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221354 | ||||||
| chr13:111221355
|
A | C | 1 | a0001c0002t0002g0060 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.670+3475A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221355 | ||||||
| chr13:111221356
|
T | C | 67 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(64): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.670+3476T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221356 | ||||||
| chr13:111221356
|
T | TATATATC others(7): Show |
51 | a0001c0001t0001g0129a0001c0001t0003g0024a0001c0001t0005g0126others(48): Show | 51 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.670+3482_670+3483i others(16): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221356 | |||||
| chr13:111221356
|
T | TATATATC others(885): Show |
1 | a0001c0001t0009g0258 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.670+3482_670+3483i others(894): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221356 | |||||
| chr13:111221356
|
T | TATATATC others(885): Show |
1 | a0001c0001t0009g0260 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.670+3482_670+3483i others(894): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221356 | |||||
| chr13:111221356
|
T | TATATATC others(885): Show |
1 | a0001c0001t0009g0259 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.670+3482_670+3483i others(894): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221356 | |||||
| chr13:111221356
|
T | TATATATC others(961): Show |
1 | a0001c0001t0009g0214 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.670+3482_670+3483i others(970): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221356 | |||||
| chr13:111221356
|
T | TATATATC others(831): Show |
1 | a0001c0001t0009g0171 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.670+3482_670+3483i others(840): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221356 | |||||
| chr13:111221356
|
T | TATATATC others(389): Show |
1 | a0001c0001t0029g0201 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.670+3482_670+3483i others(398): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221356 | |||||
| chr13:111221356
|
T | TATATCTA others(5): Show |
1 | a0001c0001t0001g0137 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.670+3480_670+3481i others(14): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221356 | |||||
| chr13:111221358
|
T | TATATCTA others(5): Show |
1 | a0001c0001t0006g0083 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.670+3482_670+3483i others(14): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221358 | |||||
| chr13:111221360
|
T | G | 16 | a0001c0001t0001g0144a0001c0001t0006g0032a0001c0001t0006g0041others(13): Show | 16 | HG00558.hp2 HG00642.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.670+3480T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221360 | ||||||
| chr13:111221360
|
T | TATCTATA others(203): Show |
1 | a0003c0011t0005g0191 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.670+3482_670+3483i others(212): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221360 | |||||
| chr13:111221361
|
A | ATCTATAT others(123): Show |
1 | a0001c0006t0012g0124 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.670+3482_670+3483i others(132): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221361 | |||||
| chr13:111221362
|
T | TCTATATA others(691): Show |
1 | a0001c0001t0009g0250 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.670+3482_670+3483i others(700): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221362 | ||||||
| chr13:111221363
|
A | C | 15 | a0001c0001t0002g0011a0001c0001t0002g0099a0001c0001t0003g0128others(12): Show | 15 | HG00741.hp1 HG01081.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.670+3483A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221363 | ||||||
| chr13:111221363
|
A | G | 7 | a0001c0001t0007g0008a0001c0001t0017g0270a0001c0002t0002g0147others(4): Show | 7 | HG01175.hp1 HG02132.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.670+3483A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221363 | ||||||
| chr13:111221364
|
T | C | 1 | a0001c0001t0009g0250 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.670+3484T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221364 | ||||||
| chr13:111221364
|
T | G | 21 | a0001c0001t0001g0019a0001c0001t0001g0084a0001c0001t0001g0220others(18): Show | 21 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.670+3484T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221364 | ||||||
| chr13:111221365
|
C | A | 39 | a0001c0001t0001g0019a0001c0001t0001g0084a0001c0001t0001g0220others(36): Show | 39 | HG00741.hp1 HG01081.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.670+3485C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221365 | ||||||
| chr13:111221365
|
C | G | 55 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(52): Show | 55 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.670+3485C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221365 | ||||||
| chr13:111221367
|
A | C | 55 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(52): Show | 55 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.670+3487A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221367 | ||||||
| chr13:111221367
|
A | G | 9 | a0001c0001t0001g0084a0001c0001t0002g0164a0001c0001t0007g0094others(6): Show | 9 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.670+3487A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221367 | ||||||
| chr13:111221368
|
T | TAGATATA others(299): Show |
1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.670+3489_670+3490i others(308): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221368 | |||||
| chr13:111221368
|
T | TAGATATA others(177): Show |
2 | a0001c0001t0002g0011a0001c0001t0016g0012 | 2 | HG02895.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.670+3489_670+3490i others(186): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221368 | |||||
| chr13:111221368
|
T | TAGATATA others(65): Show |
1 | a0001c0002t0002g0082 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.670+3489_670+3490i others(74): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221368 | |||||
| chr13:111221368
|
T | TAGATATA others(233): Show |
1 | a0001c0006t0012g0121 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.670+3489_670+3490i others(242): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221368 | |||||
| chr13:111221369
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0007g0010a0001c0001t0023g0036 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.670+3530_670+3553d others(26): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221369 | |||||
| chr13:111221369
|
A | C | 18 | a0001c0001t0001g0019a0001c0001t0001g0084a0001c0001t0002g0164others(15): Show | 18 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.670+3489A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221369 | ||||||
| chr13:111221370
|
T | G | 10 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(7): Show | 10 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.670+3490T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221370 | ||||||
| chr13:111221372
|
T | C | 1 | a0003c0011t0005g0191 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.670+3492T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221372 | ||||||
| chr13:111221372
|
T | G | 6 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0002t0002g0060others(3): Show | 6 | HG01081.hp2 HG01891.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+3492T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221372 | ||||||
| chr13:111221373
|
A | ATATATGT others(314): Show |
2 | a0001c0001t0005g0102a0001c0001t0005g0103 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.670+3496_670+3497i others(323): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221373 | |||||
| chr13:111221373
|
A | ATATATGT others(344): Show |
1 | a0001c0001t0003g0128 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.670+3496_670+3497i others(353): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221373 | |||||
| chr13:111221373
|
A | ATATATGT others(316): Show |
1 | a0001c0001t0005g0063 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.670+3496_670+3497i others(325): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221373 | |||||
| chr13:111221373
|
A | ATATATGT others(288): Show |
1 | a0001c0001t0005g0115 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.670+3496_670+3497i others(297): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221373 | |||||
| chr13:111221373
|
A | ATATATGT others(232): Show |
2 | a0001c0001t0005g0140a0001c0001t0005g0141 | 2 | HG01257.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.670+3496_670+3497i others(241): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221373 | |||||
| chr13:111221375
|
A | ATATGTCT others(312): Show |
1 | a0001c0001t0005g0114 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.670+3496_670+3497i others(321): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221375 | |||||
| chr13:111221375
|
A | ATATGTCT others(286): Show |
1 | a0001c0001t0005g0212 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.670+3496_670+3497i others(295): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221375 | |||||
| chr13:111221375
|
A | C | 5 | a0001c0001t0017g0270a0001c0002t0002g0147a0001c0002t0002g0150others(2): Show | 5 | HG01175.hp1 HG02132.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.670+3495A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221375 | ||||||
| chr13:111221377
|
C | A | 19 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(16): Show | 19 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.670+3497C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221377 | ||||||
| chr13:111221377
|
CTA | C | 13 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(10): Show | 13 | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.670+3506_670+3507d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221377 | |||||
| chr13:111221381
|
A | AGACATAT others(5): Show |
1 | a0001c0002t0002g0157 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.670+3501_670+3502i others(14): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221381 | ||||||
| chr13:111221381
|
A | C | 1 | a0001c0001t0009g0250 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.670+3501A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221381 | ||||||
| chr13:111221382
|
T | G | 7 | a0001c0001t0017g0270a0001c0002t0002g0060a0001c0002t0002g0147others(4): Show | 7 | HG01175.hp1 HG02132.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.670+3502T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221382 | ||||||
| chr13:111221382
|
T | TAG | 51 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(48): Show | 51 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.670+3503_670+3504i others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221382 | |||||
| chr13:111221384
|
T | C | 1 | a0001c0002t0002g0060 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.670+3504T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221384 | ||||||
| chr13:111221384
|
T | G | 4 | a0001c0001t0002g0011a0001c0001t0016g0012a0001c0002t0002g0082others(1): Show | 4 | HG00741.hp1 HG02895.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+3504T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221384 | ||||||
| chr13:111221386
|
TAG | T | 6 | a0001c0001t0009g0171a0001c0001t0009g0214a0001c0001t0009g0258others(3): Show | 6 | NA18941.hp2 NA19000.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.670+3508_670+3509d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221386 | |||||
| chr13:111221388
|
G | T | 76 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0002g0011others(73): Show | 76 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.670+3508G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221388 | ||||||
| chr13:111221389
|
A | C | 5 | a0001c0001t0002g0011a0001c0001t0002g0099a0001c0001t0016g0012others(2): Show | 5 | HG00741.hp1 HG02895.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+3509A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221389 | ||||||
| chr13:111221389
|
A | G | 6 | a0001c0001t0009g0171a0001c0001t0009g0214a0001c0001t0009g0258others(3): Show | 6 | NA18941.hp2 NA19000.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.670+3509A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221389 | ||||||
| chr13:111221389
|
ATG | A | 11 | a0001c0001t0001g0016a0001c0001t0001g0066a0001c0001t0001g0074others(8): Show | 11 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.670+3511_670+3512d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221389 | |||||
| chr13:111221390
|
TGTCTATA others(37): Show |
T | 3 | a0001c0001t0001g0123a0001c0001t0001g0219a0001c0001t0001g0220 | 3 | HG00099.hp1 NA19057.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.670+3511_670+3554d others(46): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221390 | ||||||
| chr13:111221391
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(90): Show | 93 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.670+3511G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221391 | ||||||
| chr13:111221391
|
G | C | 6 | a0001c0001t0009g0171a0001c0001t0009g0214a0001c0001t0009g0258others(3): Show | 6 | NA18941.hp2 NA19000.hp1 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.670+3511G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221391 | ||||||
| chr13:111221393
|
C | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(85): Show | 88 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.670+3513C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221393 | ||||||
| chr13:111221393
|
C | CTA | 30 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(27): Show | 30 | HG00558.hp1 HG00597.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.670+3519_670+3520d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221393 | |||||
| chr13:111221393
|
C | CTATA | 4 | a0001c0001t0001g0144a0001c0001t0008g0017a0001c0002t0002g0157others(1): Show | 4 | HG01109.hp1 HG01192.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+3517_670+3520d others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221393 | |||||
| chr13:111221396
|
T | G | 13 | a0001c0001t0002g0029a0001c0001t0002g0091a0001c0001t0002g0156others(10): Show | 13 | HG01081.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.670+3516T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221396 | ||||||
| chr13:111221398
|
T | C | 13 | a0001c0001t0001g0229a0001c0001t0002g0029a0001c0001t0002g0091others(10): Show | 13 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.670+3518T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221398 | ||||||
| chr13:111221399
|
A | ATATCTAT others(209): Show |
1 | a0001c0003t0019g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.670+3520_670+3521i others(218): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221399 | |||||
| chr13:111221399
|
A | ATATCTAT others(237): Show |
1 | a0001c0003t0003g0021 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.670+3520_670+3521i others(246): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221399 | |||||
| chr13:111221399
|
A | ATATCTAT others(265): Show |
1 | a0001c0003t0003g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.670+3520_670+3521i others(274): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221399 | |||||
| chr13:111221399
|
A | ATATCTAT others(321): Show |
1 | a0001c0003t0001g0142 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.670+3520_670+3521i others(330): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221399 | |||||
| chr13:111221401
|
C | A | 37 | a0001c0001t0006g0083a0001c0002t0001g0170a0001c0002t0001g0182others(34): Show | 37 | HG00323.hp2 HG01257.hp1 HG01361.hp2 others(34): Show |
intron_variant | MODIFIER | c.670+3521C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221401 | ||||||
| chr13:111221401
|
C | CTATATAT others(5): Show |
1 | a0001c0001t0005g0139 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.670+3523_670+3534d others(14): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221401 | |||||
| chr13:111221401
|
CTA | C | 13 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(10): Show | 13 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.670+3530_670+3531d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221401 | |||||
| chr13:111221402
|
T | G | 1 | a0001c0002t0002g0060 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.670+3522T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221402 | ||||||
| chr13:111221403
|
A | C | 36 | a0001c0001t0006g0083a0001c0002t0001g0170a0001c0002t0001g0182others(33): Show | 36 | HG00323.hp2 HG01257.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.670+3523A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221403 | ||||||
| chr13:111221406
|
T | TAG | 20 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(17): Show | 20 | HG00558.hp1 HG00597.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.670+3527_670+3528i others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221406 | |||||
| chr13:111221410
|
T | G | 1 | a0001c0001t0002g0164 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.670+3530T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221410 | ||||||
| chr13:111221412
|
G | T | 21 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(18): Show | 21 | HG00558.hp1 HG00597.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.670+3532G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221412 | ||||||
| chr13:111221412
|
GATGTCTA others(27): Show |
G | 8 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0107others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.670+3535_670+3568d others(36): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221412 | |||||
| chr13:111221414
|
TGTCTATA others(13): Show |
T | 39 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0047others(36): Show | 39 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.670+3535_670+3554d others(22): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221414 | ||||||
| chr13:111221415
|
G | A | 108 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(105): Show | 108 | HG00140.hp2 HG00323.hp2 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.670+3535G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221415 | ||||||
| chr13:111221416
|
T | G | 1 | a0001c0001t0003g0184 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.670+3536T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221416 | ||||||
| chr13:111221417
|
C | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(60): Show | 63 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.670+3537C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221417 | ||||||
| chr13:111221417
|
C | CTA | 7 | a0001c0002t0002g0031a0001c0002t0002g0147a0001c0002t0002g0165others(4): Show | 7 | HG00597.hp2 HG01175.hp1 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+3543_670+3544d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221417 | |||||
| chr13:111221418
|
T | C | 1 | a0001c0001t0003g0184 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.670+3538T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221418 | ||||||
| chr13:111221420
|
T | G | 25 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(22): Show | 25 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.670+3540T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221420 | ||||||
| chr13:111221421
|
A | C | 1 | a0001c0001t0003g0184 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.670+3541A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221421 | ||||||
| chr13:111221422
|
T | C | 25 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(22): Show | 25 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.670+3542T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221422 | ||||||
| chr13:111221422
|
T | G | 35 | a0001c0002t0001g0170a0001c0002t0001g0182a0001c0002t0002g0046others(32): Show | 35 | HG00323.hp2 HG01257.hp1 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.670+3542T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221422 | ||||||
| chr13:111221423
|
A | ATATCTAT others(97): Show |
1 | a0001c0001t0009g0202 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.670+3544_670+3545i others(106): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221423 | |||||
| chr13:111221424
|
T | C | 35 | a0001c0002t0001g0170a0001c0002t0001g0182a0001c0002t0002g0046others(32): Show | 35 | HG00323.hp2 HG01257.hp1 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.670+3544T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221424 | ||||||
| chr13:111221425
|
C | A | 65 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0002g0011others(62): Show | 65 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.670+3545C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221425 | ||||||
| chr13:111221425
|
C | CTA | 28 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0084others(25): Show | 28 | HG01109.hp1 HG01192.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.670+3552_670+3553d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221425 | |||||
| chr13:111221427
|
A | C | 12 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(9): Show | 12 | HG00558.hp1 HG01081.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.670+3547A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221427 | ||||||
| chr13:111221428
|
T | G | 11 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(8): Show | 11 | HG00558.hp2 HG01928.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.670+3548T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221428 | ||||||
| chr13:111221429
|
A | C | 5 | a0001c0001t0002g0099a0001c0003t0001g0142a0001c0003t0003g0021others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.670+3549A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221429 | ||||||
| chr13:111221432
|
T | G | 1 | a0001c0001t0003g0184 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.670+3552T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221432 | ||||||
| chr13:111221432
|
T | TATAG | 11 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(8): Show | 11 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.670+3553_670+3554i others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221432 | |||||
| chr13:111221432
|
TAG | T | 3 | a0001c0001t0002g0099a0001c0003t0003g0021a0001c0003t0019g0022 | 3 | HG02451.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.670+3554_670+3555d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221432 | |||||
| chr13:111221433
|
A | ATAGATAT others(127): Show |
1 | a0001c0001t0006g0234 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.670+3553_670+3554i others(136): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221433 | ||||||
| chr13:111221433
|
A | ATATATAG others(103): Show |
3 | a0001c0001t0006g0032a0001c0001t0006g0090a0001c0001t0006g0218 | 3 | HG00558.hp2 HG02622.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.670+3553_670+3554i others(112): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221433 | ||||||
| chr13:111221433
|
A | C | 36 | a0001c0001t0006g0083a0001c0002t0001g0170a0001c0002t0001g0182others(33): Show | 36 | HG00323.hp2 HG01257.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.670+3553A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221433 | ||||||
| chr13:111221434
|
G | GATATCTA others(121): Show |
1 | a0001c0001t0013g0162 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.670+3558_670+3559i others(130): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221434 | |||||
| chr13:111221434
|
G | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(92): Show | 95 | HG00140.hp2 HG00323.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.670+3554G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221434 | ||||||
| chr13:111221436
|
T | C | 1 | a0001c0002t0002g0060 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.670+3556T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221436 | ||||||
| chr13:111221436
|
T | G | 35 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(32): Show | 35 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.670+3556T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221436 | ||||||
| chr13:111221436
|
T | TATATATA others(3): Show |
6 | a0001c0002t0002g0031a0001c0002t0002g0165a0001c0002t0002g0169others(3): Show | 6 | HG00597.hp2 HG02015.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+3563_670+3564i others(12): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221436 | |||||
| chr13:111221437
|
A | ATATATGT others(250): Show |
1 | a0001c0001t0005g0126 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.670+3562_670+3563i others(259): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221437 | |||||
| chr13:111221437
|
A | ATC | 9 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017others(6): Show | 9 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.670+3558_670+3559i others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221437 | |||||
| chr13:111221438
|
T | G | 3 | a0001c0001t0002g0099a0001c0003t0003g0021a0001c0003t0019g0022 | 3 | HG02451.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.670+3558T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221438 | ||||||
| chr13:111221440
|
T | G | 79 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0047others(76): Show | 79 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.670+3560T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221440 | ||||||
| chr13:111221442
|
T | C | 36 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0047others(33): Show | 36 | HG00280.hp1 HG00639.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.670+3562T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221442 | ||||||
| chr13:111221442
|
T | TAGAC | 25 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(22): Show | 25 | HG00140.hp2 HG00639.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.670+3563_670+3564i others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221442 | |||||
| chr13:111221443
|
A | G | 11 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(8): Show | 11 | HG00558.hp1 HG01081.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.670+3563A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221443 | ||||||
| chr13:111221445
|
C | A | 5 | a0001c0001t0002g0099a0001c0003t0001g0142a0001c0003t0003g0021others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.670+3565C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221445 | ||||||
| chr13:111221446
|
T | G | 1 | a0001c0002t0002g0147 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.670+3566T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221446 | ||||||
| chr13:111221448
|
T | C | 1 | a0001c0002t0002g0147 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.670+3568T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221448 | ||||||
| chr13:111221449
|
A | ATATATCT others(69): Show |
1 | a0001c0006t0012g0124 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.670+3574_670+3575i others(78): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221449 | |||||
| chr13:111221452
|
T | G | 15 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0185others(12): Show | 15 | HG00597.hp2 HG01928.hp1 HG01943.hp2 others(12): Show |
intron_variant | MODIFIER | c.670+3572T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221452 | ||||||
| chr13:111221453
|
A | ATATC | 35 | a0001c0002t0001g0170a0001c0002t0001g0182a0001c0002t0002g0046others(32): Show | 35 | HG00323.hp2 HG01257.hp1 HG01361.hp2 others(32): Show |
intron_variant | MODIFIER | c.670+3575_670+3576i others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221453 | |||||
| chr13:111221453
|
A | ATCTATAT others(189): Show |
1 | a0001c0001t0001g0129 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.670+3574_670+3575i others(198): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221453 | |||||
| chr13:111221453
|
A | ATCTATAT others(133): Show |
1 | a0001c0001t0015g0272 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.670+3574_670+3575i others(142): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221453 | |||||
| chr13:111221453
|
A | ATCTATAT others(105): Show |
1 | a0001c0002t0002g0190 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.670+3574_670+3575i others(114): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221453 | |||||
| chr13:111221453
|
A | ATCTATAT others(77): Show |
1 | a0001c0001t0001g0137 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.670+3574_670+3575i others(86): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221453 | |||||
| chr13:111221453
|
A | ATCTATAT others(49): Show |
4 | a0001c0002t0002g0033a0001c0002t0002g0079a0001c0002t0002g0155others(1): Show | 4 | HG00558.hp1 HG03710.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+3574_670+3575i others(58): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221453 | |||||
| chr13:111221456
|
G | T | 60 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0006g0041others(57): Show | 60 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.670+3576G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221456 | ||||||
| chr13:111221457
|
A | C | 8 | a0001c0002t0002g0031a0001c0002t0002g0060a0001c0002t0002g0147others(5): Show | 8 | HG00597.hp2 HG01175.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.670+3577A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221457 | ||||||
| chr13:111221458
|
T | C | 8 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0107others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.670+3578T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221458 | ||||||
| chr13:111221461
|
A | C | 7 | a0001c0001t0006g0032a0001c0001t0006g0083a0001c0001t0006g0090others(4): Show | 7 | HG00558.hp2 HG00642.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+3581A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221461 | ||||||
| chr13:111221464
|
G | T | 24 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0107others(21): Show | 24 | HG00558.hp2 HG00597.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.670+3584G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221464 | ||||||
| chr13:111221465
|
A | C | 8 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0107others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.670+3585A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221465 | ||||||
| chr13:111221465
|
A | T | 1 | a0001c0001t0003g0024 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.670+3585A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221465 | ||||||
| chr13:111221466
|
C | T | 77 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0002g0029others(74): Show | 77 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.670+3586C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221466 | ||||||
| chr13:111221469
|
C | A | 2 | a0001c0001t0003g0024a0001c0001t0017g0270 | 2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.670+3589C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221469 | ||||||
| chr13:111221469
|
CTA | C | 3 | a0001c0001t0005g0062a0001c0001t0011g0006a0001c0001t0011g0007 | 3 | HG01884.hp1 HG02257.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.670+3598_670+3599d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221469 | |||||
| chr13:111221471
|
A | ATATAGAT others(141): Show |
8 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0185others(5): Show | 8 | HG01928.hp1 HG01943.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.670+3595_670+3596i others(150): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221471 | |||||
| chr13:111221471
|
A | C | 2 | a0001c0001t0003g0024a0001c0001t0017g0270 | 2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.670+3591A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221471 | ||||||
| chr13:111221477
|
A | C | 44 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0015g0272others(41): Show | 44 | HG00323.hp2 HG00558.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.670+3597A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221477 | ||||||
| chr13:111221478
|
TAG | T | 44 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0015g0272others(41): Show | 44 | HG00323.hp2 HG00558.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.670+3600_670+3601d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221478 | |||||
| chr13:111221479
|
A | C | 8 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0185others(5): Show | 8 | HG01928.hp1 HG01943.hp2 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.670+3599A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221479 | ||||||
| chr13:111221480
|
G | GATATATA others(7): Show |
2 | a0001c0001t0001g0125a0001c0001t0007g0057 | 2 | HG00741.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.670+3607_670+3608i others(16): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221480 | |||||
| chr13:111221480
|
G | GATATCTA others(7): Show |
13 | a0001c0001t0006g0032a0001c0001t0006g0083a0001c0001t0006g0090others(10): Show | 13 | HG00558.hp2 HG00597.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.670+3604_670+3605i others(16): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221480 | |||||
| chr13:111221480
|
G | T | 9 | a0001c0001t0006g0041a0001c0001t0006g0042a0001c0001t0006g0185others(6): Show | 9 | HG01175.hp1 HG01928.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.670+3600G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221480 | ||||||
| chr13:111221480
|
GAT | G | 17 | a0001c0001t0001g0123a0001c0001t0001g0219a0001c0001t0003g0128others(14): Show | 17 | HG00099.hp1 HG01071.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.670+3608_670+3609d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221480 | |||||
| chr13:111221488
|
T | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(49): Show | 52 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.670+3608T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221488 | ||||||
| chr13:111221488
|
TAGAC | T | 8 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0107others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.670+3610_670+3613d others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221488 | |||||
| chr13:111221490
|
G | C | 52 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(49): Show | 52 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.670+3610G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221490 | ||||||
| chr13:111221492
|
C | T | 120 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(117): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.670+3612C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221492 | ||||||
| chr13:111221492
|
CAT | C | 15 | a0001c0001t0003g0128a0001c0001t0005g0062a0001c0001t0005g0063others(12): Show | 15 | HG00741.hp1 HG01071.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.670+3621_670+3622d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221492 | |||||
| chr13:111221493
|
A | ATATATAT others(23): Show |
15 | a0001c0001t0002g0251a0001c0001t0004g0086a0001c0001t0004g0133others(12): Show | 15 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.670+3637_670+3638i others(32): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221493 | |||||
| chr13:111221493
|
A | ATATATAT others(23): Show |
16 | a0001c0001t0002g0078a0001c0001t0002g0164a0001c0001t0003g0085others(13): Show | 16 | HG01261.hp2 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.670+3632_670+3661d others(32): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221493 | |||||
| chr13:111221493
|
A | C | 60 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(57): Show | 60 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.670+3613A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221493 | ||||||
| chr13:111221493
|
A | G | 2 | a0001c0002t0021g0255a0001c0002t0021g0256 | 2 | NA18957.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.670+3613A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221493 | ||||||
| chr13:111221493
|
ATATATAT others(23): Show |
A | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.670+3632_670+3661d others(32): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221493 | |||||
| chr13:111221495
|
A | ATATATAT others(47): Show |
1 | a0001c0001t0009g0250 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.670+3631_670+3632i others(56): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221495 | |||||
| chr13:111221495
|
A | ATATATAT others(73): Show |
1 | a0001c0001t0009g0202 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.670+3631_670+3632i others(82): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221495 | |||||
| chr13:111221495
|
A | ATATATAT others(75): Show |
2 | a0001c0001t0009g0171a0001c0001t0009g0260 | 2 | NA19077.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.670+3631_670+3632i others(84): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221495 | |||||
| chr13:111221495
|
A | ATATATAT others(75): Show |
1 | a0001c0001t0009g0258 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.670+3631_670+3632i others(84): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221495 | |||||
| chr13:111221495
|
A | ATATATCT others(63): Show |
1 | a0001c0001t0003g0024 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.670+3620_670+3621i others(72): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221495 | |||||
| chr13:111221495
|
A | ATATATCT others(75): Show |
1 | a0001c0001t0029g0201 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.670+3620_670+3621i others(84): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221495 | |||||
| chr13:111221495
|
A | ATATATCT others(47): Show |
2 | a0001c0001t0009g0214a0001c0001t0009g0259 | 2 | NA19005.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.670+3620_670+3621i others(56): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221495 | |||||
| chr13:111221495
|
A | C | 53 | a0001c0001t0001g0123a0001c0001t0001g0129a0001c0001t0001g0137others(50): Show | 53 | HG00099.hp1 HG00323.hp2 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.670+3615A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221495 | ||||||
| chr13:111221498
|
T | G | 17 | a0001c0001t0001g0125a0001c0001t0006g0032a0001c0001t0006g0041others(14): Show | 17 | HG00558.hp2 HG00642.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.670+3618T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221498 | ||||||
| chr13:111221499
|
A | C | 38 | a0001c0001t0001g0051a0001c0001t0001g0173a0001c0001t0001g0200others(35): Show | 38 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.670+3619A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221499 | ||||||
| chr13:111221500
|
T | C | 17 | a0001c0001t0001g0125a0001c0001t0006g0032a0001c0001t0006g0041others(14): Show | 17 | HG00558.hp2 HG00642.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.670+3620T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221500 | ||||||
| chr13:111221502
|
T | G | 1 | a0001c0001t0034g0061 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.670+3622T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221502 | ||||||
| chr13:111221503
|
C | A | 55 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(52): Show | 55 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.670+3623C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221503 | ||||||
| chr13:111221504
|
T | G | 52 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(49): Show | 52 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.670+3624T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221504 | ||||||
| chr13:111221505
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0012g0001 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.670+3638_670+3665d others(30): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221505 | |||||
| chr13:111221505
|
ATATATAT others(21): Show |
A | 4 | a0001c0001t0001g0173a0001c0001t0001g0200a0001c0001t0001g0205others(1): Show | 4 | HG01952.hp1 HG02004.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.670+3638_670+3665d others(30): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221505 | |||||
| chr13:111221506
|
T | G | 3 | a0001c0001t0001g0123a0001c0001t0001g0219a0001c0001t0017g0270 | 3 | HG00099.hp1 HG02809.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.670+3626T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221506 | ||||||
| chr13:111221511
|
A | C | 1 | a0001c0001t0017g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.670+3631A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221511 | ||||||
| chr13:111221514
|
G | T | 1 | a0001c0001t0017g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.670+3634G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221514 | ||||||
| chr13:111221516
|
T | C | 54 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(51): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.670+3636T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221516 | ||||||
| chr13:111221518
|
T | C | 17 | a0001c0001t0001g0051a0001c0001t0001g0231a0001c0001t0001g0232others(14): Show | 17 | HG01169.hp1 NA18939.hp2 NA18941.hp2 others(14): Show |
intron_variant | MODIFIER | c.670+3638T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221518 | ||||||
| chr13:111221519
|
A | C | 1 | a0001c0002t0002g0147 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.670+3639A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221519 | ||||||
| chr13:111221520
|
T | TAGAC | 51 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(48): Show | 51 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.670+3641_670+3642i others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221520 | |||||
| chr13:111221522
|
T | G | 1 | a0001c0001t0017g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.670+3642T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221522 | ||||||
| chr13:111221522
|
T | TAGAC | 15 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(12): Show | 15 | HG00558.hp2 HG00642.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.670+3642_670+3643i others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221522 | ||||||
| chr13:111221522
|
TCTATATA others(13): Show |
T | 1 | a0001c0002t0002g0082 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.670+3643_670+3662d others(22): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221522 | ||||||
| chr13:111221523
|
C | A | 19 | a0001c0001t0001g0125a0001c0001t0006g0032a0001c0001t0006g0041others(16): Show | 19 | HG00558.hp2 HG00642.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.670+3643C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221523 | ||||||
| chr13:111221524
|
T | G | 2 | a0001c0001t0001g0125a0001c0001t0007g0057 | 2 | HG00741.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.670+3644T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221524 | ||||||
| chr13:111221524
|
T | TATATATA others(13): Show |
5 | a0001c0001t0001g0068a0001c0001t0004g0064a0001c0001t0004g0065others(2): Show | 5 | HG01167.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.670+3661_670+3662i others(22): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221524 | |||||
| chr13:111221526
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0007g0057 | 2 | HG00741.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.670+3646T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221526 | ||||||
| chr13:111221527
|
A | C | 56 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(53): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.670+3647A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221527 | ||||||
| chr13:111221529
|
ATATC | A | 53 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(50): Show | 53 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.670+3653_670+3656d others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221529 | |||||
| chr13:111221531
|
A | ATAGATAT others(9): Show |
1 | a0001c0002t0002g0046 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.670+3652_670+3653i others(18): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221531 | |||||
| chr13:111221531
|
A | C | 34 | a0001c0001t0001g0051a0001c0001t0001g0231a0001c0001t0001g0232others(31): Show | 34 | HG00558.hp2 HG00642.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.670+3651A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221531 | ||||||
| chr13:111221533
|
C | A | 87 | a0001c0001t0001g0051a0001c0001t0001g0129a0001c0001t0001g0137others(84): Show | 87 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.670+3653C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221533 | ||||||
| chr13:111221533
|
C | CTA | 34 | a0001c0001t0001g0084a0001c0001t0003g0087a0001c0001t0003g0088others(31): Show | 34 | HG00140.hp1 HG00597.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.670+3660_670+3661d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221533 | |||||
| chr13:111221533
|
C | CTATATAT others(21): Show |
2 | a0001c0001t0003g0025a0001c0001t0004g0122 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.670+3679_670+3706d others(30): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221533 | |||||
| chr13:111221534
|
T | G | 50 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(47): Show | 50 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.670+3654T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221534 | ||||||
| chr13:111221535
|
A | C | 1 | a0001c0001t0017g0270 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.670+3655A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221535 | ||||||
| chr13:111221538
|
T | G | 1 | a0001c0002t0002g0147 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.670+3658T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221538 | ||||||
| chr13:111221542
|
G | T | 52 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(49): Show | 52 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.670+3662G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221542 | ||||||
| chr13:111221544
|
T | G | 51 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(48): Show | 51 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.670+3664T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221544 | ||||||
| chr13:111221546
|
C | G | 2 | a0001c0001t0017g0270a0001c0002t0002g0147 | 2 | HG01175.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.670+3666C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221546 | ||||||
| chr13:111221546
|
C | T | 22 | a0001c0001t0002g0099a0001c0001t0006g0032a0001c0001t0006g0041others(19): Show | 22 | HG00558.hp2 HG00642.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.670+3666C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221546 | ||||||
| chr13:111221546
|
CATATCTA others(49): Show |
C | 1 | a0001c0002t0002g0157 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.670+3673_670+3728d others(58): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221546 | |||||
| chr13:111221547
|
A | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.670+3667A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221547 | ||||||
| chr13:111221548
|
T | C | 1 | a0001c0002t0002g0147 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.670+3668T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221548 | ||||||
| chr13:111221549
|
ATC | A | 50 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(47): Show | 50 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.670+3671_670+3672d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221549 | |||||
| chr13:111221551
|
C | A | 1 | a0001c0002t0002g0046 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.670+3671C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221551 | ||||||
| chr13:111221551
|
CTATATAT others(23): Show |
C | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.670+3688_670+3717d others(32): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221551 | |||||
| chr13:111221552
|
T | G | 5 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0004g0045others(2): Show | 5 | NA18939.hp2 NA18986.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+3672T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221552 | ||||||
| chr13:111221559
|
C | A | 17 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(14): Show | 17 | HG00558.hp2 HG00642.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.670+3679C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221559 | ||||||
| chr13:111221559
|
CTA | C | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.670+3688_670+3689d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221559 | |||||
| chr13:111221561
|
A | C | 16 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(13): Show | 16 | HG00558.hp2 HG00642.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.670+3681A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221561 | ||||||
| chr13:111221562
|
T | G | 1 | a0001c0002t0002g0147 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.670+3682T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221562 | ||||||
| chr13:111221570
|
G | T | 1 | a0001c0002t0002g0147 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.670+3690G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221570 | ||||||
| chr13:111221572
|
T | G | 1 | a0001c0002t0002g0147 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.670+3692T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221572 | ||||||
| chr13:111221574
|
C | CATATCTA others(1): Show |
13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.670+3699_670+3706d others(10): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221574 | |||||
| chr13:111221574
|
C | T | 53 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(50): Show | 53 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.670+3694C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221574 | ||||||
| chr13:111221574
|
CATATCTA others(21): Show |
C | 6 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017others(3): Show | 6 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+3701_670+3728d others(30): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221574 | |||||
| chr13:111221580
|
T | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.670+3700T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221580 | ||||||
| chr13:111221587
|
A | C | 70 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(67): Show | 70 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.670+3707A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221587 | ||||||
| chr13:111221589
|
C | A | 70 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(67): Show | 70 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.670+3709C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221589 | ||||||
| chr13:111221590
|
T | G | 1 | a0001c0002t0002g0189 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.670+3710T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221590 | ||||||
| chr13:111221602
|
T | C | 70 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(67): Show | 70 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.670+3722T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221602 | ||||||
| chr13:111221628
|
A | G | 77 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0001g0144others(74): Show | 77 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.670+3748A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221628 | ||||||
| chr13:111221643
|
T | TTA | 11 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.670+3776_670+3777d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221643 | |||||
| chr13:111221643
|
TTA | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.670+3776_670+3777d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221643 | |||||
| chr13:111221699
|
A | G | 40 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.670+3819A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221699 | ||||||
| chr13:111221709
|
G | GTATC | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.670+3837_670+3840d others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111221709 | |||||
| chr13:111221727
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.670+3847A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221727 | ||||||
| chr13:111221841
|
T | A | 4 | a0001c0001t0003g0178a0001c0001t0003g0216a0001c0001t0003g0262others(1): Show | 4 | HG00140.hp1 HG01099.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.670+3961T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221841 | ||||||
| chr13:111221921
|
G | A | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.670+4041G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111221921 | ||||||
| chr13:111222088
|
G | C | 15 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0097others(12): Show | 15 | HG00140.hp2 HG00642.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.670+4208G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111222088 | ||||||
| chr13:111222093
|
C | T | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.670+4213C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111222093 | ||||||
| chr13:111222118
|
G | A | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.670+4238G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111222118 | ||||||
| chr13:111222118
|
G | GCAACACC others(10): Show |
1 | a0001c0001t0007g0008 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.670+4241_670+4257d others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111222118 | |||||
| chr13:111222238
|
GAAAATTT others(32): Show |
G | 1 | a0001c0001t0001g0160 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.670+4360_670+4398d others(41): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111222238 | |||||
| chr13:111222296
|
C | A | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.670+4416C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111222296 | ||||||
| chr13:111222554
|
C | T | 1 | a0001c0005t0020g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.670+4674C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111222554 | ||||||
| chr13:111222555
|
G | A | 1 | a0001c0002t0002g0147 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.670+4675G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111222555 | ||||||
| chr13:111222921
|
A | G | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.670+5041A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111222921 | ||||||
| chr13:111223086
|
T | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.670+5206T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111223086 | ||||||
| chr13:111223113
|
T | G | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.670+5233T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111223113 | ||||||
| chr13:111223427
|
G | T | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.670+5547G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111223427 | ||||||
| chr13:111223443
|
T | C | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.670+5563T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111223443 | ||||||
| chr13:111223480
|
G | A | 220 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(217): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.670+5600G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111223480 | ||||||
| chr13:111223810
|
T | C | 6 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017others(3): Show | 6 | HG01109.hp1 HG01192.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.670+5930T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111223810 | ||||||
| chr13:111223853
|
A | G | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.670+5973A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111223853 | ||||||
| chr13:111223858
|
A | AT | 7 | a0001c0001t0001g0160a0001c0001t0001g0195a0001c0001t0003g0025others(4): Show | 7 | HG00280.hp2 HG00323.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+5994dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111223858 | |||||
| chr13:111223858
|
A | ATTT | 5 | a0001c0001t0002g0099a0001c0003t0001g0142a0001c0003t0003g0021others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.670+5992_670+5994d others(5): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111223858 | |||||
| chr13:111223858
|
AT | A | 56 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(53): Show | 56 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.670+5994delT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111223858 | |||||
| chr13:111223920
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.670+6040A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111223920 | ||||||
| chr13:111223951
|
G | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.670+6071G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111223951 | ||||||
| chr13:111224054
|
A | G | 1 | a0001c0001t0007g0094 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.670+6174A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111224054 | ||||||
| chr13:111224073
|
C | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.670+6193C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111224073 | ||||||
| chr13:111224102
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.670+6222G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111224102 | ||||||
| chr13:111224406
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.670+6526A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111224406 | ||||||
| chr13:111224653
|
T | A | 63 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.670+6773T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111224653 | ||||||
| chr13:111224838
|
T | C | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.670+6958T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111224838 | ||||||
| chr13:111225081
|
T | C | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.670+7201T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111225081 | ||||||
| chr13:111225117
|
A | G | 1 | a0001c0015t0002g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.670+7237A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111225117 | ||||||
| chr13:111225206
|
G | T | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.670+7326G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111225206 | ||||||
| chr13:111225476
|
G | A | 1 | a0001c0001t0023g0036 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.670+7596G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111225476 | ||||||
| chr13:111225512
|
G | T | 1 | a0001c0001t0019g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.670+7632G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111225512 | ||||||
| chr13:111225512
|
GT | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(4): Show | 7 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.670+7645delT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111225512 | |||||
| chr13:111225542
|
G | A | 1 | a0001c0001t0003g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.670+7662G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111225542 | ||||||
| chr13:111225561
|
G | T | 1 | a0001c0001t0004g0243 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.671-7644G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111225561 | ||||||
| chr13:111225589
|
C | G | 88 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(85): Show | 88 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.671-7616C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111225589 | ||||||
| chr13:111225935
|
G | A | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.671-7270G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111225935 | ||||||
| chr13:111226184
|
A | G | 54 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(51): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(51): Show |
intron_variant | MODIFIER | c.671-7021A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111226184 | ||||||
| chr13:111226500
|
C | T | 40 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.671-6705C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111226500 | ||||||
| chr13:111226528
|
A | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.671-6677A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111226528 | ||||||
| chr13:111227196
|
G | T | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.671-6009G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111227196 | ||||||
| chr13:111227214
|
A | G | 1 | a0001c0001t0003g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.671-5991A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111227214 | ||||||
| chr13:111227342
|
C | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.671-5863C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111227342 | ||||||
| chr13:111227439
|
C | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.671-5766C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111227439 | ||||||
| chr13:111227701
|
C | T | 5 | a0001c0001t0002g0099a0001c0003t0001g0142a0001c0003t0003g0021others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-5504C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111227701 | ||||||
| chr13:111228024
|
A | T | 5 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(2): Show | 5 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.671-5181A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111228024 | ||||||
| chr13:111228064
|
A | T | 2 | a0001c0002t0021g0255a0001c0002t0021g0256 | 2 | NA18957.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.671-5141A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111228064 | ||||||
| chr13:111228326
|
A | G | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18941.hp2 NA18962.hp2 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.671-4879A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111228326 | ||||||
| chr13:111228419
|
G | A | 8 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(5): Show | 8 | HG02559.hp1 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.671-4786G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111228419 | ||||||
| chr13:111228468
|
G | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.671-4737G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111228468 | ||||||
| chr13:111228526
|
G | A | 1 | a0001c0001t0004g0222 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.671-4679G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111228526 | ||||||
| chr13:111228619
|
G | A | 1 | a0001c0001t0008g0015 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.671-4586G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111228619 | ||||||
| chr13:111228638
|
C | T | 2 | a0001c0002t0002g0181a0001c0002t0002g0206 | 2 | HG00323.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.671-4567C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111228638 | ||||||
| chr13:111228688
|
A | G | 4 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017others(1): Show | 4 | HG01109.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.671-4517A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111228688 | ||||||
| chr13:111228696
|
G | A | 8 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(5): Show | 8 | HG02559.hp1 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.671-4509G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111228696 | ||||||
| chr13:111228704
|
G | C | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.671-4501G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111228704 | ||||||
| chr13:111228731
|
A | C | 5 | a0001c0001t0004g0122a0001c0003t0001g0142a0001c0003t0003g0021others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-4474A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111228731 | ||||||
| chr13:111228732
|
C | G | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.671-4473C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111228732 | ||||||
| chr13:111228756
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0253 | 2 | HG02735.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.671-4449A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111228756 | ||||||
| chr13:111228775
|
A | G | 1 | a0001c0001t0003g0228 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.671-4430A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111228775 | ||||||
| chr13:111229349
|
A | G | 2 | a0002c0009t0002g0069a0002c0009t0002g0112 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.671-3856A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111229349 | ||||||
| chr13:111229369
|
A | G | 2 | a0001c0001t0006g0032a0001c0001t0006g0083 | 2 | HG00558.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.671-3836A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111229369 | ||||||
| chr13:111229372
|
A | C | 78 | a0001c0001t0001g0019a0001c0001t0001g0129a0001c0001t0001g0137others(75): Show | 78 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.671-3833A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111229372 | ||||||
| chr13:111229395
|
A | G | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.671-3810A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111229395 | ||||||
| chr13:111229459
|
A | G | 1 | a0001c0001t0003g0089 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.671-3746A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111229459 | ||||||
| chr13:111229518
|
T | A | 1 | a0001c0002t0002g0082 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.671-3687T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111229518 | ||||||
| chr13:111229656
|
G | C | 5 | a0001c0001t0002g0099a0001c0003t0001g0142a0001c0003t0003g0021others(2): Show | 5 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.671-3549G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111229656 | ||||||
| chr13:111229701
|
G | C | 78 | a0001c0001t0001g0019a0001c0001t0001g0129a0001c0001t0001g0137others(75): Show | 78 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.671-3504G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111229701 | ||||||
| chr13:111229856
|
C | T | 17 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(14): Show | 17 | HG00099.hp1 HG00280.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.671-3349C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111229856 | ||||||
| chr13:111230022
|
G | A | 10 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0011g0006others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.671-3183G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111230022 | ||||||
| chr13:111230146
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0188 | 2 | HG01109.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.671-3059T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111230146 | ||||||
| chr13:111230208
|
T | C | 270 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.671-2997T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111230208 | ||||||
| chr13:111230389
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.671-2816T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111230389 | ||||||
| chr13:111230479
|
T | C | 1 | a0001c0002t0002g0257 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.671-2726T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111230479 | ||||||
| chr13:111230527
|
C | T | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.671-2678C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111230527 | ||||||
| chr13:111230546
|
G | A | 1 | a0004c0017t0003g0120 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.671-2659G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111230546 | ||||||
| chr13:111230596
|
G | A | 1 | a0001c0001t0003g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.671-2609G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111230596 | ||||||
| chr13:111230597
|
G | A | 2 | a0001c0006t0012g0121a0001c0006t0012g0124 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.671-2608G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111230597 | ||||||
| chr13:111230661
|
G | A | 2 | a0001c0001t0003g0104a0001c0001t0003g0108 | 2 | HG00099.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.671-2544G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111230661 | ||||||
| chr13:111230720
|
A | G | 112 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(109): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(109): Show |
intron_variant | MODIFIER | c.671-2485A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111230720 | ||||||
| chr13:111230742
|
C | T | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.671-2463C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111230742 | ||||||
| chr13:111230746
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0007g0057 | 2 | HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.671-2459C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111230746 | ||||||
| chr13:111230767
|
G | A | 78 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0001g0144others(75): Show | 78 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.671-2438G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111230767 | ||||||
| chr13:111230796
|
A | G | 5 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017others(2): Show | 5 | HG01109.hp1 HG01192.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.671-2409A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111230796 | ||||||
| chr13:111231087
|
C | T | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.671-2118C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111231087 | ||||||
| chr13:111231095
|
A | G | 1 | a0001c0001t0023g0037 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.671-2110A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111231095 | ||||||
| chr13:111231097
|
G | A | 1 | a0001c0001t0002g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.671-2108G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111231097 | ||||||
| chr13:111231147
|
C | T | 1 | a0001c0001t0003g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.671-2058C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111231147 | ||||||
| chr13:111231259
|
A | G | 1 | a0001c0002t0002g0190 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.671-1946A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111231259 | ||||||
| chr13:111231321
|
C | G | 6 | a0001c0001t0002g0099a0001c0001t0004g0122a0001c0003t0001g0142others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.671-1884C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111231321 | ||||||
| chr13:111231454
|
A | AACAGTGA others(27): Show |
6 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017others(3): Show | 6 | HG01109.hp1 HG01192.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.671-1729_671-1696d others(36): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111231454 | |||||
| chr13:111231521
|
C | T | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18941.hp2 NA18962.hp2 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.671-1684C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111231521 | ||||||
| chr13:111231540
|
TC | T | 10 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0011g0006others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.671-1663delC | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | 111231540 | |||||
| chr13:111231559
|
A | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | HG02698.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.671-1646A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111231559 | ||||||
| chr13:111231641
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.671-1564G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111231641 | ||||||
| chr13:111231674
|
T | A | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18941.hp2 NA18962.hp2 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.671-1531T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111231674 | ||||||
| chr13:111231711
|
G | T | 1 | a0001c0002t0002g0169 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.671-1494G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111231711 | ||||||
| chr13:111232042
|
G | A | 2 | a0002c0009t0002g0069a0002c0009t0002g0112 | 2 | HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.671-1163G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111232042 | ||||||
| chr13:111232130
|
T | C | 238 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(235): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.671-1075T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111232130 | ||||||
| chr13:111232159
|
T | C | 1 | a0001c0001t0003g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.671-1046T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111232159 | ||||||
| chr13:111232199
|
T | C | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.671-1006T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111232199 | ||||||
| chr13:111232252
|
T | C | 1 | a0001c0001t0004g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.671-953T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111232252 | ||||||
| chr13:111232311
|
T | A | 1 | a0001c0001t0003g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.671-894T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111232311 | ||||||
| chr13:111232312
|
G | C | 1 | a0001c0001t0003g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.671-893G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111232312 | ||||||
| chr13:111232313
|
T | C | 1 | a0001c0001t0003g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.671-892T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111232313 | ||||||
| chr13:111232315
|
T | C | 1 | a0001c0001t0003g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.671-890T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111232315 | ||||||
| chr13:111232316
|
G | A | 1 | a0001c0001t0003g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.671-889G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111232316 | ||||||
| chr13:111232327
|
A | G | 40 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.671-878A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111232327 | ||||||
| chr13:111232384
|
C | T | 10 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0011g0006others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.671-821C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111232384 | ||||||
| chr13:111232385
|
G | A | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.671-820G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111232385 | ||||||
| chr13:111232585
|
C | T | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.671-620C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111232585 | ||||||
| chr13:111232605
|
A | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(205): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.671-600A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111232605 | ||||||
| chr13:111232763
|
T | C | 226 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.671-442T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111232763 | ||||||
| chr13:111232872
|
C | T | 3 | a0001c0005t0020g0117a0001c0005t0020g0118a0001c0015t0002g0023 | 3 | HG01243.hp1 HG03130.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.671-333C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111232872 | ||||||
| chr13:111232953
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.671-252T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | chr13 | 111232953 | ||||||
| chr13:111233710
|
T | C | 41 | a0001c0001t0001g0084a0001c0001t0002g0029a0001c0001t0002g0156others(38): Show | 41 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(38): Show |
intron_variant | MODIFIER | c.759+417T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111233710 | ||||||
| chr13:111233743
|
A | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0096 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.759+450A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111233743 | ||||||
| chr13:111233896
|
A | T | 2 | a0001c0002t0002g0181a0001c0002t0002g0206 | 2 | HG00323.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.759+603A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111233896 | ||||||
| chr13:111234144
|
C | A | 1 | a0001c0001t0005g0212 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.759+851C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111234144 | ||||||
| chr13:111234289
|
C | T | 87 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(84): Show | 87 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.759+996C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111234289 | ||||||
| chr13:111234305
|
C | T | 1 | a0001c0001t0003g0128 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.759+1012C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111234305 | ||||||
| chr13:111234520
|
C | T | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.759+1227C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111234520 | ||||||
| chr13:111234585
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0032g0030 | 2 | HG00140.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.759+1292G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111234585 | ||||||
| chr13:111234837
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.759+1544A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111234837 | ||||||
| chr13:111234882
|
A | G | 1 | a0001c0002t0002g0031 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.759+1589A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111234882 | ||||||
| chr13:111234903
|
G | C | 1 | a0001c0002t0010g0081 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.759+1610G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111234903 | ||||||
| chr13:111235030
|
A | C | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.759+1737A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111235030 | ||||||
| chr13:111235088
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.759+1795C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111235088 | ||||||
| chr13:111235347
|
A | T | 1 | a0001c0001t0009g0214 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.759+2054A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111235347 | ||||||
| chr13:111235468
|
A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(100): Show |
intron_variant | MODIFIER | c.759+2175A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111235468 | ||||||
| chr13:111235496
|
A | C | 1 | a0001c0015t0002g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.759+2203A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111235496 | ||||||
| chr13:111235959
|
G | A | 10 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0051others(7): Show | 10 | HG00099.hp1 HG00280.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.759+2666G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111235959 | ||||||
| chr13:111235980
|
G | A | 1 | a0001c0002t0002g0149 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.759+2687G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111235980 | ||||||
| chr13:111235982
|
G | A | 2 | a0001c0002t0002g0151a0001c0002t0002g0152 | 2 | NA18941.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.759+2689G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111235982 | ||||||
| chr13:111236024
|
A | G | 1 | a0001c0001t0004g0254 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.759+2731A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111236024 | ||||||
| chr13:111236114
|
T | C | 1 | a0001c0002t0010g0080 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.759+2821T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111236114 | ||||||
| chr13:111236479
|
T | A | 225 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.759+3186T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111236479 | ||||||
| chr13:111236533
|
T | G | 1 | a0001c0001t0015g0272 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.759+3240T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111236533 | ||||||
| chr13:111236735
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.759+3442G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111236735 | ||||||
| chr13:111236975
|
A | T | 40 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.759+3682A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111236975 | ||||||
| chr13:111237178
|
C | A | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.759+3885C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111237178 | ||||||
| chr13:111237336
|
A | G | 8 | a0001c0001t0009g0171a0001c0001t0009g0202a0001c0001t0009g0214others(5): Show | 8 | NA18941.hp2 NA18962.hp2 NA18982.hp1 others(5): Show |
intron_variant | MODIFIER | c.759+4043A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111237336 | ||||||
| chr13:111237649
|
G | A | 10 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0011g0006others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.759+4356G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111237649 | ||||||
| chr13:111238166
|
T | C | 18 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0097others(15): Show | 18 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.759+4873T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111238166 | ||||||
| chr13:111238209
|
C | T | 76 | a0001c0001t0001g0019a0001c0001t0001g0129a0001c0001t0001g0137others(73): Show | 76 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.759+4916C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111238209 | ||||||
| chr13:111238439
|
A | T | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.759+5146A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111238439 | ||||||
| chr13:111238468
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0253 | 2 | HG02735.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.759+5175A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111238468 | ||||||
| chr13:111238807
|
T | A | 19 | a0001c0001t0001g0040a0001c0001t0001g0047a0001c0001t0001g0049others(16): Show | 19 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.760-5065T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111238807 | ||||||
| chr13:111238902
|
C | T | 14 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(11): Show | 14 | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.760-4970C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111238902 | ||||||
| chr13:111238952
|
G | A | 227 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(224): Show | 227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.760-4920G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111238952 | ||||||
| chr13:111239072
|
T | C | 1 | a0001c0001t0004g0239 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.760-4800T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111239072 | ||||||
| chr13:111239109
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.760-4763C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111239109 | ||||||
| chr13:111239140
|
C | T | 4 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0023g0036others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.760-4732C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111239140 | ||||||
| chr13:111239172
|
C | T | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.760-4700C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111239172 | ||||||
| chr13:111239331
|
C | T | 1 | a0001c0001t0001g0047 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.760-4541C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111239331 | ||||||
| chr13:111239336
|
A | G | 2 | a0001c0001t0001g0093a0001c0001t0012g0013 | 2 | HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.760-4536A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111239336 | ||||||
| chr13:111239493
|
C | T | 1 | a0001c0001t0001g0220 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.760-4379C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111239493 | ||||||
| chr13:111239581
|
A | G | 1 | a0001c0001t0025g0176 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.760-4291A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111239581 | ||||||
| chr13:111239839
|
C | T | 1 | a0001c0001t0013g0154 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.760-4033C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111239839 | ||||||
| chr13:111239840
|
G | A | 8 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(5): Show | 8 | HG02559.hp1 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.760-4032G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111239840 | ||||||
| chr13:111239890
|
G | C | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.760-3982G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111239890 | ||||||
| chr13:111239952
|
G | A | 2 | a0001c0002t0002g0046a0001c0002t0002g0199 | 2 | NA18988.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.760-3920G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111239952 | ||||||
| chr13:111239975
|
C | A | 8 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(5): Show | 8 | HG02559.hp1 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.760-3897C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111239975 | ||||||
| chr13:111239975
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.760-3897C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111239975 | ||||||
| chr13:111240039
|
T | C | 1 | a0001c0001t0003g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.760-3833T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111240039 | ||||||
| chr13:111240047
|
C | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(61): Show | 64 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.760-3825C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111240047 | ||||||
| chr13:111240171
|
G | A | 1 | a0001c0007t0004g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.760-3701G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111240171 | ||||||
| chr13:111240274
|
G | A | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.760-3598G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111240274 | ||||||
| chr13:111240299
|
A | G | 19 | a0001c0001t0001g0040a0001c0001t0001g0047a0001c0001t0001g0049others(16): Show | 19 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.760-3573A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111240299 | ||||||
| chr13:111240371
|
A | G | 1 | a0001c0001t0003g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.760-3501A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111240371 | ||||||
| chr13:111240373
|
C | CT | 7 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017others(4): Show | 7 | HG01109.hp1 HG01192.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.760-3492dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr13 | 111240373 | |||||
| chr13:111240541
|
C | T | 2 | a0001c0001t0029g0201a0001c0005t0020g0117 | 2 | HG01243.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.760-3331C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111240541 | ||||||
| chr13:111240622
|
T | C | 9 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0066others(6): Show | 9 | HG02647.hp2 HG03195.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.760-3250T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111240622 | ||||||
| chr13:111240663
|
A | G | 12 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0003g0025others(9): Show | 12 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.760-3209A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111240663 | ||||||
| chr13:111240690
|
T | C | 1 | a0001c0001t0003g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.760-3182T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111240690 | ||||||
| chr13:111240701
|
A | G | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.760-3171A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111240701 | ||||||
| chr13:111240706
|
A | G | 4 | a0001c0001t0016g0143a0001c0001t0019g0071a0001c0005t0020g0117others(1): Show | 4 | HG01243.hp1 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.760-3166A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111240706 | ||||||
| chr13:111240825
|
C | T | 4 | a0001c0001t0029g0201a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18941.hp2 NA18957.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.760-3047C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111240825 | ||||||
| chr13:111240941
|
A | G | 4 | a0001c0001t0003g0178a0001c0001t0003g0216a0001c0001t0003g0262others(1): Show | 4 | HG00140.hp1 HG01099.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.760-2931A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111240941 | ||||||
| chr13:111241002
|
G | A | 2 | a0001c0001t0003g0024a0001c0001t0017g0270 | 2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.760-2870G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111241002 | ||||||
| chr13:111241022
|
C | T | 10 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0011g0006others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.760-2850C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111241022 | ||||||
| chr13:111241023
|
G | A | 1 | a0006c0019t0002g0175 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.760-2849G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111241023 | ||||||
| chr13:111241066
|
C | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(61): Show | 64 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.760-2806C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111241066 | ||||||
| chr13:111241362
|
C | T | 53 | a0001c0001t0001g0019a0001c0001t0001g0129a0001c0001t0001g0137others(50): Show | 53 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.760-2510C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111241362 | ||||||
| chr13:111241363
|
G | A | 36 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(33): Show | 36 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.760-2509G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111241363 | ||||||
| chr13:111241618
|
T | C | 1 | a0001c0001t0003g0145 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.760-2254T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111241618 | ||||||
| chr13:111241703
|
G | A | 4 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017others(1): Show | 4 | HG01109.hp1 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.760-2169G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111241703 | ||||||
| chr13:111241916
|
C | G | 1 | a0001c0001t0001g0229 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.760-1956C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111241916 | ||||||
| chr13:111241947
|
T | C | 234 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.760-1925T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111241947 | ||||||
| chr13:111242216
|
G | T | 1 | a0001c0001t0008g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.760-1656G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111242216 | ||||||
| chr13:111242257
|
A | G | 3 | a0001c0001t0003g0107a0001c0001t0003g0136a0001c0001t0003g0215 | 3 | HG01891.hp2 HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.760-1615A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111242257 | ||||||
| chr13:111242324
|
G | T | 32 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(29): Show | 32 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.760-1548G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111242324 | ||||||
| chr13:111242329
|
G | A | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.760-1543G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111242329 | ||||||
| chr13:111242333
|
C | T | 32 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(29): Show | 32 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.760-1539C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111242333 | ||||||
| chr13:111242412
|
A | G | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.760-1460A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111242412 | ||||||
| chr13:111242478
|
T | C | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.760-1394T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111242478 | ||||||
| chr13:111242535
|
A | G | 9 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0003g0025others(6): Show | 9 | HG00741.hp1 HG01081.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.760-1337A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111242535 | ||||||
| chr13:111242881
|
G | A | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.760-991G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111242881 | ||||||
| chr13:111242984
|
A | G | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.760-888A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111242984 | ||||||
| chr13:111243017
|
G | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.760-855G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111243017 | ||||||
| chr13:111243103
|
A | G | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.760-769A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111243103 | ||||||
| chr13:111243229
|
GT | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(61): Show | 64 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.760-636delT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr13 | 111243229 | |||||
| chr13:111243389
|
T | C | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.760-483T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111243389 | ||||||
| chr13:111243399
|
C | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(61): Show | 64 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(61): Show |
intron_variant | MODIFIER | c.760-473C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111243399 | ||||||
| chr13:111243422
|
CTT | C | 3 | a0001c0001t0011g0006a0001c0001t0011g0007a0001c0001t0011g0075 | 3 | HG01884.hp1 HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.760-449_760-448del others(2): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111243422 | ||||||
| chr13:111243466
|
G | A | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.760-406G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111243466 | ||||||
| chr13:111243644
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.760-228A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 6/21 | chr13 | 111243644 | ||||||
| chr13:111244330
|
T | G | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.950+36T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111244330 | ||||||
| chr13:111244514
|
A | G | 4 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0023g0036others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.950+220A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111244514 | ||||||
| chr13:111244686
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.950+392T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111244686 | ||||||
| chr13:111244756
|
G | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.950+462G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111244756 | ||||||
| chr13:111244871
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.950+577G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111244871 | ||||||
| chr13:111244963
|
C | T | 1 | a0001c0015t0002g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.950+669C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111244963 | ||||||
| chr13:111244984
|
A | C | 2 | a0001c0001t0008g0035a0001c0016t0008g0227 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.950+690A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111244984 | ||||||
| chr13:111245016
|
A | G | 273 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.950+722A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111245016 | ||||||
| chr13:111245095
|
G | A | 29 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0085others(26): Show | 29 | HG00099.hp2 HG00597.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.950+801G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111245095 | ||||||
| chr13:111245175
|
G | A | 1 | a0001c0015t0002g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.950+881G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111245175 | ||||||
| chr13:111245327
|
G | C | 53 | a0001c0001t0001g0019a0001c0001t0001g0129a0001c0001t0001g0137others(50): Show | 53 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.950+1033G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111245327 | ||||||
| chr13:111245383
|
T | C | 14 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(11): Show | 14 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.950+1089T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111245383 | ||||||
| chr13:111245386
|
T | C | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.950+1092T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111245386 | ||||||
| chr13:111245408
|
A | G | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.950+1114A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111245408 | ||||||
| chr13:111245501
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.950+1207G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111245501 | ||||||
| chr13:111245537
|
T | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(123): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.950+1243T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111245537 | ||||||
| chr13:111245612
|
G | A | 4 | a0001c0001t0003g0178a0001c0001t0003g0216a0001c0001t0003g0262others(1): Show | 4 | HG00140.hp1 HG01099.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.950+1318G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111245612 | ||||||
| chr13:111245875
|
T | C | 7 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0003g0025others(4): Show | 7 | HG01109.hp1 HG01192.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.950+1581T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111245875 | ||||||
| chr13:111246137
|
A | T | 1 | a0001c0002t0010g0197 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.950+1843A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111246137 | ||||||
| chr13:111246139
|
T | A | 1 | a0001c0002t0010g0197 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.950+1845T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111246139 | ||||||
| chr13:111246142
|
C | T | 1 | a0001c0002t0010g0197 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.950+1848C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111246142 | ||||||
| chr13:111246150
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0007g0057 | 2 | HG03195.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.950+1856G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111246150 | ||||||
| chr13:111246385
|
G | T | 1 | a0001c0001t0001g0047 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.950+2091G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111246385 | ||||||
| chr13:111246438
|
A | G | 21 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(18): Show | 21 | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.950+2144A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111246438 | ||||||
| chr13:111246591
|
C | G | 1 | a0001c0001t0007g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.950+2297C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111246591 | ||||||
| chr13:111246743
|
A | G | 3 | a0001c0001t0001g0043a0001c0001t0001g0052a0001c0001t0003g0274 | 3 | HG03492.hp2 HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.950+2449A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111246743 | ||||||
| chr13:111247063
|
T | A | 1 | a0001c0001t0001g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.950+2769T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111247063 | ||||||
| chr13:111247065
|
C | T | 10 | a0001c0001t0001g0092a0001c0001t0001g0097a0001c0001t0001g0125others(7): Show | 10 | HG00140.hp2 HG00642.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.950+2771C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111247065 | ||||||
| chr13:111247190
|
G | A | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.950+2896G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111247190 | ||||||
| chr13:111247253
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.950+2959G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111247253 | ||||||
| chr13:111247273
|
C | CT | 62 | a0001c0001t0001g0084a0001c0001t0002g0029a0001c0001t0002g0156others(59): Show | 62 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.950+2992dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111247273 | |||||
| chr13:111247413
|
C | T | 38 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(35): Show | 38 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.950+3119C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111247413 | ||||||
| chr13:111247484
|
T | C | 1 | a0001c0002t0002g0204 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.950+3190T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111247484 | ||||||
| chr13:111247562
|
C | T | 1 | a0001c0002t0002g0181 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.950+3268C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111247562 | ||||||
| chr13:111247593
|
A | AT | 10 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0011g0006others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.950+3310dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111247593 | |||||
| chr13:111247614
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.950+3320A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111247614 | ||||||
| chr13:111247729
|
A | G | 1 | a0001c0001t0003g0266 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.950+3435A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111247729 | ||||||
| chr13:111247959
|
A | G | 8 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(5): Show | 8 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.950+3665A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111247959 | ||||||
| chr13:111247985
|
A | C | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.950+3691A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111247985 | ||||||
| chr13:111248041
|
T | C | 21 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(18): Show | 21 | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.950+3747T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111248041 | ||||||
| chr13:111248063
|
A | C | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.950+3769A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111248063 | ||||||
| chr13:111248073
|
A | G | 2 | a0001c0001t0004g0133a0001c0001t0004g0134 | 2 | NA19066.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.950+3779A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111248073 | ||||||
| chr13:111248086
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.950+3792T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111248086 | ||||||
| chr13:111248151
|
T | A | 1 | a0001c0001t0002g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.950+3857T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111248151 | ||||||
| chr13:111248217
|
C | T | 1 | a0001c0005t0020g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.950+3923C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111248217 | ||||||
| chr13:111248371
|
C | T | 1 | a0001c0012t0030g0072 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.950+4077C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111248371 | ||||||
| chr13:111248393
|
C | A | 53 | a0001c0001t0001g0019a0001c0001t0001g0129a0001c0001t0001g0137others(50): Show | 53 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.950+4099C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111248393 | ||||||
| chr13:111248436
|
C | T | 1 | a0001c0001t0006g0042 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.950+4142C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111248436 | ||||||
| chr13:111248499
|
TAC | T | 10 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0011g0006others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.950+4208_950+4209d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111248499 | |||||
| chr13:111248586
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.950+4292C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111248586 | ||||||
| chr13:111248762
|
T | G | 59 | a0001c0001t0001g0019a0001c0001t0001g0084a0001c0001t0001g0129others(56): Show | 59 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.950+4468T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111248762 | ||||||
| chr13:111249001
|
T | C | 3 | a0001c0001t0005g0139a0001c0001t0005g0140a0001c0001t0005g0141 | 3 | HG01257.hp2 HG01361.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.950+4707T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111249001 | ||||||
| chr13:111249207
|
C | G | 1 | a0001c0002t0002g0206 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.950+4913C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111249207 | ||||||
| chr13:111249209
|
A | C | 4 | a0001c0001t0004g0238a0001c0001t0004g0239a0001c0001t0004g0241others(1): Show | 4 | HG00738.hp2 HG02135.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.950+4915A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111249209 | ||||||
| chr13:111249261
|
T | C | 1 | a0001c0001t0017g0269 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.950+4967T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111249261 | ||||||
| chr13:111249335
|
A | G | 1 | a0006c0019t0002g0175 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.950+5041A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111249335 | ||||||
| chr13:111249350
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0219 | 2 | HG00099.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.950+5056C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111249350 | ||||||
| chr13:111249556
|
G | T | 1 | a0001c0002t0010g0080 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.950+5262G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111249556 | ||||||
| chr13:111249572
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.950+5278G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111249572 | ||||||
| chr13:111249677
|
T | G | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.950+5383T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111249677 | ||||||
| chr13:111249815
|
C | T | 1 | a0001c0001t0004g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.950+5521C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111249815 | ||||||
| chr13:111249888
|
G | A | 9 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(6): Show | 9 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.950+5594G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111249888 | ||||||
| chr13:111250002
|
A | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0129a0001c0001t0001g0137others(1): Show | 4 | HG02145.hp2 HG02717.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.950+5708A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111250002 | ||||||
| chr13:111250069
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.950+5775C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111250069 | ||||||
| chr13:111250126
|
C | T | 5 | a0001c0001t0001g0084a0001c0001t0001g0144a0001c0001t0002g0011others(2): Show | 5 | HG01109.hp1 HG02886.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.950+5832C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111250126 | ||||||
| chr13:111250135
|
A | T | 1 | a0001c0001t0018g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.950+5841A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111250135 | ||||||
| chr13:111250204
|
A | G | 1 | a0001c0001t0004g0241 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.950+5910A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111250204 | ||||||
| chr13:111250347
|
C | T | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.950+6053C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111250347 | ||||||
| chr13:111250523
|
A | G | 69 | a0001c0001t0001g0019a0001c0001t0001g0129a0001c0001t0001g0137others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.950+6229A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111250523 | ||||||
| chr13:111250594
|
A | G | 9 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(6): Show | 9 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.950+6300A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111250594 | ||||||
| chr13:111250883
|
A | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.950+6589A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111250883 | ||||||
| chr13:111250899
|
C | A | 1 | a0001c0001t0005g0116 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.950+6605C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111250899 | ||||||
| chr13:111251226
|
A | G | 9 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(6): Show | 9 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.950+6932A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111251226 | ||||||
| chr13:111251351
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.950+7057G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111251351 | ||||||
| chr13:111251396
|
A | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0096 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.950+7102A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111251396 | ||||||
| chr13:111251650
|
T | C | 6 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(3): Show | 6 | HG00741.hp1 HG01081.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.950+7356T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111251650 | ||||||
| chr13:111251687
|
A | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.950+7393A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111251687 | ||||||
| chr13:111251846
|
C | T | 1 | a0001c0001t0001g0014 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.950+7552C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111251846 | ||||||
| chr13:111251852
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.950+7558C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111251852 | ||||||
| chr13:111252113
|
T | C | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.950+7819T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111252113 | ||||||
| chr13:111252122
|
A | G | 6 | a0001c0001t0001g0084a0001c0001t0001g0144a0001c0001t0002g0011others(3): Show | 6 | HG01109.hp1 HG01192.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.950+7828A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111252122 | ||||||
| chr13:111252317
|
C | T | 1 | a0001c0002t0010g0081 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.950+8023C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111252317 | ||||||
| chr13:111252324
|
T | A | 9 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(6): Show | 9 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.950+8030T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111252324 | ||||||
| chr13:111252334
|
A | G | 1 | a0001c0001t0008g0035 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.950+8040A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111252334 | ||||||
| chr13:111252455
|
G | A | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.950+8161G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111252455 | ||||||
| chr13:111252486
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(4): Show | 7 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.950+8192G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111252486 | ||||||
| chr13:111252653
|
C | T | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.950+8359C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111252653 | ||||||
| chr13:111252913
|
G | A | 1 | a0001c0001t0012g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.950+8619G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111252913 | ||||||
| chr13:111252977
|
C | T | 149 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.950+8683C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111252977 | ||||||
| chr13:111253008
|
C | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.950+8714C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111253008 | ||||||
| chr13:111253019
|
C | T | 2 | a0001c0006t0012g0121a0001c0006t0012g0124 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.950+8725C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111253019 | ||||||
| chr13:111253081
|
G | T | 1 | a0001c0001t0001g0173 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.950+8787G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111253081 | ||||||
| chr13:111253085
|
C | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.950+8791C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111253085 | ||||||
| chr13:111253180
|
G | A | 10 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0011g0006others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.950+8886G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111253180 | ||||||
| chr13:111253200
|
T | C | 3 | a0001c0001t0004g0242a0001c0001t0004g0243a0001c0001t0006g0246 | 3 | NA18968.hp1 NA18971.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.950+8906T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111253200 | ||||||
| chr13:111253361
|
G | T | 1 | a0001c0001t0006g0246 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.950+9067G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111253361 | ||||||
| chr13:111253632
|
T | C | 2 | a0001c0002t0001g0170a0001c0002t0024g0183 | 2 | HG01257.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.950+9338T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111253632 | ||||||
| chr13:111253667
|
T | C | 4 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0003g0025others(1): Show | 4 | HG01109.hp1 HG02886.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.950+9373T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111253667 | ||||||
| chr13:111253677
|
C | T | 1 | a0001c0001t0004g0064 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.950+9383C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111253677 | ||||||
| chr13:111253697
|
T | A | 1 | a0001c0001t0006g0246 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.950+9403T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111253697 | ||||||
| chr13:111253718
|
T | A | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.950+9424T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111253718 | ||||||
| chr13:111254108
|
G | C | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.950+9814G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254108 | ||||||
| chr13:111254250
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.950+9956G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254250 | ||||||
| chr13:111254265
|
G | A | 1 | a0001c0007t0004g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.950+9971G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254265 | ||||||
| chr13:111254301
|
C | A | 1 | a0001c0001t0001g0168 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.950+10007C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254301 | ||||||
| chr13:111254323
|
T | G | 1 | a0001c0001t0005g0115 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.950+10029T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254323 | ||||||
| chr13:111254361
|
CCACTAAC others(44): Show |
C | 202 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.950+10120_950+1017 others(55): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111254361 | |||||
| chr13:111254380
|
GCTCAGAA others(95): Show |
G | 7 | a0001c0001t0005g0126a0001c0003t0001g0142a0001c0003t0003g0021others(4): Show | 7 | HG00741.hp1 HG01081.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.950+10120_950+1022 others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111254380 | |||||
| chr13:111254382
|
T | C | 1 | a0001c0005t0020g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.950+10088T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254382 | ||||||
| chr13:111254406
|
G | A | 25 | a0001c0001t0001g0093a0001c0001t0003g0215a0001c0001t0003g0240others(22): Show | 25 | HG00558.hp2 HG00597.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.950+10112G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254406 | ||||||
| chr13:111254414
|
A | G | 26 | a0001c0001t0001g0093a0001c0001t0003g0215a0001c0001t0003g0240others(23): Show | 26 | HG00558.hp2 HG00597.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.950+10120A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254414 | ||||||
| chr13:111254420
|
A | G | 1 | a0001c0005t0020g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.950+10126A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254420 | ||||||
| chr13:111254431
|
G | C | 25 | a0001c0001t0001g0093a0001c0001t0003g0215a0001c0001t0003g0240others(22): Show | 25 | HG00558.hp2 HG00597.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.950+10137G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254431 | ||||||
| chr13:111254431
|
GCTCAGAA others(146): Show |
G | 1 | a0001c0005t0020g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.950+10177_950+1032 others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111254431 | |||||
| chr13:111254457
|
G | A | 202 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(199): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.950+10163G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254457 | ||||||
| chr13:111254465
|
G | A | 25 | a0001c0001t0001g0093a0001c0001t0003g0215a0001c0001t0003g0240others(22): Show | 25 | HG00558.hp2 HG00597.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.950+10171G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254465 | ||||||
| chr13:111254482
|
C | G | 25 | a0001c0001t0001g0093a0001c0001t0003g0215a0001c0001t0003g0240others(22): Show | 25 | HG00558.hp2 HG00597.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.950+10188C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254482 | ||||||
| chr13:111254508
|
G | A | 7 | a0001c0001t0005g0126a0001c0003t0001g0142a0001c0003t0003g0021others(4): Show | 7 | HG00741.hp1 HG01081.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.950+10214G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254508 | ||||||
| chr13:111254516
|
G | A | 226 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(223): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.950+10222G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254516 | ||||||
| chr13:111254522
|
A | G | 35 | a0001c0001t0001g0093a0001c0001t0003g0215a0001c0001t0003g0240others(32): Show | 35 | HG00558.hp2 HG00597.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.950+10228A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254522 | ||||||
| chr13:111254530
|
C | T | 25 | a0001c0001t0001g0093a0001c0001t0003g0215a0001c0001t0003g0240others(22): Show | 25 | HG00558.hp2 HG00597.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.950+10236C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254530 | ||||||
| chr13:111254533
|
G | C | 30 | a0001c0001t0001g0093a0001c0001t0003g0215a0001c0001t0003g0240others(27): Show | 30 | HG00558.hp2 HG00597.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.950+10239G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254533 | ||||||
| chr13:111254539
|
A | G | 1 | a0001c0001t0007g0008 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.950+10245A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254539 | ||||||
| chr13:111254567
|
A | G | 31 | a0001c0001t0001g0093a0001c0001t0002g0251a0001c0001t0003g0215others(28): Show | 31 | HG00558.hp2 HG00597.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.950+10273A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254567 | ||||||
| chr13:111254572
|
C | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.950+10278C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254572 | ||||||
| chr13:111254581
|
T | C | 26 | a0001c0001t0001g0093a0001c0001t0003g0215a0001c0001t0003g0240others(23): Show | 26 | HG00558.hp2 HG00597.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.950+10287T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254581 | ||||||
| chr13:111254584
|
C | G | 25 | a0001c0001t0001g0093a0001c0001t0003g0215a0001c0001t0003g0240others(22): Show | 25 | HG00558.hp2 HG00597.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.950+10290C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254584 | ||||||
| chr13:111254586
|
T | C | 26 | a0001c0001t0001g0093a0001c0001t0003g0215a0001c0001t0003g0240others(23): Show | 26 | HG00558.hp2 HG00597.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.950+10292T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254586 | ||||||
| chr13:111254586
|
T | TCAGAAGA others(44): Show |
1 | a0001c0001t0002g0251 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.950+10853_950+1090 others(55): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111254586 | |||||
| chr13:111254586
|
TCAGAAGA others(44): Show |
T | 21 | a0001c0001t0001g0084a0001c0001t0001g0144a0001c0001t0002g0011others(18): Show | 21 | HG00280.hp2 HG00323.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.950+10853_950+1090 others(55): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111254586 | |||||
| chr13:111254586
|
TCAGAAGA others(95): Show |
T | 47 | a0001c0001t0016g0143a0001c0002t0001g0170a0001c0002t0001g0182others(44): Show | 47 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.950+10802_950+1090 others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111254586 | |||||
| chr13:111254586
|
TCAGAAGA others(146): Show |
T | 2 | a0001c0001t0005g0063a0001c0001t0005g0126 | 2 | HG01175.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.950+10751_950+1090 others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111254586 | |||||
| chr13:111254586
|
TCAGAAGA others(197): Show |
T | 8 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(5): Show | 8 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.950+10700_950+1090 others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111254586 | |||||
| chr13:111254592
|
G | C | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.950+10298G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254592 | ||||||
| chr13:111254632
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.950+10338C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254632 | ||||||
| chr13:111254650
|
C | T | 1 | a0001c0005t0020g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.950+10356C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254650 | ||||||
| chr13:111254660
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0012g0013 | 2 | HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.950+10366C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254660 | ||||||
| chr13:111254684
|
G | T | 19 | a0001c0001t0001g0040a0001c0001t0001g0047a0001c0001t0001g0049others(16): Show | 19 | HG00639.hp1 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.950+10390G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254684 | ||||||
| chr13:111254711
|
C | T | 13 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(10): Show | 13 | HG00099.hp1 HG00280.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.950+10417C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254711 | ||||||
| chr13:111254822
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.950+10528G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254822 | ||||||
| chr13:111254839
|
GCCCAGAA others(45): Show |
G | 1 | a0001c0001t0006g0246 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.950+10548_950+1059 others(56): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111254839 | |||||
| chr13:111254865
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.950+10571G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254865 | ||||||
| chr13:111254906
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.950+10612G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254906 | ||||||
| chr13:111254941
|
G | C | 21 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(18): Show | 21 | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.950+10647G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254941 | ||||||
| chr13:111254943
|
C | T | 21 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(18): Show | 21 | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.950+10649C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254943 | ||||||
| chr13:111254954
|
T | A | 1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.950+10660T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254954 | ||||||
| chr13:111254992
|
G | C | 165 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.950+10698G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254992 | ||||||
| chr13:111254994
|
C | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(162): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.950+10700C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111254994 | ||||||
| chr13:111255007
|
C | T | 1 | a0001c0005t0020g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.950+10713C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255007 | ||||||
| chr13:111255064
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.950+10770A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255064 | ||||||
| chr13:111255094
|
G | C | 68 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(65): Show | 68 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.950+10800G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255094 | ||||||
| chr13:111255096
|
C | T | 68 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(65): Show | 68 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.950+10802C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255096 | ||||||
| chr13:111255115
|
A | G | 3 | a0001c0001t0008g0015a0001c0001t0008g0035a0001c0016t0008g0227 | 3 | HG02818.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.950+10821A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255115 | ||||||
| chr13:111255119
|
C | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.950+10825C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255119 | ||||||
| chr13:111255128
|
G | A | 21 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(18): Show | 21 | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.950+10834G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255128 | ||||||
| chr13:111255134
|
G | A | 21 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(18): Show | 21 | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.950+10840G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255134 | ||||||
| chr13:111255142
|
C | T | 4 | a0001c0001t0001g0016a0001c0001t0001g0066a0001c0001t0001g0074others(1): Show | 4 | HG01123.hp2 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.950+10848C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255142 | ||||||
| chr13:111255147
|
C | T | 21 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(18): Show | 21 | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.950+10853C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255147 | ||||||
| chr13:111255179
|
G | A | 21 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(18): Show | 21 | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.950+10885G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255179 | ||||||
| chr13:111255193
|
C | T | 21 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(18): Show | 21 | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.950+10899C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255193 | ||||||
| chr13:111255196
|
G | C | 21 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(18): Show | 21 | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.950+10902G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255196 | ||||||
| chr13:111255398
|
T | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.950+11104T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255398 | ||||||
| chr13:111255478
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.950+11184A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255478 | ||||||
| chr13:111255495
|
C | T | 3 | a0001c0001t0003g0107a0001c0001t0003g0136a0001c0001t0003g0215 | 3 | HG01891.hp2 HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.950+11201C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255495 | ||||||
| chr13:111255531
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.950+11237G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255531 | ||||||
| chr13:111255738
|
A | C | 2 | a0001c0001t0015g0271a0001c0001t0015g0273 | 2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.950+11444A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255738 | ||||||
| chr13:111255773
|
A | G | 1 | a0001c0001t0006g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.950+11479A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255773 | ||||||
| chr13:111255831
|
C | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.950+11537C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255831 | ||||||
| chr13:111255962
|
T | C | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-11586T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111255962 | ||||||
| chr13:111256097
|
A | G | 3 | a0001c0001t0016g0012a0001c0001t0016g0077a0001c0012t0030g0072 | 3 | HG02280.hp2 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.951-11451A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111256097 | ||||||
| chr13:111256202
|
A | G | 1 | a0001c0001t0004g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.951-11346A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111256202 | ||||||
| chr13:111256203
|
A | C | 1 | a0001c0001t0004g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.951-11345A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111256203 | ||||||
| chr13:111256544
|
C | G | 1 | a0001c0001t0002g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.951-11004C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111256544 | ||||||
| chr13:111256644
|
C | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(2): Show | 5 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.951-10904C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111256644 | ||||||
| chr13:111256700
|
T | G | 1 | a0001c0001t0009g0214 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.951-10848T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111256700 | ||||||
| chr13:111256903
|
A | G | 5 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(2): Show | 5 | HG01192.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.951-10645A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111256903 | ||||||
| chr13:111256983
|
A | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-10565A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111256983 | ||||||
| chr13:111257183
|
A | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-10365A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111257183 | ||||||
| chr13:111257230
|
C | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-10318C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111257230 | ||||||
| chr13:111257329
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-10219A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111257329 | ||||||
| chr13:111257637
|
C | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-9911C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111257637 | ||||||
| chr13:111257704
|
T | C | 1 | a0001c0001t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.951-9844T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111257704 | ||||||
| chr13:111257834
|
C | T | 1 | a0001c0001t0003g0215 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.951-9714C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111257834 | ||||||
| chr13:111257945
|
G | A | 52 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(49): Show | 52 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.951-9603G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111257945 | ||||||
| chr13:111258088
|
G | A | 42 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0085others(39): Show | 42 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.951-9460G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111258088 | ||||||
| chr13:111258091
|
G | A | 1 | a0001c0001t0003g0184 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.951-9457G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111258091 | ||||||
| chr13:111258251
|
A | G | 1 | a0001c0005t0020g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.951-9297A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111258251 | ||||||
| chr13:111258273
|
G | A | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.951-9275G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111258273 | ||||||
| chr13:111258381
|
C | T | 3 | a0001c0002t0021g0255a0001c0002t0021g0256a0001c0002t0031g0130 | 3 | NA18957.hp1 NA18979.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.951-9167C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111258381 | ||||||
| chr13:111258613
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-8935A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111258613 | ||||||
| chr13:111258689
|
C | CCTT | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-8857_951-8856i others(5): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111258689 | |||||
| chr13:111258907
|
T | C | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.951-8641T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111258907 | ||||||
| chr13:111258958
|
C | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-8590C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111258958 | ||||||
| chr13:111259117
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.951-8431G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111259117 | ||||||
| chr13:111259121
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.951-8427A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111259121 | ||||||
| chr13:111259152
|
A | G | 5 | a0001c0001t0004g0222a0001c0001t0004g0223a0001c0001t0004g0224others(2): Show | 5 | HG01261.hp2 HG02109.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.951-8396A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111259152 | ||||||
| chr13:111259205
|
C | T | 4 | a0001c0001t0029g0201a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18941.hp2 NA18957.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.951-8343C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111259205 | ||||||
| chr13:111259206
|
C | T | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.951-8342C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111259206 | ||||||
| chr13:111259209
|
T | G | 4 | a0001c0001t0029g0201a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18941.hp2 NA18957.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.951-8339T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111259209 | ||||||
| chr13:111259240
|
G | A | 52 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(49): Show | 52 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.951-8308G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111259240 | ||||||
| chr13:111259264
|
A | G | 2 | a0001c0001t0006g0032a0001c0001t0006g0083 | 2 | HG00558.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.951-8284A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111259264 | ||||||
| chr13:111259447
|
A | G | 10 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.951-8101A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111259447 | ||||||
| chr13:111259652
|
G | A | 1 | a0001c0001t0007g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.951-7896G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111259652 | ||||||
| chr13:111259713
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.951-7835C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111259713 | ||||||
| chr13:111259746
|
C | T | 2 | a0001c0002t0002g0181a0001c0002t0002g0206 | 2 | HG00323.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.951-7802C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111259746 | ||||||
| chr13:111259873
|
A | T | 2 | a0001c0001t0003g0145a0001c0001t0003g0210 | 2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.951-7675A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111259873 | ||||||
| chr13:111259888
|
T | C | 2 | a0001c0001t0003g0024a0001c0001t0017g0270 | 2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.951-7660T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111259888 | ||||||
| chr13:111259925
|
A | G | 32 | a0001c0002t0001g0170a0001c0002t0001g0182a0001c0002t0002g0031others(29): Show | 32 | HG00558.hp1 HG00597.hp2 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.951-7623A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111259925 | ||||||
| chr13:111259970
|
C | T | 4 | a0001c0001t0029g0201a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18941.hp2 NA18957.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.951-7578C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111259970 | ||||||
| chr13:111260029
|
G | C | 15 | a0001c0001t0001g0048a0001c0001t0001g0092a0001c0001t0001g0097others(12): Show | 15 | HG00140.hp2 HG00642.hp2 HG00741.hp2 others(12): Show |
intron_variant | MODIFIER | c.951-7519G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111260029 | ||||||
| chr13:111260092
|
T | G | 3 | a0001c0001t0016g0012a0001c0001t0016g0077a0001c0012t0030g0072 | 3 | HG02280.hp2 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.951-7456T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111260092 | ||||||
| chr13:111260249
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-7299G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111260249 | ||||||
| chr13:111260276
|
C | T | 2 | a0001c0006t0012g0121a0001c0006t0012g0124 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.951-7272C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111260276 | ||||||
| chr13:111260400
|
G | T | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.951-7148G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111260400 | ||||||
| chr13:111260678
|
C | T | 1 | a0001c0001t0004g0247 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.951-6870C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111260678 | ||||||
| chr13:111260828
|
A | C | 2 | a0001c0001t0007g0010a0001c0001t0023g0036 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.951-6720A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111260828 | ||||||
| chr13:111260907
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-6641A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111260907 | ||||||
| chr13:111261037
|
A | G | 53 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(50): Show | 53 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.951-6511A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111261037 | ||||||
| chr13:111261060
|
A | T | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.951-6488A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111261060 | ||||||
| chr13:111261086
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-6462G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111261086 | ||||||
| chr13:111261212
|
C | A | 2 | a0001c0001t0004g0238a0001c0001t0004g0239 | 2 | HG02135.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.951-6336C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111261212 | ||||||
| chr13:111261283
|
C | T | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.951-6265C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111261283 | ||||||
| chr13:111261295
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-6253A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111261295 | ||||||
| chr13:111261366
|
A | C | 4 | a0001c0001t0029g0201a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18941.hp2 NA18957.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.951-6182A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111261366 | ||||||
| chr13:111261726
|
T | A | 3 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0023g0036 | 3 | HG02109.hp1 HG02258.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.951-5822T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111261726 | ||||||
| chr13:111261827
|
A | G | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.951-5721A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111261827 | ||||||
| chr13:111261898
|
T | A | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.951-5650T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111261898 | ||||||
| chr13:111261904
|
T | C | 15 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(12): Show | 15 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.951-5644T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111261904 | ||||||
| chr13:111261955
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-5593A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111261955 | ||||||
| chr13:111262002
|
A | G | 2 | a0001c0006t0012g0121a0001c0006t0012g0124 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.951-5546A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111262002 | ||||||
| chr13:111262081
|
A | C | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-5467A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111262081 | ||||||
| chr13:111262135
|
T | C | 1 | a0001c0001t0029g0201 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.951-5413T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111262135 | ||||||
| chr13:111262147
|
G | A | 2 | a0001c0007t0004g0059a0001c0007t0027g0054 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.951-5401G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111262147 | ||||||
| chr13:111262212
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-5336A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111262212 | ||||||
| chr13:111262245
|
T | C | 235 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.951-5303T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111262245 | ||||||
| chr13:111262360
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.951-5188C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111262360 | ||||||
| chr13:111262374
|
T | C | 1 | a0001c0001t0003g0085 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.951-5174T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111262374 | ||||||
| chr13:111262398
|
C | CTG | 3 | a0001c0001t0003g0025a0001c0001t0016g0143a0001c0001t0019g0071 | 3 | HG02922.hp2 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.951-5137_951-5136d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111262398 | |||||
| chr13:111262413
|
CAT | C | 3 | a0001c0001t0006g0042a0001c0005t0020g0117a0001c0005t0020g0118 | 3 | HG01243.hp1 HG02300.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.951-5134_951-5133d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111262413 | ||||||
| chr13:111262432
|
A | G | 1 | a0001c0001t0004g0224 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.951-5116A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111262432 | ||||||
| chr13:111262604
|
T | G | 5 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(2): Show | 5 | HG01192.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.951-4944T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111262604 | ||||||
| chr13:111262658
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-4890A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111262658 | ||||||
| chr13:111262664
|
C | T | 2 | a0001c0008t0001g0098a0001c0008t0001g0109 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.951-4884C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111262664 | ||||||
| chr13:111262774
|
C | T | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.951-4774C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111262774 | ||||||
| chr13:111262797
|
G | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-4751G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111262797 | ||||||
| chr13:111262837
|
C | T | 2 | a0001c0001t0015g0271a0001c0001t0015g0273 | 2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.951-4711C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111262837 | ||||||
| chr13:111262924
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-4624A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111262924 | ||||||
| chr13:111262943
|
C | T | 4 | a0001c0001t0029g0201a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18941.hp2 NA18957.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.951-4605C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111262943 | ||||||
| chr13:111263010
|
G | C | 6 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(3): Show | 6 | HG01081.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.951-4538G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111263010 | ||||||
| chr13:111263331
|
G | A | 2 | a0001c0002t0001g0170a0001c0002t0024g0183 | 2 | HG01257.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.951-4217G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111263331 | ||||||
| chr13:111263377
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-4171G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111263377 | ||||||
| chr13:111263402
|
CTTAA | C | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-4143_951-4140d others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111263402 | |||||
| chr13:111263500
|
G | C | 1 | a0001c0001t0001g0229 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.951-4048G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111263500 | ||||||
| chr13:111263515
|
C | T | 1 | a0001c0001t0003g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.951-4033C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111263515 | ||||||
| chr13:111263806
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-3742G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111263806 | ||||||
| chr13:111263812
|
TTCC | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.951-3730_951-3728d others(5): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111263812 | |||||
| chr13:111263840
|
G | T | 2 | a0001c0002t0002g0079a0001c0002t0002g0165 | 2 | HG02015.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.951-3708G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111263840 | ||||||
| chr13:111263884
|
C | T | 235 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.951-3664C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111263884 | ||||||
| chr13:111264036
|
T | TAATCCCG others(12): Show |
1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.951-3509_951-3491d others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111264036 | |||||
| chr13:111264134
|
T | C | 43 | a0001c0001t0001g0084a0001c0001t0002g0029a0001c0001t0002g0156others(40): Show | 43 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.951-3414T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111264134 | ||||||
| chr13:111264147
|
C | T | 2 | a0001c0002t0002g0151a0001c0002t0002g0152 | 2 | NA18941.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.951-3401C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111264147 | ||||||
| chr13:111264350
|
T | A | 14 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(11): Show | 14 | HG01243.hp1 HG02257.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.951-3198T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111264350 | ||||||
| chr13:111264451
|
C | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-3097C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111264451 | ||||||
| chr13:111264479
|
C | A | 1 | a0001c0001t0009g0202 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.951-3069C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111264479 | ||||||
| chr13:111264608
|
G | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-2940G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111264608 | ||||||
| chr13:111264647
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-2901G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111264647 | ||||||
| chr13:111264679
|
G | A | 52 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(49): Show | 52 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.951-2869G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111264679 | ||||||
| chr13:111264775
|
C | T | 2 | a0001c0001t0008g0035a0001c0016t0008g0227 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.951-2773C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111264775 | ||||||
| chr13:111264795
|
G | A | 1 | a0001c0001t0029g0201 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.951-2753G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111264795 | ||||||
| chr13:111264980
|
T | C | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-2568T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111264980 | ||||||
| chr13:111264982
|
G | T | 4 | a0001c0001t0029g0201a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18941.hp2 NA18957.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.951-2566G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111264982 | ||||||
| chr13:111265017
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017 | 3 | HG01109.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.951-2531G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111265017 | ||||||
| chr13:111265095
|
G | A | 1 | a0006c0019t0002g0175 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.951-2453G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111265095 | ||||||
| chr13:111265097
|
C | A | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.951-2451C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111265097 | ||||||
| chr13:111265124
|
C | CA | 52 | a0001c0001t0001g0039a0001c0001t0001g0096a0001c0001t0003g0085others(49): Show | 52 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.951-2401dupA | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111265124 | |||||
| chr13:111265124
|
C | CAA | 22 | a0001c0001t0001g0084a0001c0001t0002g0011a0001c0001t0002g0029others(19): Show | 22 | HG00140.hp1 HG01099.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.951-2402_951-2401d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111265124 | |||||
| chr13:111265124
|
CA | C | 63 | a0001c0001t0001g0018a0001c0001t0001g0043a0001c0001t0001g0052others(60): Show | 63 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.951-2401delA | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111265124 | |||||
| chr13:111265249
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.951-2299C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111265249 | ||||||
| chr13:111265256
|
G | A | 5 | a0001c0001t0001g0040a0001c0001t0001g0231a0001c0001t0001g0232others(2): Show | 5 | NA18952.hp2 NA18957.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.951-2292G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111265256 | ||||||
| chr13:111265268
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.951-2280C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111265268 | ||||||
| chr13:111265291
|
T | G | 20 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(17): Show | 20 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.951-2257T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111265291 | ||||||
| chr13:111265690
|
C | G | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.951-1858C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111265690 | ||||||
| chr13:111265946
|
A | T | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.951-1602A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111265946 | ||||||
| chr13:111265965
|
G | A | 1 | a0001c0001t0001g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.951-1583G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111265965 | ||||||
| chr13:111266024
|
G | A | 4 | a0001c0001t0029g0201a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18941.hp2 NA18957.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.951-1524G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111266024 | ||||||
| chr13:111266116
|
C | T | 1 | a0001c0001t0007g0008 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.951-1432C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111266116 | ||||||
| chr13:111266206
|
C | G | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.951-1342C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111266206 | ||||||
| chr13:111266349
|
T | C | 1 | a0001c0001t0003g0107 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.951-1199T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111266349 | ||||||
| chr13:111266381
|
C | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-1167C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111266381 | ||||||
| chr13:111266399
|
C | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-1149C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111266399 | ||||||
| chr13:111266429
|
C | T | 1 | a0001c0002t0010g0080 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.951-1119C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111266429 | ||||||
| chr13:111266569
|
T | TGTC | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-978_951-976dup others(3): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111266569 | |||||
| chr13:111266664
|
T | C | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-884T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111266664 | ||||||
| chr13:111266872
|
T | C | 1 | a0001c0005t0020g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.951-676T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111266872 | ||||||
| chr13:111266917
|
A | G | 2 | a0001c0001t0003g0024a0001c0001t0017g0270 | 2 | HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.951-631A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111266917 | ||||||
| chr13:111267061
|
T | G | 4 | a0001c0001t0003g0119a0001c0001t0018g0020a0001c0001t0018g0038others(1): Show | 4 | HG00738.hp1 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.951-487T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111267061 | ||||||
| chr13:111267078
|
T | C | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.951-470T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111267078 | ||||||
| chr13:111267109
|
G | A | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.951-439G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111267109 | ||||||
| chr13:111267195
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.951-353C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111267195 | ||||||
| chr13:111267230
|
T | C | 4 | a0001c0002t0002g0147a0001c0002t0002g0148a0001c0002t0002g0149others(1): Show | 4 | HG01175.hp1 HG01361.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.951-318T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111267230 | ||||||
| chr13:111267305
|
TTGGGATG others(165): Show |
T | 1 | a0001c0002t0002g0060 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.951-240_951-69del | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | 111267305 | |||||
| chr13:111267346
|
G | A | 2 | a0001c0001t0006g0032a0001c0001t0006g0083 | 2 | HG00558.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.951-202G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111267346 | ||||||
| chr13:111267403
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.951-145A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111267403 | ||||||
| chr13:111267470
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(4): Show | 7 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.951-78G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111267470 | ||||||
| chr13:111267535
|
C | T | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.951-13C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | chr13 | 111267535 | ||||||
| chr13:111267674
|
C | T | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | splice_region_variant&intron_variant | LOW | c.1073+4C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111267674 | ||||||
| chr13:111267841
|
T | C | 2 | a0001c0006t0012g0121a0001c0006t0012g0124 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1073+171T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111267841 | ||||||
| chr13:111267924
|
TAGTA | T | 39 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(36): Show | 39 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.1073+258_1073+261d others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr13 | 111267924 | |||||
| chr13:111268126
|
C | G | 21 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(18): Show | 21 | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.1073+456C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111268126 | ||||||
| chr13:111268187
|
T | G | 1 | a0001c0001t0004g0254 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1073+517T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111268187 | ||||||
| chr13:111268208
|
C | G | 2 | a0001c0002t0002g0155a0001c0002t0002g0221 | 2 | HG00597.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1073+538C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111268208 | ||||||
| chr13:111268246
|
G | C | 2 | a0001c0001t0005g0102a0001c0001t0005g0103 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1073+576G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111268246 | ||||||
| chr13:111268253
|
G | T | 1 | a0001c0001t0002g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1073+583G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111268253 | ||||||
| chr13:111268361
|
A | G | 3 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017 | 3 | HG01109.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1073+691A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111268361 | ||||||
| chr13:111268398
|
T | A | 3 | a0001c0001t0003g0128a0001c0001t0005g0102a0001c0001t0005g0103 | 3 | HG01167.hp1 HG01169.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.1073+728T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111268398 | ||||||
| chr13:111268645
|
G | A | 1 | a0001c0002t0002g0148 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1073+975G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111268645 | ||||||
| chr13:111268733
|
C | A | 4 | a0001c0001t0029g0201a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18941.hp2 NA18957.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1073+1063C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111268733 | ||||||
| chr13:111268795
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0096 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1073+1125G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111268795 | ||||||
| chr13:111268860
|
A | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073+1190A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111268860 | ||||||
| chr13:111268911
|
T | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(65): Show | 68 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.1073+1241T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111268911 | ||||||
| chr13:111269016
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073+1346A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111269016 | ||||||
| chr13:111269319
|
A | AT | 18 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(15): Show | 18 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1073+1650dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr13 | 111269319 | |||||
| chr13:111269331
|
A | C | 2 | a0001c0001t0003g0104a0001c0001t0003g0108 | 2 | HG00099.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1073+1661A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111269331 | ||||||
| chr13:111269396
|
G | T | 4 | a0001c0001t0029g0201a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18941.hp2 NA18957.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1073+1726G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111269396 | ||||||
| chr13:111269413
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1073+1743G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111269413 | ||||||
| chr13:111269626
|
G | A | 49 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0015g0272others(46): Show | 49 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.1073+1956G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111269626 | ||||||
| chr13:111269749
|
C | T | 1 | a0001c0002t0002g0206 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1073+2079C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111269749 | ||||||
| chr13:111269868
|
C | G | 1 | a0001c0002t0002g0204 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1073+2198C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111269868 | ||||||
| chr13:111270145
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073+2475A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111270145 | ||||||
| chr13:111270298
|
C | T | 2 | a0001c0001t0001g0049a0001c0001t0001g0220 | 2 | HG00639.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1073+2628C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111270298 | ||||||
| chr13:111270343
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1073+2673G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111270343 | ||||||
| chr13:111270452
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1073+2782C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111270452 | ||||||
| chr13:111270481
|
A | G | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1073+2811A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111270481 | ||||||
| chr13:111270599
|
G | C | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1073+2929G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111270599 | ||||||
| chr13:111270644
|
G | A | 3 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017 | 3 | HG01109.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1073+2974G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111270644 | ||||||
| chr13:111270710
|
T | A | 1 | a0001c0001t0018g0038 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1073+3040T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111270710 | ||||||
| chr13:111270959
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1074-2855G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111270959 | ||||||
| chr13:111271003
|
T | C | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074-2811T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111271003 | ||||||
| chr13:111271030
|
G | T | 273 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1074-2784G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111271030 | ||||||
| chr13:111271056
|
CGGCAGTG others(8): Show |
C | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1074-2750_1074-273 others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr13 | 111271056 | |||||
| chr13:111271076
|
G | A | 1 | a0001c0001t0003g0184 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1074-2738G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111271076 | ||||||
| chr13:111271185
|
A | G | 1 | a0001c0001t0012g0001 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1074-2629A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111271185 | ||||||
| chr13:111271439
|
A | G | 1 | a0001c0001t0004g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1074-2375A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111271439 | ||||||
| chr13:111271640
|
G | A | 2 | a0001c0001t0007g0010a0001c0001t0023g0036 | 2 | HG02109.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1074-2174G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111271640 | ||||||
| chr13:111271799
|
T | G | 2 | a0001c0001t0004g0133a0001c0001t0004g0134 | 2 | NA19066.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1074-2015T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111271799 | ||||||
| chr13:111271921
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1074-1893G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111271921 | ||||||
| chr13:111272048
|
G | T | 2 | a0001c0007t0004g0059a0001c0007t0027g0054 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1074-1766G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111272048 | ||||||
| chr13:111272320
|
G | A | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1074-1494G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111272320 | ||||||
| chr13:111272491
|
T | C | 1 | a0001c0001t0004g0242 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1074-1323T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111272491 | ||||||
| chr13:111272611
|
A | G | 1 | a0001c0002t0002g0190 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1074-1203A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111272611 | ||||||
| chr13:111272613
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1074-1201C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111272613 | ||||||
| chr13:111272663
|
A | T | 1 | a0005c0018t0013g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1074-1151A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111272663 | ||||||
| chr13:111272716
|
A | G | 1 | a0006c0019t0002g0175 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1074-1098A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111272716 | ||||||
| chr13:111272830
|
A | G | 2 | a0001c0006t0012g0121a0001c0006t0012g0124 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1074-984A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111272830 | ||||||
| chr13:111272851
|
C | T | 103 | a0001c0001t0001g0084a0001c0001t0001g0144a0001c0001t0002g0011others(100): Show | 103 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1074-963C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111272851 | ||||||
| chr13:111272853
|
G | A | 2 | a0001c0008t0001g0098a0001c0008t0001g0109 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1074-961G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111272853 | ||||||
| chr13:111272999
|
G | A | 2 | a0001c0006t0012g0121a0001c0006t0012g0124 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1074-815G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111272999 | ||||||
| chr13:111273037
|
T | C | 21 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(18): Show | 21 | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.1074-777T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111273037 | ||||||
| chr13:111273040
|
T | C | 109 | a0001c0001t0001g0019a0001c0001t0001g0084a0001c0001t0001g0129others(106): Show | 109 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.1074-774T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111273040 | ||||||
| chr13:111273077
|
A | G | 4 | a0001c0001t0001g0084a0001c0001t0001g0144a0001c0001t0002g0011others(1): Show | 4 | HG01109.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074-737A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111273077 | ||||||
| chr13:111273086
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1074-728A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111273086 | ||||||
| chr13:111273118
|
C | T | 3 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233 | 3 | NA18957.hp2 NA19065.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1074-696C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111273118 | ||||||
| chr13:111273264
|
G | A | 1 | a0001c0001t0012g0001 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1074-550G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111273264 | ||||||
| chr13:111273359
|
C | T | 2 | a0001c0001t0007g0028a0001c0001t0007g0132 | 2 | HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1074-455C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111273359 | ||||||
| chr13:111273363
|
C | G | 2 | a0001c0007t0004g0059a0001c0007t0027g0054 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1074-451C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111273363 | ||||||
| chr13:111273393
|
C | T | 1 | a0001c0001t0016g0077 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1074-421C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111273393 | ||||||
| chr13:111273418
|
G | A | 2 | a0001c0002t0002g0082a0001c0002t0002g0157 | 2 | NA18979.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1074-396G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111273418 | ||||||
| chr13:111273436
|
T | G | 11 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1074-378T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111273436 | ||||||
| chr13:111273540
|
G | A | 3 | a0001c0001t0002g0091a0001c0001t0015g0271a0001c0001t0015g0273 | 3 | HG03453.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1074-274G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111273540 | ||||||
| chr13:111273653
|
C | T | 1 | a0001c0001t0006g0185 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1074-161C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111273653 | ||||||
| chr13:111273721
|
T | A | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1074-93T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111273721 | ||||||
| chr13:111273744
|
T | C | 4 | a0001c0001t0029g0201a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18941.hp2 NA18957.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074-70T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111273744 | ||||||
| chr13:111273773
|
A | G | 1 | a0001c0001t0006g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1074-41A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 9/21 | chr13 | 111273773 | ||||||
| chr13:111274360
|
ACT | A | 4 | a0001c0001t0006g0032a0001c0001t0006g0083a0001c0001t0006g0218others(1): Show | 4 | HG00558.hp2 NA18939.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.1213-366_1213-365d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr13 | 111274360 | |||||
| chr13:111274447
|
A | T | 66 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(63): Show | 66 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.1213-284A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 10/21 | chr13 | 111274447 | ||||||
| chr13:111274573
|
C | T | 1 | a0001c0001t0004g0045 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1213-158C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 10/21 | chr13 | 111274573 | ||||||
| chr13:111274697
|
A | G | 4 | a0001c0001t0007g0008a0001c0001t0007g0010a0001c0001t0023g0036others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1213-34A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 10/21 | chr13 | 111274697 | ||||||
| chr13:111274698
|
T | A | 21 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(18): Show | 21 | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.1213-33T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 10/21 | chr13 | 111274698 | ||||||
| chr13:111274814
|
T | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0066a0001c0001t0001g0074others(1): Show | 4 | HG01192.hp1 HG02647.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1272+24T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 11/21 | chr13 | 111274814 | ||||||
| chr13:111275070
|
T | C | 3 | a0001c0001t0001g0050a0001c0001t0001g0172a0001c0001t0028g0127 | 3 | HG01192.hp2 HG01496.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1272+280T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 11/21 | chr13 | 111275070 | ||||||
| chr13:111275130
|
G | A | 1 | a0001c0001t0003g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1272+340G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 11/21 | chr13 | 111275130 | ||||||
| chr13:111275193
|
C | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1273-339C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 11/21 | chr13 | 111275193 | ||||||
| chr13:111275258
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1273-274T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 11/21 | chr13 | 111275258 | ||||||
| chr13:111275355
|
A | G | 2 | a0001c0001t0001g0092a0001c0001t0001g0177 | 2 | HG01099.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1273-177A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 11/21 | chr13 | 111275355 | ||||||
| chr13:111275414
|
G | A | 1 | a0001c0001t0005g0230 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1273-118G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 11/21 | chr13 | 111275414 | ||||||
| chr13:111275424
|
G | A | 5 | a0001c0001t0005g0139a0001c0001t0005g0140a0001c0001t0005g0141others(2): Show | 5 | HG01257.hp2 HG01361.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273-108G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 11/21 | chr13 | 111275424 | ||||||
| chr13:111275926
|
A | G | 2 | a0001c0001t0001g0097a0001c0001t0032g0030 | 2 | HG00140.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1419+248A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111275926 | ||||||
| chr13:111275983
|
T | C | 8 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(5): Show | 8 | HG01192.hp1 HG02809.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1419+305T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111275983 | ||||||
| chr13:111276177
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0032g0030 | 2 | HG00140.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1419+499C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111276177 | ||||||
| chr13:111276260
|
C | T | 273 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1419+582C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111276260 | ||||||
| chr13:111276355
|
A | C | 4 | a0001c0001t0029g0201a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18941.hp2 NA18957.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1419+677A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111276355 | ||||||
| chr13:111276365
|
C | T | 6 | a0001c0001t0007g0004a0001c0001t0007g0009a0001c0001t0007g0028others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1419+687C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111276365 | ||||||
| chr13:111276369
|
T | C | 1 | a0001c0001t0005g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1419+691T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111276369 | ||||||
| chr13:111276390
|
C | T | 2 | a0001c0001t0003g0104a0001c0001t0003g0108 | 2 | HG00099.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.1419+712C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111276390 | ||||||
| chr13:111276620
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1419+942G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111276620 | ||||||
| chr13:111276683
|
A | G | 1 | a0003c0011t0005g0191 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1420-904A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111276683 | ||||||
| chr13:111276724
|
T | A | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1420-863T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111276724 | ||||||
| chr13:111276734
|
C | T | 1 | a0001c0002t0001g0182 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1420-853C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111276734 | ||||||
| chr13:111276801
|
A | G | 5 | a0001c0001t0004g0222a0001c0001t0004g0223a0001c0001t0004g0224others(2): Show | 5 | HG01261.hp2 HG02109.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.1420-786A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111276801 | ||||||
| chr13:111276823
|
G | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1420-764G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111276823 | ||||||
| chr13:111276889
|
T | G | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1420-698T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111276889 | ||||||
| chr13:111276976
|
A | G | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1420-611A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111276976 | ||||||
| chr13:111277067
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1420-520G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111277067 | ||||||
| chr13:111277110
|
A | G | 4 | a0001c0001t0001g0084a0001c0001t0001g0144a0001c0001t0002g0011others(1): Show | 4 | HG01109.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1420-477A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111277110 | ||||||
| chr13:111277134
|
C | T | 3 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0008g0017 | 3 | HG01109.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1420-453C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111277134 | ||||||
| chr13:111277149
|
A | G | 2 | a0001c0006t0012g0121a0001c0006t0012g0124 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1420-438A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111277149 | ||||||
| chr13:111277151
|
C | T | 1 | a0001c0002t0002g0149 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1420-436C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111277151 | ||||||
| chr13:111277252
|
A | C | 4 | a0001c0001t0001g0084a0001c0001t0001g0144a0001c0001t0002g0011others(1): Show | 4 | HG01109.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1420-335A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111277252 | ||||||
| chr13:111277253
|
A | G | 1 | a0001c0001t0004g0254 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1420-334A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111277253 | ||||||
| chr13:111277268
|
G | A | 21 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(18): Show | 21 | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.1420-319G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111277268 | ||||||
| chr13:111277301
|
T | C | 1 | a0001c0005t0020g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1420-286T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111277301 | ||||||
| chr13:111277307
|
G | C | 2 | a0001c0001t0015g0271a0001c0001t0015g0273 | 2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1420-280G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 12/21 | chr13 | 111277307 | ||||||
| chr13:111277885
|
A | T | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1506+212A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/21 | chr13 | 111277885 | ||||||
| chr13:111278107
|
T | C | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1506+434T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/21 | chr13 | 111278107 | ||||||
| chr13:111278221
|
C | T | 1 | a0001c0001t0003g0213 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1506+548C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/21 | chr13 | 111278221 | ||||||
| chr13:111278405
|
C | T | 1 | a0001c0001t0003g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1506+732C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/21 | chr13 | 111278405 | ||||||
| chr13:111278414
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1506+741C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/21 | chr13 | 111278414 | ||||||
| chr13:111278520
|
C | T | 1 | a0001c0002t0001g0182 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1506+847C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/21 | chr13 | 111278520 | ||||||
| chr13:111278614
|
G | A | 273 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1506+941G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/21 | chr13 | 111278614 | ||||||
| chr13:111278787
|
T | C | 2 | a0001c0007t0004g0059a0001c0007t0027g0054 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1506+1114T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/21 | chr13 | 111278787 | ||||||
| chr13:111278818
|
C | T | 1 | a0001c0002t0002g0174 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1506+1145C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/21 | chr13 | 111278818 | ||||||
| chr13:111278920
|
T | A | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1506+1247T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/21 | chr13 | 111278920 | ||||||
| chr13:111279054
|
C | T | 2 | a0001c0001t0002g0099a0001c0015t0002g0023 | 2 | HG03130.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1507-1218C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/21 | chr13 | 111279054 | ||||||
| chr13:111279211
|
A | G | 2 | a0001c0001t0016g0143a0001c0001t0019g0071 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1507-1061A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/21 | chr13 | 111279211 | ||||||
| chr13:111279329
|
G | A | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1507-943G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/21 | chr13 | 111279329 | ||||||
| chr13:111279332
|
G | T | 1 | a0001c0001t0006g0041 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1507-940G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/21 | chr13 | 111279332 | ||||||
| chr13:111279629
|
C | G | 1 | a0001c0001t0001g0217 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1507-643C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/21 | chr13 | 111279629 | ||||||
| chr13:111279871
|
T | G | 1 | a0001c0001t0003g0240 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1507-401T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/21 | chr13 | 111279871 | ||||||
| chr13:111279964
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1507-308A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/21 | chr13 | 111279964 | ||||||
| chr13:111280145
|
T | G | 1 | a0001c0001t0003g0228 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1507-127T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 13/21 | chr13 | 111280145 | ||||||
| chr13:111280746
|
G | A | 1 | a0001c0001t0007g0010 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1725+69G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111280746 | ||||||
| chr13:111280751
|
C | G | 103 | a0001c0001t0001g0084a0001c0001t0001g0129a0001c0001t0001g0137others(100): Show | 103 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.1725+74C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111280751 | ||||||
| chr13:111280753
|
G | A | 2 | a0001c0006t0012g0121a0001c0006t0012g0124 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1725+76G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111280753 | ||||||
| chr13:111280900
|
C | T | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1725+223C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111280900 | ||||||
| chr13:111280943
|
G | A | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1725+266G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111280943 | ||||||
| chr13:111280964
|
T | G | 5 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(2): Show | 5 | HG01192.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1725+287T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111280964 | ||||||
| chr13:111281010
|
T | A | 1 | a0001c0001t0009g0214 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1725+333T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111281010 | ||||||
| chr13:111281157
|
A | G | 2 | a0001c0006t0012g0121a0001c0006t0012g0124 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1725+480A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111281157 | ||||||
| chr13:111281181
|
C | CT | 63 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(60): Show | 63 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.1725+532dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | 111281181 | |||||
| chr13:111281181
|
C | CTT | 28 | a0001c0001t0001g0039a0001c0001t0001g0047a0001c0001t0001g0052others(25): Show | 28 | HG00280.hp1 HG00558.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.1725+531_1725+532d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | 111281181 | |||||
| chr13:111281181
|
C | CTTT | 7 | a0001c0001t0001g0019a0001c0001t0001g0066a0001c0001t0001g0131others(4): Show | 7 | HG00741.hp1 HG01081.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1725+530_1725+532d others(5): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | 111281181 | |||||
| chr13:111281181
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0084a0001c0001t0005g0141 | 2 | HG01257.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1725+522_1725+532d others(13): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | 111281181 | |||||
| chr13:111281181
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0005g0139a0001c0001t0005g0230 | 2 | HG01071.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1725+521_1725+532d others(14): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | 111281181 | |||||
| chr13:111281181
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0003g0128a0001c0001t0005g0115a0001c0001t0005g0140 | 3 | HG01361.hp1 HG01952.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1725+520_1725+532d others(15): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | 111281181 | |||||
| chr13:111281181
|
C | CTTTTTTT others(11): Show |
1 | a0003c0011t0005g0191 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1725+515_1725+532d others(20): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | 111281181 | |||||
| chr13:111281181
|
C | CTTTTTTT others(12): Show |
2 | a0001c0001t0005g0102a0001c0001t0005g0103 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1725+514_1725+532d others(21): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | 111281181 | |||||
| chr13:111281181
|
CT | C | 43 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0002g0156others(40): Show | 43 | HG00099.hp2 HG00323.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.1725+532delT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | 111281181 | |||||
| chr13:111281181
|
CTT | C | 52 | a0001c0001t0003g0024a0001c0001t0003g0178a0001c0001t0003g0216others(49): Show | 52 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.1725+531_1725+532d others(4): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | 111281181 | |||||
| chr13:111281181
|
CTTTT | C | 10 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0007g0094others(7): Show | 10 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1725+529_1725+532d others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | 111281181 | |||||
| chr13:111281181
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0003g0025a0001c0001t0004g0122 | 2 | HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1725+519_1725+532d others(16): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | 111281181 | |||||
| chr13:111281181
|
CTTTTTTT others(10): Show |
C | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1725+516_1725+532d others(19): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | 111281181 | |||||
| chr13:111281209
|
T | A | 3 | a0001c0001t0003g0107a0002c0009t0002g0069a0002c0009t0002g0112 | 3 | HG02572.hp1 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1725+532T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111281209 | ||||||
| chr13:111281294
|
T | G | 2 | a0001c0001t0003g0245a0001c0001t0003g0249 | 2 | NA19060.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.1725+617T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111281294 | ||||||
| chr13:111281412
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0074 | 2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1725+735G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111281412 | ||||||
| chr13:111281651
|
C | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1725+974C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111281651 | ||||||
| chr13:111281736
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1725+1059A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111281736 | ||||||
| chr13:111281825
|
C | T | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1725+1148C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111281825 | ||||||
| chr13:111281826
|
G | A | 1 | a0001c0015t0002g0023 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1725+1149G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111281826 | ||||||
| chr13:111282006
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1726-1133C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111282006 | ||||||
| chr13:111282193
|
T | TGCTGTGT others(1): Show |
273 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1726-944_1726-943i others(10): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | 111282193 | |||||
| chr13:111282234
|
C | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1726-905C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111282234 | ||||||
| chr13:111282249
|
C | T | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1726-890C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111282249 | ||||||
| chr13:111282277
|
A | G | 235 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.1726-862A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111282277 | ||||||
| chr13:111282290
|
C | G | 1 | a0001c0002t0002g0194 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1726-849C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111282290 | ||||||
| chr13:111282476
|
TA | T | 53 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0003g0024others(50): Show | 53 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.1726-660delA | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr13 | 111282476 | |||||
| chr13:111282541
|
T | G | 224 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(221): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.1726-598T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111282541 | ||||||
| chr13:111282594
|
T | C | 3 | a0001c0001t0007g0010a0001c0001t0023g0036a0001c0001t0023g0037 | 3 | HG02109.hp1 HG02258.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1726-545T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111282594 | ||||||
| chr13:111282730
|
C | T | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1726-409C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111282730 | ||||||
| chr13:111282741
|
G | C | 1 | a0001c0002t0002g0198 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1726-398G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111282741 | ||||||
| chr13:111282793
|
C | G | 1 | a0001c0002t0002g0237 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1726-346C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111282793 | ||||||
| chr13:111282920
|
C | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1726-219C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111282920 | ||||||
| chr13:111283001
|
A | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1726-138A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111283001 | ||||||
| chr13:111283058
|
G | A | 1 | a0001c0001t0004g0086 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1726-81G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111283058 | ||||||
| chr13:111283065
|
C | T | 1 | a0001c0002t0002g0199 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1726-74C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111283065 | ||||||
| chr13:111283066
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1726-73G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 15/21 | chr13 | 111283066 | ||||||
| chr13:111283907
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1950+544G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111283907 | ||||||
| chr13:111283964
|
T | C | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1950+601T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111283964 | ||||||
| chr13:111284153
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(4): Show | 7 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1950+790G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111284153 | ||||||
| chr13:111284154
|
C | T | 3 | a0001c0002t0010g0081a0001c0002t0010g0159a0001c0002t0010g0197 | 3 | NA18968.hp2 NA18999.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1950+791C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111284154 | ||||||
| chr13:111284288
|
A | G | 2 | a0001c0001t0015g0271a0001c0001t0015g0273 | 2 | HG03453.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1950+925A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111284288 | ||||||
| chr13:111284296
|
G | C | 1 | a0001c0001t0004g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1950+933G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111284296 | ||||||
| chr13:111284325
|
C | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1950+962C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111284325 | ||||||
| chr13:111284440
|
A | G | 7 | a0001c0001t0002g0099a0001c0001t0004g0122a0001c0003t0001g0142others(4): Show | 7 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1950+1077A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111284440 | ||||||
| chr13:111284506
|
G | A | 1 | a0001c0001t0012g0001 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1950+1143G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111284506 | ||||||
| chr13:111284540
|
T | G | 1 | a0001c0001t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1950+1177T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111284540 | ||||||
| chr13:111284669
|
C | T | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1950+1306C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111284669 | ||||||
| chr13:111284821
|
G | GGC | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1951-1326_1951-132 others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111284821 | ||||||
| chr13:111284822
|
C | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1951-1325C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111284822 | ||||||
| chr13:111285136
|
T | C | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1951-1011T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111285136 | ||||||
| chr13:111285207
|
TTCCATGG others(5): Show |
T | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1951-933_1951-922d others(14): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr13 | 111285207 | |||||
| chr13:111285305
|
C | T | 87 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(84): Show | 87 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.1951-842C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111285305 | ||||||
| chr13:111285371
|
T | A | 2 | a0001c0007t0004g0059a0001c0007t0027g0054 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1951-776T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111285371 | ||||||
| chr13:111285438
|
T | A | 1 | a0001c0001t0002g0156 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1951-709T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111285438 | ||||||
| chr13:111285461
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1951-686G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111285461 | ||||||
| chr13:111285550
|
G | A | 1 | a0001c0001t0001g0135 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1951-597G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111285550 | ||||||
| chr13:111285844
|
C | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1951-303C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111285844 | ||||||
| chr13:111285938
|
C | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1951-209C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111285938 | ||||||
| chr13:111285960
|
C | T | 3 | a0001c0001t0016g0012a0001c0001t0016g0077a0001c0012t0030g0072 | 3 | HG02280.hp2 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1951-187C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111285960 | ||||||
| chr13:111286136
|
T | A | 21 | a0001c0001t0006g0032a0001c0001t0006g0041a0001c0001t0006g0042others(18): Show | 21 | HG00558.hp2 HG00642.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.1951-11T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 16/21 | chr13 | 111286136 | ||||||
| chr13:111286370
|
G | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0219 | 2 | HG00099.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2044+130G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111286370 | ||||||
| chr13:111286542
|
C | T | 214 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(211): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.2044+302C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111286542 | ||||||
| chr13:111286590
|
A | G | 4 | a0001c0001t0029g0201a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18941.hp2 NA18957.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.2044+350A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111286590 | ||||||
| chr13:111286633
|
C | G | 234 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2044+393C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111286633 | ||||||
| chr13:111286739
|
T | C | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2044+499T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111286739 | ||||||
| chr13:111286947
|
G | A | 1 | a0001c0001t0003g0252 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2044+707G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111286947 | ||||||
| chr13:111286993
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2044+753G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111286993 | ||||||
| chr13:111287080
|
C | G | 1 | a0001c0001t0007g0008 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2044+840C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111287080 | ||||||
| chr13:111287111
|
T | A | 2 | a0001c0006t0012g0121a0001c0006t0012g0124 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.2044+871T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111287111 | ||||||
| chr13:111287111
|
T | C | 5 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0003g0025others(2): Show | 5 | HG01109.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2044+871T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111287111 | ||||||
| chr13:111287231
|
G | A | 2 | a0001c0001t0003g0119a0001c0001t0033g0101 | 2 | HG00738.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2044+991G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111287231 | ||||||
| chr13:111287391
|
G | A | 5 | a0001c0001t0001g0144a0001c0001t0002g0011a0001c0001t0003g0025others(2): Show | 5 | HG01109.hp1 HG02886.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2045-963G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111287391 | ||||||
| chr13:111287419
|
C | T | 1 | a0001c0001t0002g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2045-935C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111287419 | ||||||
| chr13:111287451
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2045-903G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111287451 | ||||||
| chr13:111287488
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2045-866G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111287488 | ||||||
| chr13:111287611
|
G | A | 2 | a0001c0002t0001g0170a0001c0002t0024g0183 | 2 | HG01257.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.2045-743G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111287611 | ||||||
| chr13:111287643
|
G | A | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2045-711G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111287643 | ||||||
| chr13:111287695
|
T | C | 1 | a0001c0001t0006g0218 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2045-659T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111287695 | ||||||
| chr13:111287703
|
A | AC | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2045-648dupC | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr13 | 111287703 | |||||
| chr13:111287721
|
A | T | 2 | a0001c0001t0004g0133a0001c0001t0004g0134 | 2 | NA19066.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2045-633A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111287721 | ||||||
| chr13:111287757
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2045-597A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111287757 | ||||||
| chr13:111287816
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2045-538C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111287816 | ||||||
| chr13:111287906
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2045-448A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111287906 | ||||||
| chr13:111287962
|
G | C | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2045-392G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111287962 | ||||||
| chr13:111287980
|
T | C | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2045-374T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111287980 | ||||||
| chr13:111288141
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2045-213A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111288141 | ||||||
| chr13:111288291
|
G | A | 1 | a0001c0001t0002g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2045-63G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 17/21 | chr13 | 111288291 | ||||||
| chr13:111288513
|
G | A | 1 | a0001c0001t0001g0048 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2134+70G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111288513 | ||||||
| chr13:111288557
|
T | G | 2 | a0001c0001t0012g0001a0007c0010t0001g0095 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2134+114T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111288557 | ||||||
| chr13:111288611
|
C | T | 4 | a0001c0001t0029g0201a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18941.hp2 NA18957.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.2134+168C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111288611 | ||||||
| chr13:111288665
|
A | AT | 65 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.2134+226dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr13 | 111288665 | |||||
| chr13:111288722
|
A | G | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2134+279A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111288722 | ||||||
| chr13:111288757
|
A | G | 4 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2134+314A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111288757 | ||||||
| chr13:111288923
|
A | T | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.2134+480A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111288923 | ||||||
| chr13:111288997
|
T | C | 11 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0096others(8): Show | 11 | HG01884.hp1 HG01891.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2134+554T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111288997 | ||||||
| chr13:111289038
|
T | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2134+595T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111289038 | ||||||
| chr13:111289259
|
C | G | 40 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0085others(37): Show | 40 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.2134+816C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111289259 | ||||||
| chr13:111289265
|
C | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2134+822C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111289265 | ||||||
| chr13:111289696
|
A | AGGTGCAG others(34): Show |
1 | a0001c0002t0002g0206 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2134+1253_2134+125 others(45): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111289696 | ||||||
| chr13:111289732
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2134+1289G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111289732 | ||||||
| chr13:111289771
|
G | A | 1 | a0001c0005t0020g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2134+1328G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111289771 | ||||||
| chr13:111289795
|
C | CT | 173 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(170): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.2134+1361dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr13 | 111289795 | |||||
| chr13:111289831
|
C | T | 13 | a0001c0001t0003g0128a0001c0001t0005g0063a0001c0001t0005g0102others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.2134+1388C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111289831 | ||||||
| chr13:111289904
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2134+1461T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111289904 | ||||||
| chr13:111290034
|
A | G | 1 | a0001c0001t0005g0115 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2134+1591A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111290034 | ||||||
| chr13:111290343
|
ATTATAC | A | 2 | a0001c0006t0012g0121a0001c0006t0012g0124 | 2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.2135-1769_2135-176 others(10): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr13 | 111290343 | |||||
| chr13:111290529
|
G | A | 2 | a0001c0002t0002g0151a0001c0002t0002g0152 | 2 | NA18941.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.2135-1589G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111290529 | ||||||
| chr13:111290681
|
T | G | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2135-1437T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111290681 | ||||||
| chr13:111290692
|
C | T | 234 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(231): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.2135-1426C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111290692 | ||||||
| chr13:111290725
|
C | T | 3 | a0001c0001t0009g0171a0001c0001t0009g0214a0001c0001t0009g0250 | 3 | NA18982.hp1 NA19076.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.2135-1393C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111290725 | ||||||
| chr13:111290732
|
T | C | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2135-1386T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111290732 | ||||||
| chr13:111291032
|
C | T | 3 | a0001c0001t0016g0012a0001c0001t0016g0077a0001c0012t0030g0072 | 3 | HG02280.hp2 HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2135-1086C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111291032 | ||||||
| chr13:111291067
|
C | T | 1 | a0001c0002t0002g0158 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2135-1051C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111291067 | ||||||
| chr13:111291213
|
C | A | 4 | a0001c0001t0029g0201a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18941.hp2 NA18957.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.2135-905C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111291213 | ||||||
| chr13:111291276
|
C | A | 1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2135-842C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111291276 | ||||||
| chr13:111291442
|
G | A | 3 | a0001c0001t0001g0129a0001c0001t0001g0137a0001c0001t0015g0272 | 3 | HG02145.hp2 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2135-676G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111291442 | ||||||
| chr13:111291472
|
G | A | 1 | a0001c0002t0002g0157 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2135-646G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111291472 | ||||||
| chr13:111291585
|
G | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.2135-533G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111291585 | ||||||
| chr13:111291631
|
T | C | 1 | a0001c0001t0019g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2135-487T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111291631 | ||||||
| chr13:111292063
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2135-55G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111292063 | ||||||
| chr13:111292088
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0012g0013 | 2 | HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2135-30C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 18/21 | chr13 | 111292088 | ||||||
| chr13:111292519
|
A | G | 207 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(204): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.2311+225A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111292519 | ||||||
| chr13:111292557
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0008g0017 | 2 | HG01109.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2311+263G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111292557 | ||||||
| chr13:111293084
|
A | T | 1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2311+790A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111293084 | ||||||
| chr13:111293436
|
TA | T | 223 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(220): Show | 223 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(220): Show |
intron_variant | MODIFIER | c.2311+1160delA | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr13 | 111293436 | |||||
| chr13:111293436
|
TAA | T | 7 | a0001c0001t0002g0099a0001c0001t0005g0103a0001c0001t0006g0083others(4): Show | 7 | HG00558.hp1 HG01169.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.2311+1159_2311+116 others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr13 | 111293436 | |||||
| chr13:111293450
|
A | C | 5 | a0001c0003t0001g0142a0001c0003t0003g0021a0001c0003t0003g0146others(2): Show | 5 | HG01192.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2311+1156A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111293450 | ||||||
| chr13:111293800
|
C | T | 2 | a0001c0001t0003g0145a0001c0001t0003g0210 | 2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2311+1506C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111293800 | ||||||
| chr13:111294088
|
T | C | 1 | a0001c0014t0001g0058 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2311+1794T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111294088 | ||||||
| chr13:111294097
|
A | T | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2311+1803A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111294097 | ||||||
| chr13:111294226
|
G | A | 6 | a0001c0001t0002g0099a0001c0003t0001g0142a0001c0003t0003g0021others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2311+1932G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111294226 | ||||||
| chr13:111294304
|
C | T | 47 | a0001c0001t0002g0029a0001c0001t0002g0156a0001c0001t0003g0087others(44): Show | 47 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.2311+2010C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111294304 | ||||||
| chr13:111294385
|
C | T | 1 | a0001c0002t0002g0155 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2311+2091C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111294385 | ||||||
| chr13:111294661
|
C | G | 1 | a0001c0001t0002g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2311+2367C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111294661 | ||||||
| chr13:111294826
|
T | G | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2311+2532T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111294826 | ||||||
| chr13:111294882
|
G | A | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2311+2588G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111294882 | ||||||
| chr13:111294897
|
A | G | 7 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(4): Show | 7 | HG02809.hp1 HG02818.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2311+2603A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111294897 | ||||||
| chr13:111294953
|
A | G | 4 | a0001c0001t0003g0178a0001c0001t0003g0216a0001c0001t0003g0262others(1): Show | 4 | HG00140.hp1 HG01099.hp1 HG01928.hp2 others(1): Show |
intron_variant | MODIFIER | c.2311+2659A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111294953 | ||||||
| chr13:111294964
|
TA | T | 6 | a0001c0001t0007g0004a0001c0001t0007g0009a0001c0001t0007g0028others(3): Show | 6 | HG01884.hp2 HG02055.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2311+2672delA | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr13 | 111294964 | |||||
| chr13:111295147
|
A | T | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2311+2853A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111295147 | ||||||
| chr13:111295196
|
C | T | 3 | a0001c0002t0010g0081a0001c0002t0010g0159a0001c0002t0010g0197 | 3 | NA18968.hp2 NA18999.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.2311+2902C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111295196 | ||||||
| chr13:111295272
|
T | C | 4 | a0001c0001t0029g0201a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18941.hp2 NA18957.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.2311+2978T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111295272 | ||||||
| chr13:111295378
|
G | A | 1 | a0001c0002t0002g0204 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2311+3084G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111295378 | ||||||
| chr13:111295390
|
T | C | 4 | a0001c0001t0016g0012a0001c0001t0016g0077a0001c0003t0001g0142others(1): Show | 4 | HG02280.hp2 HG02895.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2311+3096T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111295390 | ||||||
| chr13:111295489
|
T | C | 12 | a0001c0001t0005g0063a0001c0001t0005g0102a0001c0001t0005g0103others(9): Show | 12 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.2311+3195T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111295489 | ||||||
| chr13:111295576
|
A | AT | 7 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(4): Show | 7 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2311+3282_2311+328 others(5): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111295576 | ||||||
| chr13:111295578
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(4): Show | 7 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2311+3284G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111295578 | ||||||
| chr13:111295581
|
A | T | 7 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(4): Show | 7 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2311+3287A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111295581 | ||||||
| chr13:111295582
|
G | GC | 7 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(4): Show | 7 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2311+3288_2311+328 others(5): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111295582 | ||||||
| chr13:111295584
|
A | T | 7 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(4): Show | 7 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2311+3290A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111295584 | ||||||
| chr13:111295587
|
G | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(4): Show | 7 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2311+3293G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111295587 | ||||||
| chr13:111295588
|
A | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(4): Show | 7 | HG01243.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2311+3294A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111295588 | ||||||
| chr13:111295834
|
T | G | 1 | a0001c0001t0005g0212 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2311+3540T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111295834 | ||||||
| chr13:111295899
|
T | A | 6 | a0001c0001t0007g0094a0001c0001t0008g0003a0001c0001t0008g0015others(3): Show | 6 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2311+3605T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111295899 | ||||||
| chr13:111296094
|
G | A | 1 | a0001c0003t0019g0022 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2311+3800G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111296094 | ||||||
| chr13:111296129
|
G | T | 1 | a0001c0001t0007g0008 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2311+3835G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111296129 | ||||||
| chr13:111296325
|
A | C | 5 | a0001c0001t0016g0012a0001c0001t0016g0077a0001c0001t0016g0143others(2): Show | 5 | HG02280.hp2 HG02895.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2311+4031A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111296325 | ||||||
| chr13:111296446
|
C | T | 1 | a0001c0001t0009g0250 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2311+4152C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111296446 | ||||||
| chr13:111296476
|
C | T | 48 | a0001c0001t0002g0029a0001c0001t0002g0078a0001c0001t0002g0156others(45): Show | 48 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.2311+4182C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111296476 | ||||||
| chr13:111296557
|
A | G | 1 | a0001c0001t0001g0002 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2312-4191A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111296557 | ||||||
| chr13:111296675
|
T | C | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2312-4073T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111296675 | ||||||
| chr13:111296875
|
C | G | 6 | a0001c0001t0002g0011a0001c0001t0003g0025a0001c0001t0018g0020others(3): Show | 6 | HG02257.hp1 HG02451.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2312-3873C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111296875 | ||||||
| chr13:111296906
|
G | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(72): Show | 75 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.2312-3842G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111296906 | ||||||
| chr13:111297093
|
G | C | 4 | a0001c0002t0002g0147a0001c0002t0002g0148a0001c0002t0002g0149others(1): Show | 4 | HG01175.hp1 HG01361.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.2312-3655G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111297093 | ||||||
| chr13:111297094
|
C | T | 4 | a0001c0002t0002g0147a0001c0002t0002g0148a0001c0002t0002g0149others(1): Show | 4 | HG01175.hp1 HG01361.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.2312-3654C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111297094 | ||||||
| chr13:111297153
|
A | T | 1 | a0001c0001t0012g0001 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2312-3595A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111297153 | ||||||
| chr13:111297156
|
T | G | 1 | a0001c0001t0008g0017 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2312-3592T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111297156 | ||||||
| chr13:111297536
|
A | C | 1 | a0001c0005t0020g0117 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2312-3212A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111297536 | ||||||
| chr13:111297638
|
G | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0039others(10): Show | 13 | HG01891.hp1 HG02559.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.2312-3110G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111297638 | ||||||
| chr13:111297690
|
T | C | 7 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0008g0017others(4): Show | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2312-3058T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111297690 | ||||||
| chr13:111297739
|
C | T | 7 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0008g0017others(4): Show | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2312-3009C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111297739 | ||||||
| chr13:111297754
|
C | T | 13 | a0001c0001t0005g0063a0001c0001t0005g0102a0001c0001t0005g0103others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.2312-2994C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111297754 | ||||||
| chr13:111297816
|
G | A | 1 | a0001c0002t0002g0198 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2312-2932G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111297816 | ||||||
| chr13:111297921
|
C | T | 2 | a0001c0001t0003g0178a0001c0001t0003g0216 | 2 | HG00140.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.2312-2827C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111297921 | ||||||
| chr13:111297949
|
T | C | 7 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0008g0017others(4): Show | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2312-2799T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111297949 | ||||||
| chr13:111298345
|
T | C | 7 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0008g0017others(4): Show | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2312-2403T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111298345 | ||||||
| chr13:111298622
|
C | T | 34 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.2312-2126C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111298622 | ||||||
| chr13:111298705
|
T | C | 235 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(232): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.2312-2043T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111298705 | ||||||
| chr13:111298852
|
G | T | 3 | a0001c0001t0003g0104a0001c0001t0003g0108a0001c0001t0003g0128 | 3 | HG00099.hp2 HG01261.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.2312-1896G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111298852 | ||||||
| chr13:111298922
|
A | C | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2312-1826A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111298922 | ||||||
| chr13:111298964
|
C | T | 13 | a0001c0001t0005g0063a0001c0001t0005g0102a0001c0001t0005g0103others(10): Show | 13 | HG01071.hp1 HG01081.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.2312-1784C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111298964 | ||||||
| chr13:111299004
|
G | GA | 4 | a0001c0001t0018g0020a0001c0001t0018g0038a0001c0003t0003g0021others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2312-1743dupA | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr13 | 111299004 | |||||
| chr13:111299031
|
C | T | 4 | a0001c0001t0006g0263a0001c0001t0014g0153a0001c0001t0014g0161others(1): Show | 4 | HG01928.hp1 HG01943.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.2312-1717C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299031 | ||||||
| chr13:111299100
|
T | A | 2 | a0001c0001t0002g0011a0001c0001t0003g0025 | 2 | HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2312-1648T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299100 | ||||||
| chr13:111299221
|
T | C | 7 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0008g0017others(4): Show | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2312-1527T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299221 | ||||||
| chr13:111299292
|
C | T | 8 | a0001c0001t0011g0006a0001c0001t0011g0007a0001c0001t0011g0055others(5): Show | 8 | HG01884.hp1 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2312-1456C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299292 | ||||||
| chr13:111299324
|
G | T | 1 | a0001c0001t0006g0083 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2312-1424G>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299324 | ||||||
| chr13:111299337
|
A | AT | 121 | a0001c0001t0001g0005a0001c0001t0001g0137a0001c0001t0002g0029others(118): Show | 121 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.2312-1388dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr13 | 111299337 | |||||
| chr13:111299337
|
A | ATT | 22 | a0001c0001t0002g0011a0001c0001t0003g0024a0001c0001t0003g0025others(19): Show | 22 | HG00597.hp2 HG01192.hp1 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.2312-1389_2312-138 others(6): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | INFO_REALIGN_3_PRIME | chr13 | 111299337 | |||||
| chr13:111299346
|
T | TG | 7 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0008g0017others(4): Show | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2312-1402_2312-140 others(5): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299346 | ||||||
| chr13:111299351
|
T | A | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2312-1397T>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299351 | ||||||
| chr13:111299368
|
A | T | 4 | a0001c0001t0001g0160a0001c0001t0001g0195a0001c0001t0001g0196others(1): Show | 4 | NA18974.hp1 NA19068.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.2312-1380A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299368 | ||||||
| chr13:111299382
|
G | A | 7 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0008g0017others(4): Show | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2312-1366G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299382 | ||||||
| chr13:111299470
|
G | A | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2312-1278G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299470 | ||||||
| chr13:111299481
|
T | G | 3 | a0001c0001t0003g0107a0001c0001t0003g0136a0001c0001t0003g0215 | 3 | HG01891.hp2 HG02145.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2312-1267T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299481 | ||||||
| chr13:111299487
|
C | T | 1 | a0001c0002t0031g0130 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2312-1261C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299487 | ||||||
| chr13:111299488
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2312-1260G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299488 | ||||||
| chr13:111299559
|
G | A | 3 | a0001c0001t0002g0091a0001c0001t0002g0099a0001c0015t0002g0023 | 3 | HG03130.hp1 HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.2312-1189G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299559 | ||||||
| chr13:111299575
|
C | T | 1 | a0001c0002t0002g0060 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2312-1173C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299575 | ||||||
| chr13:111299595
|
G | A | 57 | a0001c0001t0002g0011a0001c0001t0002g0029a0001c0001t0002g0078others(54): Show | 57 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.2312-1153G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299595 | ||||||
| chr13:111299612
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0096 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2312-1136G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299612 | ||||||
| chr13:111299631
|
G | C | 7 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0008g0017others(4): Show | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2312-1117G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299631 | ||||||
| chr13:111299641
|
T | C | 7 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0008g0017others(4): Show | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2312-1107T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299641 | ||||||
| chr13:111299768
|
C | T | 4 | a0001c0001t0029g0201a0001c0002t0021g0255a0001c0002t0021g0256others(1): Show | 4 | NA18941.hp2 NA18957.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.2312-980C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299768 | ||||||
| chr13:111299824
|
C | A | 5 | a0001c0001t0016g0012a0001c0001t0016g0077a0001c0001t0016g0143others(2): Show | 5 | HG01167.hp2 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2312-924C>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299824 | ||||||
| chr13:111299870
|
A | T | 1 | a0007c0010t0001g0095 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2312-878A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299870 | ||||||
| chr13:111299893
|
T | C | 72 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(69): Show | 72 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.2312-855T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299893 | ||||||
| chr13:111299936
|
A | T | 1 | a0001c0001t0003g0088 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2312-812A>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299936 | ||||||
| chr13:111299947
|
A | C | 52 | a0001c0001t0002g0029a0001c0001t0002g0078a0001c0001t0002g0156others(49): Show | 52 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.2312-801A>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299947 | ||||||
| chr13:111299990
|
T | G | 1 | a0001c0001t0003g0240 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2312-758T>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111299990 | ||||||
| chr13:111300137
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2312-611G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111300137 | ||||||
| chr13:111300428
|
A | G | 7 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0008g0017others(4): Show | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2312-320A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111300428 | ||||||
| chr13:111300482
|
G | C | 3 | a0001c0001t0009g0258a0001c0001t0009g0259a0001c0001t0009g0260 | 3 | NA19000.hp1 NA19005.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.2312-266G>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111300482 | ||||||
| chr13:111300505
|
G | A | 3 | a0001c0001t0001g0106a0001c0005t0020g0117a0001c0005t0020g0118 | 3 | HG00639.hp2 HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2312-243G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111300505 | ||||||
| chr13:111300545
|
G | A | 7 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0008g0017others(4): Show | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2312-203G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 19/21 | chr13 | 111300545 | ||||||
| chr13:111300934
|
A | G | 2 | a0001c0001t0002g0011a0001c0001t0003g0025 | 2 | HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2411+87A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 20/21 | chr13 | 111300934 | ||||||
| chr13:111300938
|
C | G | 1 | a0001c0002t0002g0257 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2411+91C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 20/21 | chr13 | 111300938 | ||||||
| chr13:111300970
|
C | T | 24 | a0001c0001t0003g0087a0001c0001t0003g0088a0001c0001t0003g0089others(21): Show | 24 | HG00099.hp2 HG00597.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.2411+123C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 20/21 | chr13 | 111300970 | ||||||
| chr13:111301042
|
G | A | 1 | a0001c0001t0013g0162 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2411+195G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 20/21 | chr13 | 111301042 | ||||||
| chr13:111301195
|
C | T | 7 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0008g0017others(4): Show | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2412-283C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 20/21 | chr13 | 111301195 | ||||||
| chr13:111301278
|
G | A | 209 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.2412-200G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 20/21 | chr13 | 111301278 | ||||||
| chr13:111301378
|
G | A | 2 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | HG01243.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2412-100G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 20/21 | chr13 | 111301378 | ||||||
| chr13:111301455
|
G | A | 7 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0008g0017others(4): Show | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2412-23G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 20/21 | chr13 | 111301455 | ||||||
| chr13:111301536
|
C | T | 1 | a0001c0001t0006g0268 | 1 | HG01346.hp2 | splice_region_variant&intron_variant | LOW | c.2466+4C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111301536 | ||||||
| chr13:111301556
|
T | C | 114 | a0001c0001t0002g0029a0001c0001t0002g0078a0001c0001t0002g0091others(111): Show | 114 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.2466+24T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111301556 | ||||||
| chr13:111301721
|
C | T | 50 | a0001c0001t0002g0029a0001c0001t0002g0078a0001c0001t0002g0156others(47): Show | 50 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2466+189C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111301721 | ||||||
| chr13:111301783
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2466+251T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111301783 | ||||||
| chr13:111302005
|
C | CT | 8 | a0001c0001t0001g0084a0001c0001t0005g0062a0001c0001t0029g0201others(5): Show | 8 | HG01192.hp1 HG02257.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.2466+483dupT | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr13 | 111302005 | |||||
| chr13:111302111
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0096 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2466+579G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111302111 | ||||||
| chr13:111302209
|
T | C | 247 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(244): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.2466+677T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111302209 | ||||||
| chr13:111302287
|
G | A | 65 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0039others(62): Show | 65 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.2467-704G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111302287 | ||||||
| chr13:111302399
|
T | C | 7 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0008g0017others(4): Show | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2467-592T>C | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111302399 | ||||||
| chr13:111302550
|
C | T | 7 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0008g0017others(4): Show | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2467-441C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111302550 | ||||||
| chr13:111302579
|
C | T | 1 | a0004c0017t0003g0120 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2467-412C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111302579 | ||||||
| chr13:111302593
|
G | A | 5 | a0001c0001t0016g0012a0001c0001t0016g0077a0001c0001t0016g0143others(2): Show | 5 | HG01167.hp2 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2467-398G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111302593 | ||||||
| chr13:111302691
|
G | A | 1 | a0001c0002t0002g0206 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2467-300G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111302691 | ||||||
| chr13:111302722
|
C | T | 1 | a0006c0019t0002g0175 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2467-269C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111302722 | ||||||
| chr13:111302764
|
C | G | 2 | a0001c0001t0001g0173a0001c0001t0001g0205 | 2 | HG01952.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.2467-227C>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111302764 | ||||||
| chr13:111302789
|
A | G | 7 | a0001c0001t0008g0003a0001c0001t0008g0015a0001c0001t0008g0017others(4): Show | 7 | HG01109.hp1 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2467-202A>G | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111302789 | ||||||
| chr13:111302792
|
G | A | 1 | a0001c0001t0002g0099 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2467-199G>A | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111302792 | ||||||
| chr13:111302817
|
C | T | 4 | a0001c0001t0018g0020a0001c0001t0018g0038a0001c0003t0003g0021others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2467-174C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111302817 | ||||||
| chr13:111302944
|
C | T | 2 | a0001c0001t0008g0035a0001c0016t0008g0227 | 2 | NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2467-47C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111302944 | ||||||
| chr13:111302946
|
C | T | 1 | a0001c0002t0002g0148 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2467-45C>T | ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 21/21 | chr13 | 111302946 |