| geneid | 9693 |
|---|---|
| ensemblid | ENSG00000109756.10 |
| hgncid | 16854 |
| symbol | RAPGEF2 |
| name | Rap guanine nucleotide exchange factor 2 |
| refseq_nuc | NM_001394067.2 |
| refseq_prot | NP_001380996.1 |
| ensembl_nuc | ENST00000691494.1 |
| ensembl_prot | ENSP00000510694.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 159103079 |
| end | 159360173 |
| strand | + |
| ver | v1.2 |
| region | chr4:159103079-159360173 |
| region5000 | chr4:159098079-159365173 |
| regionname0 | RAPGEF2_chr4_159103079_159360173 |
| regionname5000 | RAPGEF2_chr4_159098079_159365173 |
| 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 | 1660 | 193 | 88 | 48 | 29 | 8 | 18 | 14 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0002 | 0/0 | 1660 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| 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 | 4983 | 99 | 50 | 17 | 21 | 2 | 8 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| c0002 | 0/1 | 4983 | 71 | 20 | 28 | 7 | 5 | 10 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| c0003 | 0/0 | 4983 | 12 | 11 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| c0004 | 0/0 | 4983 | 2 | 0 | 1 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| c0005 | 0/0 | 4983 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| c0006 | 0/0 | 4983 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| c0007 | 0/0 | 4983 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| c0008 | 0/0 | 4983 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| c0009 | 0/0 | 4983 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| c0010 | 0/0 | 4983 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| c0011 | 0/0 | 4983 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| 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 | 0/1 | 3117 | 46 | 7 | 22 | 6 | 3 | 7 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0002 | 0/0 | 3120 | 43 | 8 | 12 | 14 | 2 | 7 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0003 | 0/0 | 3120 | 22 | 11 | 5 | 1 | 2 | 3 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0004 | 0/0 | 3119 | 12 | 12 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0005 | 1/0 | 3119 | 9 | 7 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0006 | 0/0 | 3123 | 9 | 0 | 3 | 6 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0007 | 0/0 | 3118 | 6 | 5 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0008 | 0/0 | 3119 | 6 | 3 | 1 | 2 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0009 | 0/0 | 3118 | 4 | 4 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0010 | 0/0 | 3121 | 4 | 4 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0011 | 0/0 | 3120 | 3 | 3 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0012 | 0/0 | 3122 | 3 | 3 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0013 | 0/0 | 3122 | 3 | 3 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0014 | 0/0 | 3119 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0015 | 0/0 | 3123 | 2 | 1 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0016 | 0/0 | 3120 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0017 | 0/0 | 3119 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0018 | 0/0 | 3117 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0019 | 0/0 | 3119 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0020 | 0/0 | 3120 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0021 | 0/0 | 3119 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0022 | 0/0 | 3118 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0023 | 0/0 | 3118 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0024 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0025 | 0/0 | 3118 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0026 | 0/0 | 3117 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0027 | 0/0 | 3122 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0028 | 0/0 | 3123 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0029 | 0/0 | 3122 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0030 | 0/0 | 3117 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0031 | 0/0 | 3118 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0032 | 0/0 | 3120 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0033 | 0/0 | 3119 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| t0034 | 0/0 | 3119 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| 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 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| 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 | 4983 | 99 | 50 | 17 | 21 | 2 | 8 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0002 | 0/1 | 4983 | 71 | 20 | 28 | 7 | 5 | 10 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0003 | 0/0 | 4983 | 12 | 11 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0004 | 0/0 | 4983 | 2 | 0 | 1 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0005 | 0/0 | 4983 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0006 | 0/0 | 4983 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0007 | 0/0 | 4983 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0008 | 0/0 | 4983 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0010 | 0/0 | 4983 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0011 | 0/0 | 4983 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0002c0009 | 0/0 | 4983 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 8102 | 40 | 8 | 11 | 12 | 2 | 7 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0004 | 0/0 | 8101 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0005 | 1/0 | 8101 | 8 | 6 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0006 | 0/0 | 8105 | 9 | 0 | 3 | 6 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0007 | 0/0 | 8100 | 6 | 5 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0008 | 0/0 | 8101 | 6 | 3 | 1 | 2 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0009 | 0/0 | 8100 | 4 | 4 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0010 | 0/0 | 8103 | 4 | 4 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0011 | 0/0 | 8102 | 3 | 3 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0013 | 0/0 | 8104 | 3 | 3 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0015 | 0/0 | 8105 | 2 | 1 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0020 | 0/0 | 8102 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0021 | 0/0 | 8101 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0023 | 0/0 | 8100 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0024 | 0/0 | 8102 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0025 | 0/0 | 8100 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0026 | 0/0 | 8099 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0027 | 0/0 | 8104 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0028 | 0/0 | 8105 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0029 | 0/0 | 8104 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0031 | 0/0 | 8100 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0033 | 0/0 | 8101 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0001t0034 | 0/0 | 8101 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0002t0001 | 0/1 | 8099 | 45 | 7 | 21 | 6 | 3 | 7 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0002t0003 | 0/0 | 8102 | 21 | 11 | 5 | 1 | 1 | 3 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0002t0012 | 0/0 | 8104 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0002t0018 | 0/0 | 8099 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0002t0022 | 0/0 | 8100 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0002t0030 | 0/0 | 8099 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0003t0004 | 0/0 | 8101 | 10 | 10 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0003t0017 | 0/0 | 8101 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0003t0019 | 0/0 | 8101 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0004t0001 | 0/0 | 8099 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0004t0003 | 0/0 | 8102 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0005t0005 | 0/0 | 8101 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0005t0012 | 0/0 | 8104 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0006t0014 | 0/0 | 8101 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0007t0016 | 0/0 | 8102 | 2 | 2 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0008t0002 | 0/0 | 8102 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0010t0002 | 0/0 | 8102 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0001c0011t0032 | 0/0 | 8102 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| a0002c0009t0002 | 0/0 | 8102 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | copy fasta | chr4 | 159098079 | 159365173 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0005g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0005g0147 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0006g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0006g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0006g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0006g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0007g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0007g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0008g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0008g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0008g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0008g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0008g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0009g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0010g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0010g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0010g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0010g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0011g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0011g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0011g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0013g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0013g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0013g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0015g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0015g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0020g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0021g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0023g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0024g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0025g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0026g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0027g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0028g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0029g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0031g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0033g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0001t0034g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0012g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0012g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0018g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0022g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0002t0030g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0003t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0003t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0003t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0003t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0003t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0003t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0003t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0003t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0003t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0003t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0003t0017g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0003t0019g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0004t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0004t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0005t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0005t0012g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0006t0014g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0006t0014g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0007t0016g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0007t0016g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0008t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0010t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0001c0011t0032g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| a0002c0009t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0003 | g0185 | EUR | GBR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0108 | EUR | GBR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0088 | EUR | FIN | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00280 | hp2 | a0001 | c0004 | t0003 | g0159 | EUR | FIN | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | CHS | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | CHS | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | CHS | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | CHS | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | CHS | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0187 | EAS | CHS | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0126 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0056 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00735 | hp1 | a0001 | c0002 | t0018 | g0148 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0107 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0038 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0102 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01081 | hp1 | a0001 | c0001 | t0006 | g0170 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01081 | hp2 | a0001 | c0003 | t0017 | g0117 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01099 | hp1 | a0001 | c0002 | t0030 | g0137 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01099 | hp2 | a0001 | c0001 | t0015 | g0191 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0184 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0039 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0143 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0183 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01167 | hp2 | a0001 | c0008 | t0002 | g0119 | AMR | PUR | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | CLM | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0111 | AMR | CLM | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01261 | hp2 | a0001 | c0002 | t0003 | g0150 | AMR | CLM | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01361 | hp1 | a0001 | c0002 | t0003 | g0189 | AMR | CLM | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | CLM | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | CLM | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | CLM | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01516 | hp1 | a0001 | c0002 | t0022 | g0106 | EUR | IBS | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0134 | EUR | IBS | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0133 | EUR | IBS | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0079 | EUR | IBS | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01884 | hp1 | a0001 | c0007 | t0016 | g0140 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01884 | hp2 | a0001 | c0001 | t0010 | g0165 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01891 | hp1 | a0001 | c0001 | t0015 | g0190 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0082 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01934 | hp1 | a0001 | c0004 | t0001 | g0020 | AMR | PEL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PEL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PEL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01943 | hp2 | a0001 | c0001 | t0008 | g0112 | AMR | PEL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01978 | hp1 | a0001 | c0002 | t0003 | g0188 | AMR | PEL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0052 | AMR | PEL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01981 | hp1 | a0001 | c0002 | t0003 | g0168 | AMR | PEL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PEL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PEL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0054 | AMR | PEL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02040 | hp1 | a0001 | c0001 | t0006 | g0161 | EAS | KHV | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02055 | hp1 | a0001 | c0003 | t0004 | g0063 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02055 | hp2 | a0001 | c0002 | t0003 | g0008 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02074 | hp1 | a0001 | c0010 | t0002 | g0065 | EAS | KHV | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02129 | hp1 | a0001 | c0001 | t0006 | g0163 | EAS | KHV | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02145 | hp1 | a0001 | c0003 | t0004 | g0080 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0041 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02155 | hp1 | a0002 | c0009 | t0002 | g0011 | EAS | CDX | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0153 | EAS | CDX | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02165 | hp1 | a0001 | c0001 | t0008 | g0067 | EAS | CDX | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CDX | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02257 | hp1 | a0001 | c0011 | t0032 | g0114 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02258 | hp1 | a0001 | c0002 | t0003 | g0160 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02280 | hp2 | a0001 | c0001 | t0011 | g0021 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02451 | hp1 | a0001 | c0002 | t0003 | g0182 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0094 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02602 | hp1 | a0001 | c0001 | t0020 | g0120 | SAS | PJL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0046 | SAS | PJL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02615 | hp1 | a0001 | c0003 | t0004 | g0068 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0162 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0138 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02622 | hp2 | a0001 | c0001 | t0028 | g0167 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02630 | hp1 | a0001 | c0001 | t0024 | g0087 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02630 | hp2 | a0001 | c0003 | t0004 | g0064 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02647 | hp1 | a0001 | c0001 | t0013 | g0084 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02647 | hp2 | a0001 | c0001 | t0009 | g0146 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0180 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02723 | hp1 | a0001 | c0001 | t0023 | g0073 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02723 | hp2 | a0001 | c0002 | t0003 | g0178 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02809 | hp1 | a0001 | c0002 | t0012 | g0151 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02818 | hp1 | a0001 | c0001 | t0010 | g0155 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0051 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02886 | hp2 | a0001 | c0001 | t0010 | g0164 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0128 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02896 | hp2 | a0001 | c0003 | t0004 | g0047 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02897 | hp1 | a0001 | c0002 | t0003 | g0172 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02897 | hp2 | a0001 | c0003 | t0004 | g0061 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02922 | hp1 | a0001 | c0001 | t0033 | g0113 | AFR | ESN | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02922 | hp2 | a0001 | c0003 | t0019 | g0135 | AFR | ESN | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02970 | hp1 | a0001 | c0001 | t0021 | g0028 | AFR | ESN | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0023 | AFR | ESN | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0070 | AFR | ESN | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02976 | hp2 | a0001 | c0007 | t0016 | g0141 | AFR | ESN | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03017 | hp1 | a0001 | c0002 | t0003 | g0181 | SAS | PJL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0018 | SAS | PJL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03041 | hp1 | a0001 | c0003 | t0004 | g0072 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0157 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0086 | AFR | MSL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0077 | AFR | MSL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ESN | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03130 | hp2 | a0001 | c0006 | t0014 | g0026 | AFR | ESN | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03139 | hp1 | a0001 | c0002 | t0012 | g0156 | AFR | ESN | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03139 | hp2 | a0001 | c0001 | t0034 | g0115 | AFR | ESN | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | ESN | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03195 | hp2 | a0001 | c0002 | t0003 | g0166 | AFR | ESN | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03209 | hp1 | a0001 | c0001 | t0025 | g0081 | AFR | MSL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03209 | hp2 | a0001 | c0006 | t0014 | g0036 | AFR | MSL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | MSL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03225 | hp2 | a0001 | c0005 | t0005 | g0016 | AFR | MSL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0127 | AFR | MSL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0035 | AFR | MSL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0152 | SAS | PJL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0139 | AFR | ESN | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0078 | AFR | ESN | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03540 | hp1 | a0001 | c0001 | t0029 | g0002 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0059 | AFR | GWD | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | MSL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03579 | hp2 | a0001 | c0005 | t0012 | g0105 | AFR | MSL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0014 | SAS | PJL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03834 | hp1 | a0001 | c0002 | t0003 | g0176 | SAS | BEB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | STU | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0053 | SAS | STU | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | STU | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG04199 | hp2 | a0001 | c0002 | t0003 | g0174 | SAS | STU | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | STU | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | STU | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA18522 | hp1 | a0001 | c0001 | t0027 | g0104 | AFR | YRI | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA18522 | hp2 | a0001 | c0001 | t0031 | g0116 | AFR | YRI | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA18906 | hp1 | a0001 | c0001 | t0026 | g0003 | AFR | YRI | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0193 | AFR | YRI | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA18944 | hp2 | a0001 | c0002 | t0003 | g0169 | EAS | JPT | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA18961 | hp1 | a0001 | c0001 | t0006 | g0177 | EAS | JPT | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA18986 | hp2 | a0001 | c0001 | t0008 | g0062 | EAS | JPT | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA19043 | hp1 | a0001 | c0003 | t0004 | g0045 | AFR | LWK | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0092 | AFR | LWK | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA19087 | hp2 | a0001 | c0001 | t0006 | g0175 | EAS | JPT | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA19240 | hp1 | a0001 | c0002 | t0003 | g0179 | AFR | YRI | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | YRI | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA20129 | hp1 | a0001 | c0001 | t0009 | g0058 | AFR | ASW | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA20129 | hp2 | a0001 | c0001 | t0013 | g0085 | AFR | ASW | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01123 | hp1 | a0001 | c0001 | t0007 | g0095 | AMR | CLM | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG01123 | hp2 | a0001 | c0002 | t0003 | g0173 | AMR | CLM | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02109 | hp1 | a0001 | c0002 | t0003 | g0136 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02109 | hp2 | a0001 | c0003 | t0004 | g0009 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0033 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02559 | hp1 | a0001 | c0002 | t0003 | g0186 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG02559 | hp2 | a0001 | c0001 | t0013 | g0083 | AFR | ACB | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0043 | AFR | USA | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| HG06807 | hp2 | a0001 | c0003 | t0004 | g0019 | AFR | USA | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA18955 | hp1 | a0001 | c0001 | t0005 | g0049 | EAS | JPT | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA18955 | hp2 | a0001 | c0001 | t0006 | g0171 | EAS | JPT | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | USA | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA20300 | hp2 | a0001 | c0002 | t0003 | g0192 | AFR | USA | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA21309 | hp1 | a0001 | c0001 | t0011 | g0022 | AFR | LWK | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0093 | AFR | LWK | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0100 | REF | REF | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0147 | REF | REF | RAPGEF2_chr4_159098079_159365173 | RAPGEF2 | chr4 | 159098079 | 159365173 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:159352816
|
C | T | 1 | a0002 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.3997C>T | p.Arg1333Cys | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 27/30 | 5081/8101 | 3997/4983 | 1333/1660 | chr4 | 159352816 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:159329953
|
G | A | 1 | a0001c0008 | 1 | HG01167.hp2 | synonymous_variant | LOW | c.1245G>A | p.Val415Val | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/30 | 2329/8101 | 1245/4983 | 415/1660 | chr4 | 159329953 | ||
| chr4:159331662
|
C | T | 1 | a0001c0011 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.1608C>T | p.Ile536Ile | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 15/30 | 2692/8101 | 1608/4983 | 536/1660 | chr4 | 159331662 | ||
| chr4:159339244
|
G | A | 1 | a0001c0004 | 2 | HG00280.hp2 HG01934.hp1 |
synonymous_variant | LOW | c.2424G>A | p.Pro808Pro | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/30 | 3508/8101 | 2424/4983 | 808/1660 | chr4 | 159339244 | ||
| chr4:159342988
|
C | T | 1 | a0001c0003 | 12 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
synonymous_variant | LOW | c.2928C>T | p.Asn976Asn | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 21/30 | 4012/8101 | 2928/4983 | 976/1660 | chr4 | 159342988 | ||
| chr4:159343351
|
C | T | 1 | a0001c0010 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.3201C>T | p.His1067His | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 22/30 | 4285/8101 | 3201/4983 | 1067/1660 | chr4 | 159343351 | ||
| chr4:159346940
|
C | T | 1 | a0001c0007 | 2 | HG01884.hp1 HG02976.hp2 |
synonymous_variant | LOW | c.3654C>T | p.Pro1218Pro | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/30 | 4738/8101 | 3654/4983 | 1218/1660 | chr4 | 159346940 | ||
| chr4:159346943
|
C | T | 1 | a0001c0006 | 2 | HG03130.hp2 HG03209.hp2 |
synonymous_variant | LOW | c.3657C>T | p.Ala1219Ala | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/30 | 4741/8101 | 3657/4983 | 1219/1660 | chr4 | 159346943 | ||
| chr4:159352692
|
T | G | 1 | a0001c0003 | 12 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
synonymous_variant | LOW | c.3873T>G | p.Thr1291Thr | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 27/30 | 4957/8101 | 3873/4983 | 1291/1660 | chr4 | 159352692 | ||
| chr4:159355959
|
G | A | 1 | a0001c0005 | 2 | HG03225.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.4758G>A | p.Pro1586Pro | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/30 | 5842/8101 | 4758/4983 | 1586/1660 | chr4 | 159355959 | ||
| chr4:159356124
|
C | T | 2 | a0001c0002a0001c0004 | 73 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(70): Show |
synonymous_variant | LOW | c.4923C>T | p.Pro1641Pro | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/30 | 6007/8101 | 4923/4983 | 1641/1660 | chr4 | 159356124 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:159103185
|
G | T | 5 | a0001c0001t0031a0001c0001t0033a0001c0001t0034others(2): Show | 6 | HG01884.hp1 HG02257.hp1 HG02922.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-978G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/30 | 978 | chr4 | 159103185 | |||||
| chr4:159103230
|
C | G | 1 | a0001c0001t0015 | 2 | HG01099.hp2 HG01891.hp1 |
5_prime_UTR_variant | MODIFIER | c.-933C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/30 | 933 | chr4 | 159103230 | |||||
| chr4:159103577
|
G | A | 1 | a0001c0003t0017 | 1 | HG01081.hp2 | 5_prime_UTR_variant | MODIFIER | c.-586G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/30 | 586 | chr4 | 159103577 | |||||
| chr4:159103740
|
A | G | 1 | a0001c0002t0030 | 1 | HG01099.hp1 | 5_prime_UTR_variant | MODIFIER | c.-423A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/30 | 423 | chr4 | 159103740 | |||||
| chr4:159103869
|
A | AGAG | 11 | a0001c0001t0006a0001c0001t0010a0001c0001t0013others(8): Show | 46 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(43): Show |
5_prime_UTR_variant | MODIFIER | c.-279_-277dupGGA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/30 | 276 | INFO_REALIGN_3_PRIME | chr4 | 159103869 | ||||
| chr4:159103901
|
T | C | 2 | a0001c0002t0018a0001c0003t0019 | 2 | HG00735.hp1 HG02922.hp2 |
5_prime_UTR_variant | MODIFIER | c.-262T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/30 | 262 | chr4 | 159103901 | |||||
| chr4:159103928
|
G | A | 1 | a0001c0001t0020 | 1 | HG02602.hp1 | 5_prime_UTR_variant | MODIFIER | c.-235G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/30 | 235 | chr4 | 159103928 | |||||
| chr4:159103959
|
C | A | 2 | a0001c0002t0018a0001c0003t0019 | 2 | HG00735.hp1 HG02922.hp2 |
5_prime_UTR_variant | MODIFIER | c.-204C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/30 | 204 | chr4 | 159103959 | |||||
| chr4:159104012
|
C | A | 1 | a0001c0001t0011 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
5_prime_UTR_variant | MODIFIER | c.-151C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/30 | 151 | chr4 | 159104012 | |||||
| chr4:159104124
|
C | A | 1 | a0001c0001t0027 | 1 | NA18522.hp1 | 5_prime_UTR_variant | MODIFIER | c.-39C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/30 | 39 | chr4 | 159104124 | |||||
| chr4:159104135
|
G | A | 1 | a0001c0006t0014 | 2 | HG03130.hp2 HG03209.hp2 |
5_prime_UTR_variant | MODIFIER | c.-28G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/30 | 28 | chr4 | 159104135 | |||||
| chr4:159358235
|
C | T | 1 | a0001c0001t0034 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*96C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 30/30 | 96 | chr4 | 159358235 | |||||
| chr4:159358580
|
C | T | 21 | a0001c0001t0004a0001c0001t0007a0001c0001t0008others(18): Show | 50 | HG01081.hp2 HG01123.hp1 HG01884.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*441C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 30/30 | 441 | chr4 | 159358580 | |||||
| chr4:159358666
|
T | G | 1 | a0001c0001t0021 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*527T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 30/30 | 527 | chr4 | 159358666 | |||||
| chr4:159358672
|
T | TA | 9 | a0001c0001t0002a0001c0001t0006a0001c0001t0011others(6): Show | 60 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*545dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 30/30 | 546 | INFO_REALIGN_3_PRIME | chr4 | 159358672 | ||||
| chr4:159358672
|
TA | T | 11 | a0001c0001t0009a0001c0001t0010a0001c0001t0025others(8): Show | 81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*545delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 30/30 | 545 | INFO_REALIGN_3_PRIME | chr4 | 159358672 | ||||
| chr4:159358824
|
C | T | 1 | a0001c0001t0026 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*685C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 30/30 | 685 | chr4 | 159358824 | |||||
| chr4:159359149
|
GT | G | 16 | a0001c0001t0004a0001c0001t0007a0001c0001t0013others(13): Show | 98 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1017delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 30/30 | 1017 | INFO_REALIGN_3_PRIME | chr4 | 159359149 | ||||
| chr4:159359367
|
A | G | 4 | a0001c0001t0008a0001c0001t0029a0001c0001t0033others(1): Show | 9 | HG01943.hp2 HG02145.hp2 HG02165.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1228A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 30/30 | 1228 | chr4 | 159359367 | |||||
| chr4:159359687
|
A | G | 1 | a0001c0001t0023 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1548A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 30/30 | 1548 | chr4 | 159359687 | |||||
| chr4:159359710
|
A | AT | 9 | a0001c0001t0004a0001c0001t0013a0001c0001t0024others(6): Show | 22 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1572dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 30/30 | 1573 | INFO_REALIGN_3_PRIME | chr4 | 159359710 | ||||
| chr4:159359813
|
T | C | 1 | a0001c0001t0025 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1674T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 30/30 | 1674 | chr4 | 159359813 | |||||
| chr4:159359814
|
G | A | 1 | a0001c0001t0027 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1675G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 30/30 | 1675 | chr4 | 159359814 | |||||
| chr4:159360048
|
G | A | 1 | a0001c0001t0033 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1909G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 30/30 | 1909 | chr4 | 159360048 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:159104256
|
C | T | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.69+25C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104256 | ||||||
| chr4:159104489
|
C | CGA | 18 | a0001c0001t0002g0025a0001c0001t0002g0029a0001c0001t0005g0024others(15): Show | 18 | HG00639.hp1 HG01071.hp2 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.69+294_69+295dupAG | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104489 | |||||
| chr4:159104489
|
C | CGAGA | 27 | a0001c0001t0002g0044a0001c0001t0002g0121a0001c0001t0002g0122others(24): Show | 27 | HG00558.hp1 HG00639.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.69+292_69+295dupAG others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104489 | |||||
| chr4:159104489
|
C | CGAGAGA | 24 | a0001c0001t0002g0109a0001c0001t0002g0110a0001c0001t0002g0118others(21): Show | 24 | HG00099.hp2 HG00642.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.69+290_69+295dupAG others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104489 | |||||
| chr4:159104489
|
C | CGAGAGAG others(1): Show |
15 | a0001c0001t0002g0057a0001c0001t0002g0060a0001c0001t0002g0096others(12): Show | 15 | HG00438.hp1 HG00438.hp2 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.69+288_69+295dupAG others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104489 | |||||
| chr4:159104489
|
C | CGAGAGAG others(3): Show |
8 | a0001c0001t0002g0088a0001c0001t0002g0089a0001c0001t0002g0090others(5): Show | 8 | HG00280.hp1 HG01496.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.69+286_69+295dupAG others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104489 | |||||
| chr4:159104489
|
C | CGAGAGAG others(5): Show |
8 | a0001c0001t0002g0066a0001c0001t0005g0086a0001c0001t0008g0067others(5): Show | 8 | HG02074.hp1 HG02165.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.69+284_69+295dupAG others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104489 | |||||
| chr4:159104489
|
C | CGAGAGAG others(7): Show |
3 | a0001c0001t0008g0070a0001c0002t0001g0069a0001c0003t0004g0068 | 3 | HG01433.hp1 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.69+282_69+295dupAG others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104489 | |||||
| chr4:159104489
|
C | CGAGAGAG others(9): Show |
2 | a0001c0001t0002g0071a0001c0001t0002g0079 | 2 | HG01517.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.69+280_69+295dupAG others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104489 | |||||
| chr4:159104489
|
C | CGAGAGAG others(11): Show |
1 | a0001c0001t0002g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.69+278_69+295dupAG others(16): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104489 | |||||
| chr4:159104489
|
C | CGAGAGAG others(15): Show |
1 | a0001c0001t0002g0074 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.69+274_69+295dupAG others(20): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104489 | |||||
| chr4:159104489
|
CGAGA | C | 4 | a0001c0001t0002g0154a0001c0001t0010g0155a0001c0002t0001g0157others(1): Show | 4 | HG02818.hp1 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+292_69+295delAG others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104489 | |||||
| chr4:159104489
|
CGAGAGA | C | 11 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0010g0162others(8): Show | 11 | HG00280.hp2 HG00597.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.69+290_69+295delAG others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104489 | |||||
| chr4:159104489
|
CGAGAGAG others(1): Show |
C | 24 | a0001c0001t0006g0170a0001c0001t0006g0171a0001c0001t0006g0175others(21): Show | 24 | HG00099.hp1 HG00597.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.69+288_69+295delAG others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104489 | |||||
| chr4:159104505
|
A | AGAGAGAG others(4): Show |
1 | a0001c0001t0004g0193 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+275_69+285dupGA others(9): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104505 | |||||
| chr4:159104515
|
A | AGAGAGAG others(15): Show |
1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.69+295_69+296insAG others(20): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104515 | |||||
| chr4:159104522
|
GAGAGGGA others(5): Show |
G | 1 | a0001c0002t0022g0106 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.69+296_69+307delGG others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104522 | |||||
| chr4:159104523
|
AGAGG | A | 4 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0029g0002others(1): Show | 4 | HG03540.hp1 HG03579.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+296_69+299delGG others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104523 | |||||
| chr4:159104525
|
AGG | A | 4 | a0001c0001t0026g0003a0001c0002t0001g0004a0001c0002t0001g0006others(1): Show | 4 | HG03239.hp1 HG04228.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+296_69+297delGG | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104525 | |||||
| chr4:159104526
|
G | GAGAGAGA others(4): Show |
1 | a0001c0001t0013g0083 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.69+295_69+296insAG others(9): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104526 | ||||||
| chr4:159104527
|
G | A | 74 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0025others(71): Show | 74 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.69+296G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104527 | ||||||
| chr4:159104532
|
G | C | 3 | a0001c0001t0002g0001a0001c0001t0026g0003a0001c0002t0001g0004 | 3 | HG03834.hp2 NA18906.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.69+301G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104532 | ||||||
| chr4:159104534
|
C | CAG | 3 | a0001c0001t0002g0088a0001c0001t0004g0193a0001c0002t0001g0108 | 3 | HG00099.hp2 HG00280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.69+322_69+323dupAG | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104534 | |||||
| chr4:159104534
|
C | G | 15 | a0001c0001t0002g0001a0001c0001t0007g0077a0001c0001t0007g0078others(12): Show | 15 | HG00738.hp1 HG01123.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.69+303C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104534 | ||||||
| chr4:159104534
|
CAG | C | 9 | a0001c0001t0002g0005a0001c0001t0002g0074a0001c0001t0002g0076others(6): Show | 9 | HG00558.hp2 HG00597.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+322_69+323delAG | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104534 | |||||
| chr4:159104536
|
G | C | 1 | a0001c0002t0001g0034 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.69+305G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104536 | ||||||
| chr4:159104537
|
A | G | 2 | a0001c0001t0007g0094a0001c0001t0007g0095 | 2 | HG01123.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.69+306A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104537 | ||||||
| chr4:159104538
|
G | C | 4 | a0001c0001t0009g0035a0001c0001t0011g0021a0001c0001t0011g0022others(1): Show | 4 | HG02280.hp2 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+307G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104538 | ||||||
| chr4:159104541
|
A | G | 2 | a0001c0001t0007g0082a0001c0001t0025g0081 | 2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.69+310A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104541 | ||||||
| chr4:159104543
|
A | G | 1 | a0001c0003t0004g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.69+312A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104543 | ||||||
| chr4:159104545
|
A | G | 2 | a0001c0001t0007g0077a0001c0001t0007g0078 | 2 | HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.69+314A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104545 | ||||||
| chr4:159104547
|
A | T | 1 | a0001c0002t0022g0106 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.69+316A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104547 | ||||||
| chr4:159104549
|
A | T | 3 | a0001c0002t0001g0153a0001c0002t0022g0106a0001c0004t0001g0020 | 3 | HG01516.hp1 HG01934.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.69+318A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104549 | ||||||
| chr4:159104551
|
A | AGT | 39 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(36): Show | 39 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.69+321_69+322insTG | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104551 | |||||
| chr4:159104551
|
A | AGTGT | 5 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(2): Show | 5 | HG00738.hp1 HG02559.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+321_69+322insTG others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104551 | |||||
| chr4:159104551
|
A | T | 33 | a0001c0001t0002g0015a0001c0001t0002g0029a0001c0001t0002g0044others(30): Show | 33 | HG00639.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.69+320A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104551 | ||||||
| chr4:159104553
|
A | AGAGAGAG others(17): Show |
1 | a0001c0001t0007g0077 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.69+323_69+324insAG others(22): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104553 | |||||
| chr4:159104553
|
A | AGAGAGAG others(15): Show |
1 | a0001c0003t0004g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.69+323_69+324insAG others(20): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104553 | |||||
| chr4:159104553
|
A | AGAGAGGG others(13): Show |
2 | a0001c0001t0007g0078a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.69+323_69+324insAG others(18): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104553 | |||||
| chr4:159104553
|
A | AGAGT | 2 | a0001c0001t0004g0194a0001c0003t0004g0045 | 2 | NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.69+323_69+324insAG others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104553 | |||||
| chr4:159104553
|
A | AGGGAGAG others(9): Show |
4 | a0001c0001t0007g0082a0001c0001t0007g0094a0001c0001t0007g0095others(1): Show | 4 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+323_69+324insGG others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104553 | |||||
| chr4:159104553
|
A | AGT | 23 | a0001c0001t0002g0025a0001c0001t0002g0057a0001c0001t0002g0060others(20): Show | 23 | HG00438.hp2 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.69+339_69+340dupGT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104553 | |||||
| chr4:159104553
|
A | AGTGT | 5 | a0001c0001t0005g0051a0001c0001t0008g0070a0001c0002t0001g0050others(2): Show | 5 | HG00735.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+337_69+340dupGT others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104553 | |||||
| chr4:159104553
|
A | T | 92 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(89): Show | 92 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.69+322A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104553 | ||||||
| chr4:159104554
|
G | A | 1 | a0001c0002t0001g0107 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.69+323G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104554 | ||||||
| chr4:159104555
|
T | A | 2 | a0001c0001t0009g0035a0001c0003t0004g0072 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.69+324T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104555 | ||||||
| chr4:159104557
|
T | A | 1 | a0001c0001t0009g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.69+326T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104557 | ||||||
| chr4:159104564
|
GTGTGTGT others(1): Show |
G | 2 | a0001c0001t0029g0002a0001c0002t0003g0008 | 2 | HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.69+341_69+348delAT others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159104564 | |||||
| chr4:159104616
|
C | T | 1 | a0001c0001t0005g0049 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.69+385C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104616 | ||||||
| chr4:159104894
|
A | C | 9 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+663A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104894 | ||||||
| chr4:159104948
|
G | A | 12 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(9): Show | 12 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.69+717G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159104948 | ||||||
| chr4:159105213
|
T | C | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+982T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159105213 | ||||||
| chr4:159105251
|
G | T | 1 | a0001c0002t0003g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.69+1020G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159105251 | ||||||
| chr4:159105279
|
A | C | 1 | a0001c0001t0005g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.69+1048A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159105279 | ||||||
| chr4:159105394
|
A | G | 38 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(35): Show | 38 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.69+1163A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159105394 | ||||||
| chr4:159105466
|
T | A | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+1235T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159105466 | ||||||
| chr4:159105498
|
G | T | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+1267G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159105498 | ||||||
| chr4:159105580
|
G | C | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+1349G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159105580 | ||||||
| chr4:159105631
|
A | G | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+1400A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159105631 | ||||||
| chr4:159105879
|
T | C | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+1648T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159105879 | ||||||
| chr4:159105993
|
A | T | 1 | a0001c0001t0002g0154 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.69+1762A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159105993 | ||||||
| chr4:159106072
|
C | T | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+1841C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159106072 | ||||||
| chr4:159106151
|
T | A | 1 | a0001c0001t0002g0149 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.69+1920T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159106151 | ||||||
| chr4:159106315
|
C | G | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.69+2084C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159106315 | ||||||
| chr4:159106652
|
A | G | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+2421A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159106652 | ||||||
| chr4:159106933
|
G | A | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+2702G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159106933 | ||||||
| chr4:159106955
|
GA | G | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+2725delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159106955 | ||||||
| chr4:159107080
|
A | G | 5 | a0001c0001t0002g0005a0001c0001t0011g0021a0001c0001t0011g0022others(2): Show | 5 | HG02280.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+2849A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159107080 | ||||||
| chr4:159107129
|
A | G | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+2898A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159107129 | ||||||
| chr4:159107315
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.69+3084G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159107315 | ||||||
| chr4:159107356
|
C | G | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.69+3125C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159107356 | ||||||
| chr4:159107600
|
T | G | 193 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.69+3369T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159107600 | ||||||
| chr4:159107660
|
A | T | 46 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0029others(43): Show | 46 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.69+3429A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159107660 | ||||||
| chr4:159107682
|
CTT | C | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+3452_69+3453del others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159107682 | ||||||
| chr4:159107694
|
C | A | 1 | a0001c0002t0003g0169 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.69+3463C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159107694 | ||||||
| chr4:159107717
|
G | A | 42 | a0001c0001t0002g0079a0001c0001t0002g0088a0001c0001t0002g0089others(39): Show | 42 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.69+3486G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159107717 | ||||||
| chr4:159107925
|
T | C | 6 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+3694T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159107925 | ||||||
| chr4:159108112
|
A | C | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+3881A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159108112 | ||||||
| chr4:159108131
|
A | G | 1 | a0001c0001t0002g0132 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.69+3900A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159108131 | ||||||
| chr4:159108190
|
C | A | 36 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0029others(33): Show | 36 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.69+3959C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159108190 | ||||||
| chr4:159108339
|
T | G | 2 | a0001c0001t0002g0010a0002c0009t0002g0011 | 2 | HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.69+4108T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159108339 | ||||||
| chr4:159108383
|
C | CT | 33 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0175others(30): Show | 33 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.69+4175dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159108383 | |||||
| chr4:159108383
|
C | CTT | 6 | a0001c0001t0015g0190a0001c0001t0015g0191a0001c0001t0028g0167others(3): Show | 6 | HG01099.hp2 HG01891.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+4174_69+4175dup others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159108383 | |||||
| chr4:159108383
|
CT | C | 9 | a0001c0001t0002g0109a0001c0001t0002g0149a0001c0001t0020g0120others(6): Show | 9 | HG00558.hp2 HG01167.hp2 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+4175delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159108383 | |||||
| chr4:159108387
|
T | C | 77 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(74): Show | 77 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.69+4156T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159108387 | ||||||
| chr4:159108388
|
T | C | 3 | a0001c0002t0001g0006a0001c0002t0001g0046a0001c0003t0004g0047 | 3 | HG02602.hp2 HG02896.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.69+4157T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159108388 | ||||||
| chr4:159108423
|
C | T | 2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.69+4192C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159108423 | ||||||
| chr4:159108448
|
C | T | 4 | a0001c0001t0004g0193a0001c0001t0005g0092a0001c0001t0005g0093others(1): Show | 4 | NA18906.hp2 NA19043.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+4217C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159108448 | ||||||
| chr4:159108485
|
A | G | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+4254A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159108485 | ||||||
| chr4:159108749
|
G | GAT | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+4527_69+4528dup others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159108749 | |||||
| chr4:159108783
|
G | T | 41 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.69+4552G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159108783 | ||||||
| chr4:159109242
|
G | A | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+5011G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159109242 | ||||||
| chr4:159109470
|
T | A | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.69+5239T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159109470 | ||||||
| chr4:159109693
|
A | G | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+5462A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159109693 | ||||||
| chr4:159109934
|
C | CCT | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+5704_69+5705ins others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159109934 | |||||
| chr4:159110311
|
G | C | 1 | a0001c0001t0024g0087 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.69+6080G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159110311 | ||||||
| chr4:159110324
|
A | G | 1 | a0001c0001t0002g0001 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.69+6093A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159110324 | ||||||
| chr4:159110417
|
A | G | 143 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.69+6186A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159110417 | ||||||
| chr4:159110503
|
T | G | 143 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.69+6272T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159110503 | ||||||
| chr4:159110557
|
A | T | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.69+6326A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159110557 | ||||||
| chr4:159110565
|
C | T | 5 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+6334C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159110565 | ||||||
| chr4:159110746
|
T | G | 1 | a0001c0001t0009g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.69+6515T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159110746 | ||||||
| chr4:159110902
|
A | ATATATT | 143 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.69+6675_69+6680dup others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159110902 | |||||
| chr4:159111083
|
G | A | 2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.69+6852G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159111083 | ||||||
| chr4:159111166
|
T | G | 192 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.69+6935T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159111166 | ||||||
| chr4:159111243
|
T | C | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+7012T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159111243 | ||||||
| chr4:159111334
|
C | T | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+7103C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159111334 | ||||||
| chr4:159111460
|
G | A | 1 | a0001c0004t0003g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.69+7229G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159111460 | ||||||
| chr4:159111487
|
A | G | 3 | a0001c0002t0003g0188a0001c0002t0003g0189a0001c0002t0003g0192 | 3 | HG01361.hp1 HG01978.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.69+7256A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159111487 | ||||||
| chr4:159112248
|
A | G | 1 | a0001c0003t0004g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.69+8017A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159112248 | ||||||
| chr4:159112379
|
A | AT | 17 | a0001c0001t0002g0001a0001c0001t0002g0060a0001c0001t0002g0071others(14): Show | 17 | HG00438.hp2 HG02074.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.69+8158dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159112379 | |||||
| chr4:159112596
|
T | C | 1 | a0001c0002t0003g0173 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.69+8365T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159112596 | ||||||
| chr4:159112760
|
G | A | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+8529G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159112760 | ||||||
| chr4:159112779
|
A | T | 1 | a0001c0001t0002g0057 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.69+8548A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159112779 | ||||||
| chr4:159112925
|
A | G | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+8694A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159112925 | ||||||
| chr4:159112930
|
T | C | 3 | a0001c0001t0002g0071a0001c0001t0009g0058a0001c0001t0009g0059 | 3 | HG02258.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.69+8699T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159112930 | ||||||
| chr4:159113100
|
G | T | 2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.69+8869G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159113100 | ||||||
| chr4:159113292
|
C | T | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+9061C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159113292 | ||||||
| chr4:159113373
|
T | C | 1 | a0001c0001t0005g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.69+9142T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159113373 | ||||||
| chr4:159113649
|
A | G | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+9418A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159113649 | ||||||
| chr4:159113690
|
C | G | 1 | a0001c0001t0002g0057 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.69+9459C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159113690 | ||||||
| chr4:159113740
|
C | CA | 7 | a0001c0001t0002g0074a0001c0001t0002g0076a0001c0001t0004g0194others(4): Show | 7 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+9530dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159113740 | |||||
| chr4:159113740
|
C | CAA | 9 | a0001c0001t0002g0005a0001c0001t0005g0086a0001c0001t0007g0077others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+9529_69+9530dup others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159113740 | |||||
| chr4:159113740
|
CA | C | 74 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0029others(71): Show | 74 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.69+9530delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159113740 | |||||
| chr4:159113740
|
CAA | C | 5 | a0001c0001t0005g0012a0001c0001t0008g0033a0001c0002t0001g0139others(2): Show | 5 | HG00735.hp1 HG02486.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+9529_69+9530del others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159113740 | |||||
| chr4:159113903
|
C | A | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+9672C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159113903 | ||||||
| chr4:159113951
|
G | A | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+9720G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159113951 | ||||||
| chr4:159113951
|
G | GTTTAT | 9 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+9733_69+9737dup others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159113951 | |||||
| chr4:159114119
|
AT | A | 6 | a0001c0001t0002g0142a0001c0001t0004g0193a0001c0001t0005g0024others(3): Show | 6 | HG01258.hp1 HG01891.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+9906delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159114119 | |||||
| chr4:159114120
|
T | G | 40 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.69+9889T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159114120 | ||||||
| chr4:159114121
|
T | G | 1 | a0001c0001t0015g0190 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.69+9890T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159114121 | ||||||
| chr4:159114138
|
C | T | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+9907C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159114138 | ||||||
| chr4:159114162
|
A | G | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+9931A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159114162 | ||||||
| chr4:159114345
|
G | T | 5 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(2): Show | 5 | HG02109.hp1 HG02559.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+10114G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159114345 | ||||||
| chr4:159114491
|
C | G | 1 | a0001c0004t0003g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.69+10260C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159114491 | ||||||
| chr4:159114625
|
T | C | 1 | a0001c0002t0003g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.69+10394T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159114625 | ||||||
| chr4:159114811
|
C | A | 1 | a0001c0001t0002g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.69+10580C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159114811 | ||||||
| chr4:159114822
|
T | C | 1 | a0001c0002t0001g0052 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.69+10591T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159114822 | ||||||
| chr4:159115041
|
C | T | 1 | a0001c0001t0002g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.69+10810C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159115041 | ||||||
| chr4:159115106
|
C | T | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+10875C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159115106 | ||||||
| chr4:159115500
|
T | A | 142 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.69+11269T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159115500 | ||||||
| chr4:159115553
|
AT | A | 179 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(176): Show | 179 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.69+11334delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159115553 | |||||
| chr4:159115553
|
ATT | A | 12 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(9): Show | 12 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.69+11333_69+11334d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159115553 | |||||
| chr4:159115875
|
G | T | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.69+11644G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159115875 | ||||||
| chr4:159115998
|
A | C | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.69+11767A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159115998 | ||||||
| chr4:159116125
|
A | G | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+11894A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159116125 | ||||||
| chr4:159116382
|
T | G | 142 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.69+12151T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159116382 | ||||||
| chr4:159116387
|
C | T | 9 | a0001c0001t0002g0071a0001c0001t0009g0058a0001c0001t0009g0059others(6): Show | 9 | HG02109.hp2 HG02258.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+12156C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159116387 | ||||||
| chr4:159116472
|
G | GT | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+12242dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159116472 | |||||
| chr4:159116879
|
A | G | 1 | a0001c0001t0002g0010 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.69+12648A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159116879 | ||||||
| chr4:159116887
|
G | C | 1 | a0001c0003t0017g0117 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.69+12656G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159116887 | ||||||
| chr4:159116974
|
CACACTGT others(1): Show |
C | 3 | a0001c0001t0026g0003a0001c0006t0014g0026a0001c0006t0014g0036 | 3 | HG03130.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.69+12746_69+12753d others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159116974 | |||||
| chr4:159117011
|
A | G | 81 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(78): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.69+12780A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159117011 | ||||||
| chr4:159117484
|
A | G | 6 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+13253A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159117484 | ||||||
| chr4:159117574
|
G | T | 81 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(78): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.69+13343G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159117574 | ||||||
| chr4:159117583
|
G | A | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+13352G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159117583 | ||||||
| chr4:159117583
|
G | GT | 7 | a0001c0001t0007g0077a0001c0001t0007g0082a0001c0001t0007g0094others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+13364dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159117583 | |||||
| chr4:159117585
|
T | G | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+13354T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159117585 | ||||||
| chr4:159117997
|
A | G | 41 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.69+13766A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159117997 | ||||||
| chr4:159118118
|
C | T | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.69+13887C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159118118 | ||||||
| chr4:159118226
|
G | GC | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+13996dupC | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159118226 | |||||
| chr4:159118259
|
C | G | 1 | a0001c0001t0009g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.69+14028C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159118259 | ||||||
| chr4:159118262
|
A | G | 1 | a0001c0001t0002g0130 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.69+14031A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159118262 | ||||||
| chr4:159118305
|
A | G | 1 | a0001c0010t0002g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.69+14074A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159118305 | ||||||
| chr4:159118343
|
A | G | 1 | a0001c0001t0002g0088 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.69+14112A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159118343 | ||||||
| chr4:159118397
|
C | T | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+14166C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159118397 | ||||||
| chr4:159118638
|
T | C | 9 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+14407T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159118638 | ||||||
| chr4:159118730
|
C | T | 1 | a0001c0002t0001g0157 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.69+14499C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159118730 | ||||||
| chr4:159118746
|
T | TG | 12 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(9): Show | 12 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.69+14516dupG | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159118746 | |||||
| chr4:159118763
|
G | T | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+14532G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159118763 | ||||||
| chr4:159118836
|
C | G | 10 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0004g0193others(7): Show | 10 | HG02630.hp1 HG02886.hp1 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+14605C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159118836 | ||||||
| chr4:159119007
|
C | T | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+14776C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159119007 | ||||||
| chr4:159119014
|
G | A | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+14783G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159119014 | ||||||
| chr4:159119026
|
G | A | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+14795G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159119026 | ||||||
| chr4:159119056
|
T | G | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+14825T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159119056 | ||||||
| chr4:159119172
|
G | A | 6 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+14941G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159119172 | ||||||
| chr4:159119585
|
T | G | 2 | a0001c0001t0028g0167a0001c0002t0003g0168 | 2 | HG01981.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.69+15354T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159119585 | ||||||
| chr4:159119616
|
G | A | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+15385G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159119616 | ||||||
| chr4:159119628
|
C | T | 1 | a0001c0001t0006g0187 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.69+15397C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159119628 | ||||||
| chr4:159119851
|
T | C | 1 | a0001c0002t0001g0013 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.69+15620T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159119851 | ||||||
| chr4:159119854
|
T | C | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+15623T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159119854 | ||||||
| chr4:159119925
|
T | C | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+15694T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159119925 | ||||||
| chr4:159120052
|
C | T | 1 | a0001c0004t0003g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.69+15821C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159120052 | ||||||
| chr4:159120229
|
A | G | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+15998A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159120229 | ||||||
| chr4:159120328
|
ACTT | A | 81 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(78): Show | 81 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.69+16101_69+16103d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159120328 | |||||
| chr4:159120425
|
T | C | 1 | a0001c0001t0002g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.69+16194T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159120425 | ||||||
| chr4:159120429
|
T | C | 1 | a0001c0001t0002g0029 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.69+16198T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159120429 | ||||||
| chr4:159120675
|
C | G | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+16444C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159120675 | ||||||
| chr4:159121095
|
T | G | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.69+16864T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159121095 | ||||||
| chr4:159121153
|
G | C | 142 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.69+16922G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159121153 | ||||||
| chr4:159121170
|
C | G | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+16939C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159121170 | ||||||
| chr4:159121240
|
A | G | 1 | a0001c0002t0001g0004 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.69+17009A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159121240 | ||||||
| chr4:159121481
|
C | G | 1 | a0001c0002t0001g0013 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.69+17250C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159121481 | ||||||
| chr4:159121561
|
A | G | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+17330A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159121561 | ||||||
| chr4:159121779
|
G | C | 12 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(9): Show | 12 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.69+17548G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159121779 | ||||||
| chr4:159121797
|
G | A | 1 | a0001c0002t0003g0188 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.69+17566G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159121797 | ||||||
| chr4:159121802
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.69+17571G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159121802 | ||||||
| chr4:159121874
|
C | CA | 50 | a0001c0001t0002g0005a0001c0001t0002g0154a0001c0001t0006g0161others(47): Show | 50 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.69+17656dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159121874 | |||||
| chr4:159121894
|
G | A | 6 | a0001c0001t0031g0116a0001c0001t0033g0113a0001c0001t0034g0115others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+17663G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159121894 | ||||||
| chr4:159121942
|
G | A | 6 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+17711G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159121942 | ||||||
| chr4:159122013
|
T | C | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+17782T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159122013 | ||||||
| chr4:159122023
|
A | C | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+17792A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159122023 | ||||||
| chr4:159122038
|
C | CA | 15 | a0001c0001t0002g0005a0001c0001t0002g0096a0001c0001t0002g0142others(12): Show | 15 | HG00735.hp2 HG01081.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.69+17831dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159122038 | |||||
| chr4:159122038
|
C | CAA | 9 | a0001c0001t0007g0078a0001c0001t0007g0082a0001c0001t0007g0094others(6): Show | 9 | HG01123.hp1 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+17830_69+17831d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159122038 | |||||
| chr4:159122038
|
CA | C | 77 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.69+17831delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159122038 | |||||
| chr4:159122038
|
CAA | C | 18 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0009g0058others(15): Show | 18 | HG00735.hp1 HG02109.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.69+17830_69+17831d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159122038 | |||||
| chr4:159122340
|
A | G | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+18109A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159122340 | ||||||
| chr4:159122347
|
C | T | 3 | a0001c0002t0003g0188a0001c0002t0003g0189a0001c0002t0003g0192 | 3 | HG01361.hp1 HG01978.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.69+18116C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159122347 | ||||||
| chr4:159122380
|
G | A | 33 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0029others(30): Show | 33 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.69+18149G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159122380 | ||||||
| chr4:159122518
|
C | A | 142 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.69+18287C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159122518 | ||||||
| chr4:159122693
|
G | C | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+18462G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159122693 | ||||||
| chr4:159122952
|
C | G | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+18721C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159122952 | ||||||
| chr4:159122979
|
TAAAC | T | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+18752_69+18755d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159122979 | |||||
| chr4:159122995
|
A | G | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+18764A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159122995 | ||||||
| chr4:159123023
|
TCTTC | T | 47 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.69+18796_69+18799d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159123023 | |||||
| chr4:159123472
|
G | A | 8 | a0001c0001t0005g0024a0001c0001t0026g0003a0001c0002t0001g0075others(5): Show | 8 | HG00597.hp1 HG01516.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+19241G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159123472 | ||||||
| chr4:159123578
|
G | A | 1 | a0001c0002t0003g0176 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.69+19347G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159123578 | ||||||
| chr4:159123611
|
T | C | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+19380T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159123611 | ||||||
| chr4:159123637
|
G | A | 2 | a0001c0001t0002g0089a0001c0001t0002g0110 | 2 | HG02129.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.69+19406G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159123637 | ||||||
| chr4:159123739
|
C | T | 3 | a0001c0002t0003g0188a0001c0002t0003g0189a0001c0002t0003g0192 | 3 | HG01361.hp1 HG01978.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.69+19508C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159123739 | ||||||
| chr4:159123772
|
C | T | 2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.69+19541C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159123772 | ||||||
| chr4:159123934
|
C | G | 1 | a0001c0002t0001g0152 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.69+19703C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159123934 | ||||||
| chr4:159124016
|
C | T | 2 | a0001c0003t0004g0064a0001c0003t0004g0068 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.69+19785C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159124016 | ||||||
| chr4:159124049
|
T | C | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+19818T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159124049 | ||||||
| chr4:159124058
|
G | A | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.69+19827G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159124058 | ||||||
| chr4:159124134
|
C | T | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+19903C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159124134 | ||||||
| chr4:159124161
|
G | A | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+19930G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159124161 | ||||||
| chr4:159124190
|
T | TC | 12 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(9): Show | 12 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.69+19960dupC | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159124190 | |||||
| chr4:159124854
|
T | C | 142 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.69+20623T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159124854 | ||||||
| chr4:159124942
|
T | G | 2 | a0001c0001t0006g0161a0001c0001t0006g0177 | 2 | HG02040.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.69+20711T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159124942 | ||||||
| chr4:159125034
|
TA | T | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+20804delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159125034 | ||||||
| chr4:159125119
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.69+20888C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159125119 | ||||||
| chr4:159125120
|
G | A | 47 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(44): Show | 47 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.69+20889G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159125120 | ||||||
| chr4:159125208
|
CAATCAAT others(1): Show |
C | 2 | a0001c0001t0005g0092a0001c0001t0005g0093 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.69+20990_69+20997d others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159125208 | |||||
| chr4:159125222
|
A | G | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+20991A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159125222 | ||||||
| chr4:159125231
|
T | C | 1 | a0001c0001t0021g0028 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.69+21000T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159125231 | ||||||
| chr4:159125394
|
G | A | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+21163G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159125394 | ||||||
| chr4:159125413
|
A | G | 36 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0029others(33): Show | 36 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.69+21182A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159125413 | ||||||
| chr4:159125426
|
G | C | 12 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(9): Show | 12 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.69+21195G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159125426 | ||||||
| chr4:159125438
|
C | T | 1 | a0001c0001t0007g0082 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.69+21207C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159125438 | ||||||
| chr4:159125619
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.69+21388A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159125619 | ||||||
| chr4:159125675
|
G | A | 1 | a0001c0001t0002g0130 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.69+21444G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159125675 | ||||||
| chr4:159125758
|
GA | G | 95 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(92): Show | 95 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.69+21541delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159125758 | |||||
| chr4:159125770
|
A | T | 11 | a0001c0001t0002g0005a0001c0001t0005g0051a0001c0001t0007g0077others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.69+21539A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159125770 | ||||||
| chr4:159125824
|
G | A | 1 | a0001c0001t0002g0149 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.69+21593G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159125824 | ||||||
| chr4:159125838
|
C | G | 1 | a0001c0001t0002g0131 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.69+21607C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159125838 | ||||||
| chr4:159125889
|
A | G | 4 | a0001c0001t0009g0035a0001c0001t0029g0002a0001c0002t0001g0018others(1): Show | 4 | HG02055.hp2 HG03017.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+21658A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159125889 | ||||||
| chr4:159126151
|
A | G | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+21920A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159126151 | ||||||
| chr4:159126364
|
C | A | 1 | a0001c0002t0003g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.69+22133C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159126364 | ||||||
| chr4:159126480
|
G | T | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+22249G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159126480 | ||||||
| chr4:159126527
|
G | GT | 41 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.69+22300dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159126527 | |||||
| chr4:159126531
|
T | A | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+22300T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159126531 | ||||||
| chr4:159126548
|
C | T | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+22317C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159126548 | ||||||
| chr4:159126589
|
C | T | 1 | a0001c0001t0002g0121 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.69+22358C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159126589 | ||||||
| chr4:159127020
|
TTTG | T | 7 | a0001c0001t0002g0066a0001c0001t0008g0062a0001c0001t0008g0067others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.69+22801_69+22803d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159127020 | |||||
| chr4:159127083
|
G | A | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+22852G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159127083 | ||||||
| chr4:159127282
|
C | T | 1 | a0001c0002t0001g0157 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.69+23051C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159127282 | ||||||
| chr4:159127349
|
C | T | 142 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.69+23118C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159127349 | ||||||
| chr4:159127517
|
T | C | 1 | a0001c0001t0015g0190 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.69+23286T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159127517 | ||||||
| chr4:159127546
|
C | T | 42 | a0001c0001t0002g0044a0001c0001t0006g0161a0001c0001t0006g0163others(39): Show | 42 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.69+23315C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159127546 | ||||||
| chr4:159127599
|
C | T | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+23368C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159127599 | ||||||
| chr4:159127611
|
C | T | 4 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(1): Show | 4 | HG02886.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+23380C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159127611 | ||||||
| chr4:159127665
|
G | A | 1 | a0001c0003t0004g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.69+23434G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159127665 | ||||||
| chr4:159127737
|
AT | A | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+23507delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159127737 | ||||||
| chr4:159127786
|
T | A | 1 | a0001c0002t0001g0139 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.69+23555T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159127786 | ||||||
| chr4:159127840
|
G | C | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+23609G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159127840 | ||||||
| chr4:159128138
|
G | C | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+23907G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159128138 | ||||||
| chr4:159128214
|
A | G | 18 | a0001c0001t0002g0001a0001c0001t0002g0025a0001c0001t0002g0060others(15): Show | 18 | HG00438.hp2 HG02074.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.69+23983A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159128214 | ||||||
| chr4:159128234
|
G | T | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+24003G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159128234 | ||||||
| chr4:159128323
|
A | C | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+24092A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159128323 | ||||||
| chr4:159128355
|
A | G | 1 | a0001c0002t0001g0046 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.69+24124A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159128355 | ||||||
| chr4:159128549
|
A | AGT | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+24319_69+24320d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159128549 | |||||
| chr4:159128555
|
T | TAGAA | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+24324_69+24325i others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159128555 | ||||||
| chr4:159128556
|
T | A | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+24325T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159128556 | ||||||
| chr4:159128557
|
C | T | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+24326C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159128557 | ||||||
| chr4:159128781
|
TAAA | T | 4 | a0001c0001t0007g0127a0001c0002t0001g0128a0001c0002t0001g0129others(1): Show | 4 | HG02280.hp1 HG02622.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+24551_69+24553d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159128781 | ||||||
| chr4:159128916
|
TGG | T | 49 | a0001c0001t0002g0074a0001c0001t0004g0193a0001c0001t0005g0086others(46): Show | 49 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.69+24690_69+24691d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159128916 | |||||
| chr4:159128919
|
GGGGTGTG others(3): Show |
G | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+24690_69+24699d others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159128919 | |||||
| chr4:159128921
|
G | T | 87 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(84): Show | 87 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.69+24690G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159128921 | ||||||
| chr4:159128940
|
GTGTGTAT others(5): Show |
G | 1 | a0001c0001t0007g0078 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.69+24711_69+24722d others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159128940 | |||||
| chr4:159128942
|
G | A | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+24711G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159128942 | ||||||
| chr4:159128942
|
G | GTATA | 2 | a0001c0001t0027g0104a0001c0002t0003g0136 | 2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.69+24712_69+24713i others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159128942 | |||||
| chr4:159128944
|
G | A | 48 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0029others(45): Show | 48 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.69+24713G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159128944 | ||||||
| chr4:159128944
|
GTATATA | G | 6 | a0001c0001t0007g0077a0001c0001t0007g0082a0001c0001t0007g0094others(3): Show | 6 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+24726_69+24731d others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159128944 | |||||
| chr4:159128946
|
A | G | 9 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0164others(6): Show | 9 | HG01361.hp1 HG01884.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+24715A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159128946 | ||||||
| chr4:159128952
|
A | G | 6 | a0001c0001t0007g0077a0001c0001t0007g0082a0001c0001t0007g0094others(3): Show | 6 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+24721A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159128952 | ||||||
| chr4:159129049
|
A | T | 1 | a0001c0001t0002g0103 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.69+24818A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159129049 | ||||||
| chr4:159129397
|
T | A | 1 | a0001c0001t0002g0096 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.69+25166T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159129397 | ||||||
| chr4:159129409
|
G | A | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+25178G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159129409 | ||||||
| chr4:159129564
|
C | T | 1 | a0001c0002t0001g0018 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.69+25333C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159129564 | ||||||
| chr4:159129780
|
C | T | 40 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.69+25549C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159129780 | ||||||
| chr4:159129833
|
G | A | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.69+25602G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159129833 | ||||||
| chr4:159129887
|
C | T | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+25656C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159129887 | ||||||
| chr4:159130101
|
G | T | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+25870G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159130101 | ||||||
| chr4:159130125
|
C | A | 1 | a0001c0001t0006g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.69+25894C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159130125 | ||||||
| chr4:159130293
|
AC | A | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+26064delC | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159130293 | |||||
| chr4:159130313
|
A | T | 1 | a0001c0003t0004g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.69+26082A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159130313 | ||||||
| chr4:159130465
|
G | A | 1 | a0001c0002t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.69+26234G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159130465 | ||||||
| chr4:159130491
|
G | C | 7 | a0001c0001t0031g0116a0001c0001t0033g0113a0001c0001t0034g0115others(4): Show | 7 | HG01081.hp2 HG01884.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+26260G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159130491 | ||||||
| chr4:159130507
|
G | A | 1 | a0001c0001t0002g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.69+26276G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159130507 | ||||||
| chr4:159130556
|
T | G | 1 | a0001c0004t0003g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.69+26325T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159130556 | ||||||
| chr4:159130571
|
G | A | 1 | a0001c0001t0011g0021 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.69+26340G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159130571 | ||||||
| chr4:159130671
|
C | T | 1 | a0001c0002t0001g0126 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.69+26440C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159130671 | ||||||
| chr4:159130937
|
C | T | 9 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+26706C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159130937 | ||||||
| chr4:159131095
|
TGTGAGAG others(1): Show |
T | 2 | a0001c0001t0002g0015a0001c0002t0001g0034 | 2 | HG00738.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.69+26866_69+26873d others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159131095 | |||||
| chr4:159131097
|
TGA | T | 37 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0171others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.69+26899_69+26900d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159131097 | |||||
| chr4:159131097
|
TGAGA | T | 7 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+26897_69+26900d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159131097 | |||||
| chr4:159131097
|
TGAGAGA | T | 13 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0002g0091others(10): Show | 13 | HG00733.hp2 HG01071.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.69+26895_69+26900d others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159131097 | |||||
| chr4:159131097
|
TGAGAGAG others(1): Show |
T | 123 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0025others(120): Show | 123 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.69+26893_69+26900d others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159131097 | |||||
| chr4:159131097
|
TGAGAGAG others(3): Show |
T | 5 | a0001c0001t0002g0005a0001c0001t0011g0021a0001c0001t0011g0022others(2): Show | 5 | HG02280.hp2 HG02970.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.69+26891_69+26900d others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159131097 | |||||
| chr4:159131099
|
A | T | 3 | a0001c0002t0003g0188a0001c0002t0003g0189a0001c0002t0003g0192 | 3 | HG01361.hp1 HG01978.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.69+26868A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131099 | ||||||
| chr4:159131101
|
A | T | 37 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0171others(34): Show | 37 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.69+26870A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131101 | ||||||
| chr4:159131103
|
A | T | 7 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+26872A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131103 | ||||||
| chr4:159131105
|
A | T | 2 | a0001c0001t0002g0074a0001c0001t0005g0086 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.69+26874A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131105 | ||||||
| chr4:159131107
|
A | T | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.69+26876A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131107 | ||||||
| chr4:159131109
|
A | T | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+26878A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131109 | ||||||
| chr4:159131111
|
A | T | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+26880A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131111 | ||||||
| chr4:159131166
|
A | G | 1 | a0001c0001t0007g0078 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.69+26935A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131166 | ||||||
| chr4:159131196
|
C | T | 4 | a0001c0002t0001g0075a0001c0002t0001g0153a0001c0002t0001g0158others(1): Show | 4 | HG00597.hp1 HG01516.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+26965C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131196 | ||||||
| chr4:159131213
|
C | T | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.69+26982C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131213 | ||||||
| chr4:159131401
|
C | T | 2 | a0001c0001t0005g0092a0001c0001t0005g0093 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.69+27170C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131401 | ||||||
| chr4:159131469
|
T | C | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+27238T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131469 | ||||||
| chr4:159131507
|
T | A | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.69+27276T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131507 | ||||||
| chr4:159131519
|
A | AT | 9 | a0001c0001t0002g0089a0001c0001t0002g0091a0001c0001t0002g0096others(6): Show | 9 | HG00558.hp1 HG00642.hp1 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.69+27315dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159131519 | |||||
| chr4:159131519
|
A | ATTG | 29 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(26): Show | 29 | HG00597.hp2 HG01081.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.69+27290_69+27291i others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159131519 | |||||
| chr4:159131519
|
A | ATTGG | 8 | a0001c0001t0004g0194a0001c0001t0007g0095a0001c0001t0009g0035others(5): Show | 8 | HG00597.hp1 HG01123.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+27290_69+27291i others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159131519 | |||||
| chr4:159131519
|
A | ATTGT | 14 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(11): Show | 14 | HG00099.hp1 HG00280.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.69+27290_69+27291i others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159131519 | |||||
| chr4:159131519
|
AT | A | 7 | a0001c0001t0011g0021a0001c0001t0031g0116a0001c0001t0033g0113others(4): Show | 7 | HG01099.hp1 HG01884.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+27315delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159131519 | |||||
| chr4:159131520
|
T | TTGG | 41 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0025others(38): Show | 41 | HG00438.hp2 HG00738.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.69+27290_69+27291i others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159131520 | |||||
| chr4:159131521
|
T | TG | 2 | a0001c0001t0005g0051a0001c0003t0019g0135 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.69+27290_69+27291i others(3): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131521 | ||||||
| chr4:159131521
|
T | TGG | 39 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0029others(36): Show | 39 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.69+27290_69+27291i others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131521 | ||||||
| chr4:159131522
|
T | G | 4 | a0001c0001t0005g0051a0001c0001t0011g0022a0001c0001t0011g0023others(1): Show | 4 | HG02818.hp2 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+27291T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131522 | ||||||
| chr4:159131523
|
T | G | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+27292T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131523 | ||||||
| chr4:159131524
|
T | G | 1 | a0001c0001t0011g0021 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.69+27293T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131524 | ||||||
| chr4:159131547
|
A | T | 1 | a0001c0002t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.69+27316A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131547 | ||||||
| chr4:159131549
|
C | G | 1 | a0001c0002t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.69+27318C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131549 | ||||||
| chr4:159131654
|
GA | G | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+27425delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159131654 | |||||
| chr4:159131686
|
A | G | 12 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(9): Show | 12 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.69+27455A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159131686 | ||||||
| chr4:159132035
|
C | T | 142 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.69+27804C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159132035 | ||||||
| chr4:159132499
|
G | A | 135 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.69+28268G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159132499 | ||||||
| chr4:159132565
|
C | T | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+28334C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159132565 | ||||||
| chr4:159132660
|
C | G | 6 | a0001c0001t0007g0078a0001c0001t0007g0082a0001c0001t0007g0094others(3): Show | 6 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+28429C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159132660 | ||||||
| chr4:159132660
|
C | T | 1 | a0001c0001t0007g0077 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.69+28429C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159132660 | ||||||
| chr4:159132791
|
T | C | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+28560T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159132791 | ||||||
| chr4:159132882
|
G | GT | 12 | a0001c0001t0002g0090a0001c0001t0002g0101a0001c0001t0007g0077others(9): Show | 12 | HG00438.hp1 HG01123.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.69+28664dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159132882 | |||||
| chr4:159133303
|
A | C | 3 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085 | 3 | HG02559.hp2 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.69+29072A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159133303 | ||||||
| chr4:159133318
|
C | G | 28 | a0001c0001t0002g0001a0001c0001t0002g0025a0001c0001t0002g0060others(25): Show | 28 | HG00438.hp2 HG00597.hp1 HG01516.hp1 others(25): Show |
intron_variant | MODIFIER | c.69+29087C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159133318 | ||||||
| chr4:159133419
|
A | AT | 11 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(8): Show | 11 | HG01123.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.69+29202dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159133419 | |||||
| chr4:159133477
|
T | C | 1 | a0001c0001t0002g0060 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.69+29246T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159133477 | ||||||
| chr4:159133567
|
AC | A | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+29337delC | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159133567 | ||||||
| chr4:159133571
|
G | A | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+29340G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159133571 | ||||||
| chr4:159133637
|
G | A | 1 | a0001c0001t0006g0183 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.69+29406G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159133637 | ||||||
| chr4:159133732
|
T | C | 142 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.69+29501T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159133732 | ||||||
| chr4:159133748
|
T | C | 1 | a0001c0001t0002g0001 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.69+29517T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159133748 | ||||||
| chr4:159133834
|
C | T | 1 | a0001c0002t0003g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.69+29603C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159133834 | ||||||
| chr4:159133848
|
C | T | 2 | a0001c0001t0029g0002a0001c0002t0003g0008 | 2 | HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.69+29617C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159133848 | ||||||
| chr4:159133884
|
A | G | 82 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(79): Show | 82 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.69+29653A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159133884 | ||||||
| chr4:159133906
|
A | T | 2 | a0001c0001t0005g0092a0001c0001t0005g0093 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.69+29675A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159133906 | ||||||
| chr4:159133966
|
G | A | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+29735G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159133966 | ||||||
| chr4:159134024
|
G | A | 9 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+29793G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159134024 | ||||||
| chr4:159134056
|
A | G | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+29825A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159134056 | ||||||
| chr4:159134113
|
C | G | 1 | a0001c0003t0004g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.69+29882C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159134113 | ||||||
| chr4:159134143
|
G | A | 1 | a0001c0001t0007g0078 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.69+29912G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159134143 | ||||||
| chr4:159134188
|
A | G | 1 | a0001c0002t0001g0017 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.69+29957A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159134188 | ||||||
| chr4:159134496
|
A | G | 2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.69+30265A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159134496 | ||||||
| chr4:159134591
|
G | A | 14 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(11): Show | 14 | HG00735.hp1 HG01123.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.69+30360G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159134591 | ||||||
| chr4:159134645
|
C | T | 1 | a0001c0002t0001g0157 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.69+30414C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159134645 | ||||||
| chr4:159134666
|
C | T | 3 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0003g0186 | 3 | HG01516.hp2 HG01517.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.69+30435C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159134666 | ||||||
| chr4:159135054
|
T | C | 12 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(9): Show | 12 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.69+30823T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159135054 | ||||||
| chr4:159135067
|
G | A | 12 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(9): Show | 12 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.69+30836G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159135067 | ||||||
| chr4:159135068
|
G | A | 1 | a0001c0002t0030g0137 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.69+30837G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159135068 | ||||||
| chr4:159135079
|
C | T | 4 | a0001c0002t0003g0172a0001c0002t0003g0178a0001c0002t0003g0179others(1): Show | 4 | HG02717.hp2 HG02723.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+30848C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159135079 | ||||||
| chr4:159135184
|
T | C | 1 | a0001c0001t0006g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.69+30953T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159135184 | ||||||
| chr4:159135216
|
A | G | 191 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.69+30985A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159135216 | ||||||
| chr4:159135260
|
C | T | 1 | a0001c0002t0001g0157 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.69+31029C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159135260 | ||||||
| chr4:159135294
|
C | T | 5 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+31063C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159135294 | ||||||
| chr4:159135334
|
T | C | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+31103T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159135334 | ||||||
| chr4:159135397
|
A | G | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+31166A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159135397 | ||||||
| chr4:159135687
|
C | T | 1 | a0001c0002t0003g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.69+31456C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159135687 | ||||||
| chr4:159135702
|
C | T | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+31471C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159135702 | ||||||
| chr4:159135922
|
T | C | 48 | a0001c0001t0002g0088a0001c0001t0002g0097a0001c0001t0006g0161others(45): Show | 48 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.69+31691T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159135922 | ||||||
| chr4:159135944
|
C | G | 1 | a0001c0002t0001g0039 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.69+31713C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159135944 | ||||||
| chr4:159135956
|
G | A | 1 | a0001c0002t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.69+31725G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159135956 | ||||||
| chr4:159136005
|
A | AT | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+31777dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159136005 | |||||
| chr4:159136061
|
C | A | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+31830C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159136061 | ||||||
| chr4:159136153
|
A | T | 12 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(9): Show | 12 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.69+31922A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159136153 | ||||||
| chr4:159136585
|
A | G | 1 | a0001c0002t0001g0004 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.69+32354A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159136585 | ||||||
| chr4:159136814
|
G | T | 40 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.69+32583G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159136814 | ||||||
| chr4:159136981
|
G | A | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+32750G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159136981 | ||||||
| chr4:159137482
|
C | T | 1 | a0001c0001t0006g0187 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.69+33251C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159137482 | ||||||
| chr4:159137709
|
C | CA | 32 | a0001c0001t0002g0091a0001c0001t0002g0118a0001c0001t0002g0145others(29): Show | 32 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.69+33495dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159137709 | |||||
| chr4:159137709
|
C | CAA | 100 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0029others(97): Show | 100 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.69+33494_69+33495d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159137709 | |||||
| chr4:159137709
|
C | CAAA | 24 | a0001c0001t0002g0015a0001c0001t0002g0044a0001c0001t0002g0057others(21): Show | 24 | HG00099.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.69+33493_69+33495d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159137709 | |||||
| chr4:159137709
|
CA | C | 5 | a0001c0001t0031g0116a0001c0001t0033g0113a0001c0001t0034g0115others(2): Show | 5 | HG01884.hp1 HG02922.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+33495delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159137709 | |||||
| chr4:159138081
|
T | C | 1 | a0001c0001t0008g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.69+33850T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159138081 | ||||||
| chr4:159138187
|
C | T | 3 | a0001c0002t0001g0027a0001c0002t0001g0038a0001c0002t0001g0039 | 3 | HG01069.hp2 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.69+33956C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159138187 | ||||||
| chr4:159138231
|
A | C | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+34000A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159138231 | ||||||
| chr4:159138259
|
G | A | 3 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0003g0186 | 3 | HG01516.hp2 HG01517.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.69+34028G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159138259 | ||||||
| chr4:159138292
|
A | G | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+34061A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159138292 | ||||||
| chr4:159138327
|
A | C | 2 | a0001c0001t0005g0092a0001c0001t0005g0093 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.69+34096A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159138327 | ||||||
| chr4:159138366
|
C | G | 1 | a0001c0001t0002g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.69+34135C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159138366 | ||||||
| chr4:159138474
|
G | A | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+34243G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159138474 | ||||||
| chr4:159138553
|
A | G | 43 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(40): Show | 43 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.69+34322A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159138553 | ||||||
| chr4:159138601
|
T | C | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+34370T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159138601 | ||||||
| chr4:159138608
|
T | C | 1 | a0001c0003t0017g0117 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.69+34377T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159138608 | ||||||
| chr4:159138958
|
G | T | 2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.69+34727G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159138958 | ||||||
| chr4:159139010
|
G | A | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+34779G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159139010 | ||||||
| chr4:159139132
|
C | T | 1 | a0001c0001t0005g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.69+34901C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159139132 | ||||||
| chr4:159139195
|
A | G | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+34964A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159139195 | ||||||
| chr4:159139267
|
G | T | 143 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.69+35036G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159139267 | ||||||
| chr4:159139279
|
GA | G | 4 | a0001c0002t0001g0075a0001c0002t0001g0153a0001c0002t0001g0158others(1): Show | 4 | HG00597.hp1 HG01516.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+35052delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159139279 | |||||
| chr4:159139312
|
C | G | 5 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+35081C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159139312 | ||||||
| chr4:159139334
|
G | A | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+35103G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159139334 | ||||||
| chr4:159139339
|
C | T | 77 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(74): Show | 77 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.69+35108C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159139339 | ||||||
| chr4:159139446
|
A | G | 2 | a0001c0001t0027g0104a0001c0002t0003g0136 | 2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.69+35215A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159139446 | ||||||
| chr4:159139573
|
A | AT | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+35344dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159139573 | |||||
| chr4:159139842
|
G | A | 21 | a0001c0001t0002g0005a0001c0001t0002g0057a0001c0001t0002g0074others(18): Show | 21 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.69+35611G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159139842 | ||||||
| chr4:159139863
|
G | T | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+35632G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159139863 | ||||||
| chr4:159139888
|
A | G | 1 | a0001c0002t0001g0138 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.69+35657A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159139888 | ||||||
| chr4:159139890
|
G | T | 21 | a0001c0001t0002g0005a0001c0001t0002g0057a0001c0001t0002g0074others(18): Show | 21 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.69+35659G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159139890 | ||||||
| chr4:159139947
|
A | G | 3 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085 | 3 | HG02559.hp2 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.69+35716A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159139947 | ||||||
| chr4:159140006
|
C | T | 2 | a0001c0002t0003g0150a0001c0002t0003g0182 | 2 | HG01261.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.69+35775C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159140006 | ||||||
| chr4:159140043
|
G | C | 1 | a0001c0003t0004g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.69+35812G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159140043 | ||||||
| chr4:159140175
|
C | T | 7 | a0001c0001t0006g0161a0001c0001t0006g0171a0001c0001t0006g0175others(4): Show | 7 | HG00597.hp2 HG01099.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+35944C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159140175 | ||||||
| chr4:159140212
|
T | C | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+35981T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159140212 | ||||||
| chr4:159140268
|
A | G | 3 | a0001c0001t0009g0035a0001c0001t0029g0002a0001c0002t0003g0008 | 3 | HG02055.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.69+36037A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159140268 | ||||||
| chr4:159140592
|
G | A | 1 | a0001c0001t0006g0177 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.69+36361G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159140592 | ||||||
| chr4:159140685
|
A | G | 10 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(7): Show | 10 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+36454A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159140685 | ||||||
| chr4:159140728
|
G | A | 10 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(7): Show | 10 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+36497G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159140728 | ||||||
| chr4:159140803
|
T | C | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+36572T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159140803 | ||||||
| chr4:159140824
|
G | GA | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG00639.hp2 HG00738.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+36606dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159140824 | |||||
| chr4:159140824
|
GA | G | 121 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.69+36606delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159140824 | |||||
| chr4:159141259
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.69+37028A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159141259 | ||||||
| chr4:159141298
|
G | A | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+37067G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159141298 | ||||||
| chr4:159141358
|
C | T | 1 | a0001c0002t0003g0150 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.69+37127C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159141358 | ||||||
| chr4:159141436
|
T | G | 10 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(7): Show | 10 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+37205T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159141436 | ||||||
| chr4:159141441
|
T | A | 10 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(7): Show | 10 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+37210T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159141441 | ||||||
| chr4:159141544
|
C | A | 10 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(7): Show | 10 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+37313C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159141544 | ||||||
| chr4:159141591
|
T | C | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+37360T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159141591 | ||||||
| chr4:159141594
|
A | ATG | 26 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0029others(23): Show | 26 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.69+37364_69+37365i others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159141594 | |||||
| chr4:159141652
|
T | C | 42 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(39): Show | 42 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.69+37421T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159141652 | ||||||
| chr4:159141673
|
C | G | 2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.69+37442C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159141673 | ||||||
| chr4:159141689
|
G | A | 1 | a0001c0004t0003g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.69+37458G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159141689 | ||||||
| chr4:159141704
|
G | A | 72 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(69): Show | 72 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.69+37473G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159141704 | ||||||
| chr4:159142313
|
G | A | 42 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(39): Show | 42 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.69+38082G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159142313 | ||||||
| chr4:159142451
|
A | G | 4 | a0001c0001t0004g0193a0001c0001t0005g0092a0001c0001t0005g0093others(1): Show | 4 | NA18906.hp2 NA19043.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+38220A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159142451 | ||||||
| chr4:159142513
|
G | T | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+38282G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159142513 | ||||||
| chr4:159142513
|
GT | G | 11 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(8): Show | 11 | HG01081.hp2 HG01109.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.69+38295delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159142513 | |||||
| chr4:159142528
|
T | C | 1 | a0001c0002t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.69+38297T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159142528 | ||||||
| chr4:159142616
|
A | C | 1 | a0001c0002t0001g0007 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.69+38385A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159142616 | ||||||
| chr4:159142720
|
T | A | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+38489T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159142720 | ||||||
| chr4:159142738
|
A | C | 2 | a0001c0002t0003g0160a0001c0002t0003g0166 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.69+38507A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159142738 | ||||||
| chr4:159142794
|
G | A | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.69+38563G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159142794 | ||||||
| chr4:159142970
|
C | T | 1 | a0001c0001t0006g0163 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.69+38739C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159142970 | ||||||
| chr4:159143072
|
G | T | 1 | a0001c0002t0003g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.69+38841G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159143072 | ||||||
| chr4:159143121
|
C | T | 77 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(74): Show | 77 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.69+38890C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159143121 | ||||||
| chr4:159143167
|
C | T | 1 | a0001c0002t0003g0173 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.69+38936C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159143167 | ||||||
| chr4:159143275
|
C | A | 1 | a0001c0001t0002g0154 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.69+39044C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159143275 | ||||||
| chr4:159143275
|
C | CA | 4 | a0001c0001t0002g0060a0001c0001t0005g0086a0001c0001t0020g0120others(1): Show | 4 | HG00438.hp2 HG02109.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.69+39051dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159143275 | |||||
| chr4:159143289
|
A | C | 2 | a0001c0001t0027g0104a0001c0002t0003g0136 | 2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.69+39058A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159143289 | ||||||
| chr4:159143295
|
T | A | 1 | a0001c0002t0003g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.69+39064T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159143295 | ||||||
| chr4:159143362
|
A | G | 22 | a0001c0001t0002g0005a0001c0001t0002g0057a0001c0001t0002g0074others(19): Show | 22 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.69+39131A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159143362 | ||||||
| chr4:159143499
|
G | A | 10 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(7): Show | 10 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+39268G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159143499 | ||||||
| chr4:159143519
|
A | G | 1 | a0001c0002t0001g0158 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.69+39288A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159143519 | ||||||
| chr4:159143530
|
A | T | 1 | a0001c0002t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.69+39299A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159143530 | ||||||
| chr4:159143654
|
G | C | 1 | a0001c0004t0003g0159 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.69+39423G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159143654 | ||||||
| chr4:159143750
|
A | G | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.69+39519A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159143750 | ||||||
| chr4:159143810
|
G | C | 1 | a0001c0001t0004g0193 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.69+39579G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159143810 | ||||||
| chr4:159143896
|
G | A | 1 | a0001c0001t0007g0077 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.69+39665G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159143896 | ||||||
| chr4:159143907
|
A | T | 10 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(7): Show | 10 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+39676A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159143907 | ||||||
| chr4:159143943
|
A | T | 10 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(7): Show | 10 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+39712A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159143943 | ||||||
| chr4:159144179
|
C | T | 2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.69+39948C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159144179 | ||||||
| chr4:159144182
|
A | ATTTAATA others(9): Show |
2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.69+39951_69+39952i others(18): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159144182 | ||||||
| chr4:159144211
|
G | A | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.69+39980G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159144211 | ||||||
| chr4:159144223
|
C | G | 1 | a0001c0001t0002g0089 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.69+39992C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159144223 | ||||||
| chr4:159144243
|
A | C | 77 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(74): Show | 77 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.69+40012A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159144243 | ||||||
| chr4:159144588
|
C | G | 1 | a0001c0002t0003g0181 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.69+40357C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159144588 | ||||||
| chr4:159144608
|
A | ATGTTTAC others(2): Show |
10 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(7): Show | 10 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+40382_69+40390d others(11): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159144608 | |||||
| chr4:159144863
|
T | C | 11 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(8): Show | 11 | HG02280.hp2 HG02559.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.69+40632T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159144863 | ||||||
| chr4:159144879
|
G | GTTTT | 23 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(20): Show | 23 | HG00099.hp1 HG00280.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.69+40671_69+40674d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159144879 | |||||
| chr4:159144879
|
G | GTTTTT | 11 | a0001c0001t0006g0175a0001c0001t0010g0165a0001c0001t0015g0190others(8): Show | 11 | HG01123.hp2 HG01261.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.69+40670_69+40674d others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159144879 | |||||
| chr4:159144879
|
G | GTTTTTTT others(4): Show |
1 | a0001c0003t0017g0117 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.69+40664_69+40674d others(13): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159144879 | |||||
| chr4:159144879
|
G | GTTTTTTT others(5): Show |
1 | a0001c0002t0003g0166 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.69+40663_69+40674d others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159144879 | |||||
| chr4:159144879
|
GTT | G | 6 | a0001c0001t0002g0076a0001c0001t0002g0109a0001c0001t0002g0121others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+40673_69+40674d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159144879 | |||||
| chr4:159144879
|
GTTT | G | 46 | a0001c0001t0002g0005a0001c0001t0002g0079a0001c0001t0002g0088others(43): Show | 46 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.69+40672_69+40674d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159144879 | |||||
| chr4:159144879
|
GTTTTT | G | 6 | a0001c0001t0007g0078a0001c0001t0007g0082a0001c0001t0007g0094others(3): Show | 6 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.69+40670_69+40674d others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159144879 | |||||
| chr4:159144879
|
GTTTTTTT others(3): Show |
G | 73 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(70): Show | 73 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.69+40665_69+40674d others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159144879 | |||||
| chr4:159144947
|
G | T | 18 | a0001c0001t0002g0001a0001c0001t0002g0025a0001c0001t0002g0060others(15): Show | 18 | HG00438.hp2 HG02074.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.69+40716G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159144947 | ||||||
| chr4:159145165
|
G | A | 1 | a0001c0002t0001g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.69+40934G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159145165 | ||||||
| chr4:159145194
|
C | T | 1 | a0001c0001t0002g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.69+40963C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159145194 | ||||||
| chr4:159145469
|
C | G | 1 | a0001c0002t0001g0158 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.70-41173C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159145469 | ||||||
| chr4:159145482
|
C | CAAAACAT others(5): Show |
4 | a0001c0002t0001g0075a0001c0002t0001g0153a0001c0002t0001g0158others(1): Show | 4 | HG00597.hp1 HG01516.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-41139_70-41128d others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159145482 | |||||
| chr4:159145620
|
G | A | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.70-41022G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159145620 | ||||||
| chr4:159145721
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.70-40921G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159145721 | ||||||
| chr4:159145821
|
G | A | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-40821G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159145821 | ||||||
| chr4:159145955
|
C | A | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.70-40687C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159145955 | ||||||
| chr4:159145955
|
C | T | 1 | a0001c0001t0013g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.70-40687C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159145955 | ||||||
| chr4:159145956
|
G | A | 1 | a0001c0002t0001g0013 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.70-40686G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159145956 | ||||||
| chr4:159145996
|
G | A | 37 | a0001c0001t0002g0079a0001c0001t0002g0088a0001c0001t0002g0089others(34): Show | 37 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.70-40646G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159145996 | ||||||
| chr4:159146231
|
G | A | 135 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.70-40411G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159146231 | ||||||
| chr4:159146361
|
CT | C | 10 | a0001c0002t0001g0013a0001c0003t0004g0009a0001c0003t0004g0047others(7): Show | 10 | HG01167.hp2 HG01258.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.70-40268delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159146361 | |||||
| chr4:159146444
|
T | G | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.70-40198T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159146444 | ||||||
| chr4:159146550
|
G | C | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70-40092G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159146550 | ||||||
| chr4:159146552
|
A | G | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70-40090A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159146552 | ||||||
| chr4:159146589
|
A | T | 5 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-40053A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159146589 | ||||||
| chr4:159146766
|
C | T | 1 | a0001c0002t0003g0173 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.70-39876C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159146766 | ||||||
| chr4:159146929
|
A | G | 1 | a0001c0001t0005g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.70-39713A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159146929 | ||||||
| chr4:159146930
|
C | T | 38 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0029others(35): Show | 38 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.70-39712C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159146930 | ||||||
| chr4:159146976
|
G | A | 2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.70-39666G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159146976 | ||||||
| chr4:159147073
|
C | T | 3 | a0001c0001t0009g0035a0001c0001t0029g0002a0001c0002t0003g0008 | 3 | HG02055.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.70-39569C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159147073 | ||||||
| chr4:159147121
|
G | A | 2 | a0001c0001t0008g0033a0001c0001t0008g0041 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.70-39521G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159147121 | ||||||
| chr4:159147227
|
A | G | 12 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(9): Show | 12 | HG02280.hp2 HG02559.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.70-39415A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159147227 | ||||||
| chr4:159147284
|
G | A | 2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.70-39358G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159147284 | ||||||
| chr4:159147291
|
C | T | 1 | a0001c0002t0001g0158 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.70-39351C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159147291 | ||||||
| chr4:159147363
|
CA | C | 10 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(7): Show | 10 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-39274delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159147363 | |||||
| chr4:159147372
|
C | CT | 11 | a0001c0001t0002g0005a0001c0001t0002g0101a0001c0001t0007g0077others(8): Show | 11 | HG00438.hp1 HG01081.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.70-39259dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159147372 | |||||
| chr4:159147384
|
G | T | 38 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0029others(35): Show | 38 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.70-39258G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159147384 | ||||||
| chr4:159147486
|
T | C | 2 | a0001c0001t0008g0070a0001c0002t0001g0050 | 2 | HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.70-39156T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159147486 | ||||||
| chr4:159147570
|
T | A | 1 | a0001c0001t0002g0118 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.70-39072T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159147570 | ||||||
| chr4:159147854
|
CA | C | 4 | a0001c0001t0004g0193a0001c0001t0005g0092a0001c0001t0005g0093others(1): Show | 4 | NA18906.hp2 NA19043.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-38787delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159147854 | ||||||
| chr4:159147921
|
T | G | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-38721T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159147921 | ||||||
| chr4:159147925
|
T | C | 27 | a0001c0001t0002g0001a0001c0001t0002g0025a0001c0001t0002g0060others(24): Show | 27 | HG00438.hp2 HG00597.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.70-38717T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159147925 | ||||||
| chr4:159148147
|
A | G | 143 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.70-38495A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159148147 | ||||||
| chr4:159148272
|
C | T | 10 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(7): Show | 10 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-38370C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159148272 | ||||||
| chr4:159148300
|
A | G | 1 | a0001c0001t0002g0057 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.70-38342A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159148300 | ||||||
| chr4:159148335
|
T | G | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.70-38307T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159148335 | ||||||
| chr4:159148368
|
T | A | 2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.70-38274T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159148368 | ||||||
| chr4:159148524
|
G | A | 1 | a0001c0004t0001g0020 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.70-38118G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159148524 | ||||||
| chr4:159148564
|
G | T | 1 | a0001c0001t0033g0113 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.70-38078G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159148564 | ||||||
| chr4:159148860
|
T | C | 2 | a0001c0001t0027g0104a0001c0002t0003g0136 | 2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.70-37782T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159148860 | ||||||
| chr4:159148889
|
A | T | 185 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(182): Show | 185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.70-37753A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159148889 | ||||||
| chr4:159149035
|
G | A | 6 | a0001c0001t0031g0116a0001c0001t0033g0113a0001c0001t0034g0115others(3): Show | 6 | HG01884.hp1 HG02257.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-37607G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159149035 | ||||||
| chr4:159149378
|
C | T | 17 | a0001c0001t0002g0029a0001c0002t0001g0006a0001c0002t0001g0007others(14): Show | 17 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.70-37264C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159149378 | ||||||
| chr4:159149399
|
C | T | 133 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.70-37243C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159149399 | ||||||
| chr4:159149545
|
C | G | 133 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.70-37097C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159149545 | ||||||
| chr4:159149574
|
T | C | 2 | a0001c0002t0001g0014a0001c0002t0001g0042 | 2 | HG01496.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.70-37068T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159149574 | ||||||
| chr4:159149935
|
G | A | 4 | a0001c0002t0001g0075a0001c0002t0001g0153a0001c0002t0001g0158others(1): Show | 4 | HG00597.hp1 HG01516.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-36707G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159149935 | ||||||
| chr4:159150009
|
TTC | T | 72 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(69): Show | 72 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.70-36631_70-36630d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159150009 | |||||
| chr4:159150094
|
ATTAATTT others(64): Show |
A | 12 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(9): Show | 12 | HG02280.hp2 HG02559.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.70-36512_70-36442d others(73): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159150094 | |||||
| chr4:159150137
|
C | T | 123 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(120): Show | 123 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.70-36505C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159150137 | ||||||
| chr4:159150150
|
T | C | 1 | a0001c0003t0017g0117 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.70-36492T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159150150 | ||||||
| chr4:159150200
|
A | T | 121 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.70-36442A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159150200 | ||||||
| chr4:159150202
|
G | T | 121 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.70-36440G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159150202 | ||||||
| chr4:159150254
|
C | A | 1 | a0001c0001t0024g0087 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.70-36388C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159150254 | ||||||
| chr4:159150254
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.70-36388C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159150254 | ||||||
| chr4:159150602
|
A | G | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.70-36040A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159150602 | ||||||
| chr4:159150773
|
G | A | 121 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.70-35869G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159150773 | ||||||
| chr4:159150991
|
G | A | 9 | a0001c0001t0006g0183a0001c0001t0006g0184a0001c0002t0001g0133others(6): Show | 9 | HG00099.hp1 HG01106.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.70-35651G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159150991 | ||||||
| chr4:159151074
|
T | C | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-35568T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159151074 | ||||||
| chr4:159151086
|
T | C | 2 | a0001c0001t0033g0113a0001c0001t0034g0115 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.70-35556T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159151086 | ||||||
| chr4:159151283
|
A | G | 143 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.70-35359A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159151283 | ||||||
| chr4:159151390
|
C | T | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.70-35252C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159151390 | ||||||
| chr4:159151499
|
C | T | 40 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.70-35143C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159151499 | ||||||
| chr4:159151600
|
CTGATACA others(3): Show |
C | 2 | a0001c0001t0002g0015a0001c0002t0001g0034 | 2 | HG00738.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.70-35039_70-35030d others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159151600 | |||||
| chr4:159151780
|
G | A | 4 | a0001c0001t0004g0193a0001c0001t0005g0092a0001c0001t0005g0093others(1): Show | 4 | NA18906.hp2 NA19043.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-34862G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159151780 | ||||||
| chr4:159152186
|
G | GTGT | 7 | a0001c0001t0002g0066a0001c0001t0008g0062a0001c0001t0008g0067others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-34453_70-34451d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159152186 | |||||
| chr4:159152210
|
G | A | 133 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.70-34432G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159152210 | ||||||
| chr4:159152224
|
G | A | 1 | a0001c0001t0002g0124 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.70-34418G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159152224 | ||||||
| chr4:159152319
|
TA | T | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-34314delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159152319 | |||||
| chr4:159152387
|
T | C | 135 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.70-34255T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159152387 | ||||||
| chr4:159152399
|
C | G | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.70-34243C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159152399 | ||||||
| chr4:159152524
|
G | C | 1 | a0001c0001t0002g0057 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.70-34118G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159152524 | ||||||
| chr4:159152718
|
C | T | 2 | a0001c0002t0001g0018a0001c0002t0003g0186 | 2 | HG02559.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.70-33924C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159152718 | ||||||
| chr4:159152774
|
C | T | 1 | a0001c0002t0003g0176 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.70-33868C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159152774 | ||||||
| chr4:159152775
|
G | A | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70-33867G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159152775 | ||||||
| chr4:159152821
|
G | A | 11 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(8): Show | 11 | HG02280.hp2 HG02559.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.70-33821G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159152821 | ||||||
| chr4:159152862
|
G | A | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.70-33780G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159152862 | ||||||
| chr4:159152867
|
C | T | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.70-33775C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159152867 | ||||||
| chr4:159152906
|
G | A | 44 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(41): Show | 44 | HG00099.hp2 HG00438.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.70-33736G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159152906 | ||||||
| chr4:159153010
|
G | A | 12 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(9): Show | 12 | HG02280.hp2 HG02559.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.70-33632G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159153010 | ||||||
| chr4:159153092
|
A | C | 1 | a0001c0001t0002g0015 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.70-33550A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159153092 | ||||||
| chr4:159153120
|
T | A | 1 | a0001c0003t0017g0117 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.70-33522T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159153120 | ||||||
| chr4:159153223
|
G | A | 1 | a0001c0002t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.70-33419G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159153223 | ||||||
| chr4:159153496
|
C | T | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.70-33146C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159153496 | ||||||
| chr4:159153543
|
C | T | 1 | a0001c0001t0002g0015 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.70-33099C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159153543 | ||||||
| chr4:159153693
|
T | C | 22 | a0001c0001t0002g0005a0001c0001t0002g0057a0001c0001t0002g0074others(19): Show | 22 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.70-32949T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159153693 | ||||||
| chr4:159153998
|
A | G | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.70-32644A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159153998 | ||||||
| chr4:159154224
|
G | T | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.70-32418G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159154224 | ||||||
| chr4:159154282
|
A | G | 1 | a0001c0002t0001g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.70-32360A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159154282 | ||||||
| chr4:159154287
|
A | C | 1 | a0001c0002t0001g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.70-32355A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159154287 | ||||||
| chr4:159154296
|
A | G | 1 | a0001c0003t0004g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.70-32346A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159154296 | ||||||
| chr4:159154505
|
C | CT | 68 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(65): Show | 68 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.70-32123dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159154505 | |||||
| chr4:159154517
|
T | TAA | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.70-32125_70-32124i others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159154517 | ||||||
| chr4:159154518
|
T | A | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.70-32124T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159154518 | ||||||
| chr4:159154518
|
T | TA | 2 | a0001c0001t0002g0057a0001c0003t0017g0117 | 2 | HG01081.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.70-32124_70-32123i others(3): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159154518 | ||||||
| chr4:159154519
|
T | A | 6 | a0001c0001t0002g0057a0001c0001t0011g0021a0001c0001t0011g0022others(3): Show | 6 | HG01081.hp2 HG02280.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-32123T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159154519 | ||||||
| chr4:159154519
|
T | TA | 57 | a0001c0001t0002g0074a0001c0001t0005g0051a0001c0001t0005g0086others(54): Show | 57 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.70-32115dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159154519 | |||||
| chr4:159154528
|
C | A | 4 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(1): Show | 4 | HG02886.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-32114C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159154528 | ||||||
| chr4:159154575
|
T | C | 1 | a0001c0002t0001g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.70-32067T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159154575 | ||||||
| chr4:159154804
|
G | A | 42 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(39): Show | 42 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.70-31838G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159154804 | ||||||
| chr4:159154825
|
T | C | 1 | a0001c0002t0001g0157 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.70-31817T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159154825 | ||||||
| chr4:159154857
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.70-31785A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159154857 | ||||||
| chr4:159154867
|
T | G | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-31775T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159154867 | ||||||
| chr4:159154989
|
C | T | 4 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(1): Show | 4 | HG02886.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-31653C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159154989 | ||||||
| chr4:159155297
|
A | G | 1 | a0001c0001t0002g0010 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.70-31345A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159155297 | ||||||
| chr4:159155532
|
CAGA | C | 143 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(140): Show | 143 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.70-31109_70-31107d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159155532 | ||||||
| chr4:159155545
|
A | G | 1 | a0001c0001t0005g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.70-31097A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159155545 | ||||||
| chr4:159155548
|
G | A | 135 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.70-31094G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159155548 | ||||||
| chr4:159155769
|
CT | C | 40 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0025others(37): Show | 40 | HG00438.hp2 HG00597.hp1 HG01516.hp1 others(37): Show |
intron_variant | MODIFIER | c.70-30860delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159155769 | |||||
| chr4:159155960
|
A | G | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-30682A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159155960 | ||||||
| chr4:159156069
|
G | A | 2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.70-30573G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159156069 | ||||||
| chr4:159156273
|
C | T | 26 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0029others(23): Show | 26 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-30369C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159156273 | ||||||
| chr4:159156530
|
A | G | 1 | a0001c0001t0002g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.70-30112A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159156530 | ||||||
| chr4:159156588
|
A | T | 9 | a0001c0001t0006g0163a0001c0001t0010g0155a0001c0001t0010g0162others(6): Show | 9 | HG01884.hp2 HG01981.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.70-30054A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159156588 | ||||||
| chr4:159156732
|
C | A | 21 | a0001c0001t0002g0005a0001c0001t0002g0057a0001c0001t0002g0074others(18): Show | 21 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.70-29910C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159156732 | ||||||
| chr4:159156891
|
A | G | 1 | a0001c0001t0002g0089 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.70-29751A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159156891 | ||||||
| chr4:159157033
|
A | C | 2 | a0001c0001t0027g0104a0001c0002t0003g0136 | 2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.70-29609A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159157033 | ||||||
| chr4:159157097
|
G | T | 11 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(8): Show | 11 | HG02280.hp2 HG02559.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.70-29545G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159157097 | ||||||
| chr4:159157108
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.70-29534T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159157108 | ||||||
| chr4:159157248
|
G | A | 1 | a0001c0002t0003g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.70-29394G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159157248 | ||||||
| chr4:159157424
|
T | C | 5 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-29218T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159157424 | ||||||
| chr4:159157472
|
G | A | 1 | a0001c0003t0019g0135 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.70-29170G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159157472 | ||||||
| chr4:159157491
|
T | C | 1 | a0001c0003t0017g0117 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.70-29151T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159157491 | ||||||
| chr4:159157542
|
A | G | 1 | a0001c0002t0003g0176 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.70-29100A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159157542 | ||||||
| chr4:159157620
|
G | A | 2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.70-29022G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159157620 | ||||||
| chr4:159157663
|
G | C | 1 | a0001c0001t0002g0057 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.70-28979G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159157663 | ||||||
| chr4:159157666
|
C | T | 2 | a0001c0001t0002g0121a0001c0001t0020g0120 | 2 | HG02602.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.70-28976C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159157666 | ||||||
| chr4:159157731
|
T | G | 37 | a0001c0001t0002g0079a0001c0001t0002g0088a0001c0001t0002g0089others(34): Show | 37 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.70-28911T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159157731 | ||||||
| chr4:159157740
|
T | C | 4 | a0001c0002t0001g0027a0001c0002t0001g0038a0001c0002t0001g0039others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-28902T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159157740 | ||||||
| chr4:159157947
|
G | A | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-28695G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159157947 | ||||||
| chr4:159158011
|
G | A | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.70-28631G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159158011 | ||||||
| chr4:159158234
|
T | C | 5 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(2): Show | 5 | HG02630.hp1 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-28408T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159158234 | ||||||
| chr4:159158263
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.70-28379C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159158263 | ||||||
| chr4:159158340
|
G | T | 2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.70-28302G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159158340 | ||||||
| chr4:159158672
|
C | G | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.70-27970C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159158672 | ||||||
| chr4:159158786
|
A | G | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-27856A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159158786 | ||||||
| chr4:159158801
|
C | T | 1 | a0001c0002t0001g0075 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.70-27841C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159158801 | ||||||
| chr4:159158809
|
C | A | 35 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0029others(32): Show | 35 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.70-27833C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159158809 | ||||||
| chr4:159158911
|
T | C | 10 | a0001c0001t0002g0071a0001c0001t0009g0058a0001c0001t0009g0059others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-27731T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159158911 | ||||||
| chr4:159158971
|
C | T | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70-27671C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159158971 | ||||||
| chr4:159159079
|
AC | A | 2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.70-27562delC | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159159079 | ||||||
| chr4:159159173
|
G | A | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.70-27469G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159159173 | ||||||
| chr4:159159174
|
C | T | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-27468C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159159174 | ||||||
| chr4:159159346
|
GAGAAAAT others(79): Show |
G | 85 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(82): Show | 85 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.70-27120_70-27035d others(88): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159159346 | |||||
| chr4:159159379
|
T | C | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.70-27263T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159159379 | ||||||
| chr4:159159406
|
A | G | 1 | a0001c0002t0003g0176 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.70-27236A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159159406 | ||||||
| chr4:159159499
|
C | T | 2 | a0001c0001t0002g0025a0001c0001t0005g0049 | 2 | NA18955.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.70-27143C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159159499 | ||||||
| chr4:159159652
|
A | G | 5 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0005g0092others(2): Show | 5 | NA18906.hp2 NA19043.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-26990A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159159652 | ||||||
| chr4:159159718
|
T | G | 45 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(42): Show | 45 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.70-26924T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159159718 | ||||||
| chr4:159159884
|
G | A | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-26758G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159159884 | ||||||
| chr4:159160050
|
C | G | 2 | a0001c0001t0002g0010a0002c0009t0002g0011 | 2 | HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.70-26592C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159160050 | ||||||
| chr4:159160051
|
A | G | 1 | a0001c0001t0002g0130 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.70-26591A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159160051 | ||||||
| chr4:159160422
|
G | A | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-26220G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159160422 | ||||||
| chr4:159160466
|
C | T | 2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.70-26176C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159160466 | ||||||
| chr4:159160598
|
G | A | 1 | a0001c0002t0003g0180 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.70-26044G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159160598 | ||||||
| chr4:159160654
|
T | C | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-25988T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159160654 | ||||||
| chr4:159160984
|
GT | G | 42 | a0001c0001t0002g0079a0001c0001t0002g0088a0001c0001t0002g0089others(39): Show | 42 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.70-25650delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159160984 | |||||
| chr4:159161092
|
C | T | 1 | a0001c0001t0008g0112 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.70-25550C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159161092 | ||||||
| chr4:159161392
|
C | T | 1 | a0001c0001t0015g0191 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.70-25250C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159161392 | ||||||
| chr4:159161420
|
T | C | 4 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(1): Show | 4 | HG02886.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-25222T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159161420 | ||||||
| chr4:159161458
|
A | C | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-25184A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159161458 | ||||||
| chr4:159161504
|
G | C | 2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.70-25138G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159161504 | ||||||
| chr4:159161530
|
C | T | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.70-25112C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159161530 | ||||||
| chr4:159161707
|
G | A | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.70-24935G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159161707 | ||||||
| chr4:159161843
|
G | T | 4 | a0001c0001t0004g0193a0001c0001t0005g0092a0001c0001t0005g0093others(1): Show | 4 | NA18906.hp2 NA19043.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-24799G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159161843 | ||||||
| chr4:159161853
|
C | A | 42 | a0001c0001t0002g0079a0001c0001t0002g0088a0001c0001t0002g0089others(39): Show | 42 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.70-24789C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159161853 | ||||||
| chr4:159161913
|
T | C | 77 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(74): Show | 77 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.70-24729T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159161913 | ||||||
| chr4:159162052
|
A | G | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70-24590A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159162052 | ||||||
| chr4:159162142
|
T | G | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70-24500T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159162142 | ||||||
| chr4:159162221
|
C | CA | 56 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(53): Show | 56 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.70-24401dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159162221 | |||||
| chr4:159162221
|
C | CAA | 26 | a0001c0001t0002g0066a0001c0001t0004g0193a0001c0001t0009g0035others(23): Show | 26 | HG00597.hp1 HG00642.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-24402_70-24401d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159162221 | |||||
| chr4:159162221
|
CAA | C | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-24402_70-24401d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159162221 | |||||
| chr4:159162237
|
A | C | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-24405A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159162237 | ||||||
| chr4:159162362
|
C | T | 1 | a0001c0001t0005g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.70-24280C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159162362 | ||||||
| chr4:159162395
|
TA | T | 7 | a0001c0001t0002g0025a0001c0001t0002g0071a0001c0001t0002g0103others(4): Show | 7 | HG01993.hp1 HG02258.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-24232delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159162395 | |||||
| chr4:159162532
|
A | G | 10 | a0001c0001t0002g0005a0001c0001t0007g0077a0001c0001t0007g0078others(7): Show | 10 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-24110A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159162532 | ||||||
| chr4:159162764
|
A | G | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.70-23878A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159162764 | ||||||
| chr4:159162886
|
A | AT | 11 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(8): Show | 11 | HG02280.hp2 HG02559.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.70-23747dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159162886 | |||||
| chr4:159163020
|
G | T | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.70-23622G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159163020 | ||||||
| chr4:159163040
|
A | T | 2 | a0001c0001t0002g0121a0001c0001t0020g0120 | 2 | HG02602.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.70-23602A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159163040 | ||||||
| chr4:159163230
|
C | T | 1 | a0001c0003t0017g0117 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.70-23412C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159163230 | ||||||
| chr4:159163251
|
A | G | 43 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(40): Show | 43 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.70-23391A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159163251 | ||||||
| chr4:159163348
|
G | A | 1 | a0001c0001t0006g0187 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.70-23294G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159163348 | ||||||
| chr4:159163419
|
G | T | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70-23223G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159163419 | ||||||
| chr4:159163419
|
GT | G | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG00735.hp1 HG01081.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.70-23222delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159163419 | ||||||
| chr4:159163421
|
A | C | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG00735.hp1 HG01081.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.70-23221A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159163421 | ||||||
| chr4:159163520
|
G | A | 21 | a0001c0001t0002g0005a0001c0001t0002g0057a0001c0001t0002g0074others(18): Show | 21 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.70-23122G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159163520 | ||||||
| chr4:159163541
|
T | A | 1 | a0001c0001t0002g0125 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.70-23101T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159163541 | ||||||
| chr4:159163801
|
A | AAG | 23 | a0001c0001t0002g0005a0001c0001t0002g0057a0001c0001t0002g0074others(20): Show | 23 | HG00735.hp1 HG01081.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.70-22840_70-22839d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159163801 | |||||
| chr4:159163844
|
C | T | 1 | a0001c0001t0006g0171 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.70-22798C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159163844 | ||||||
| chr4:159163876
|
A | C | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG00735.hp1 HG01081.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.70-22766A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159163876 | ||||||
| chr4:159163904
|
CTT | C | 17 | a0001c0001t0002g0001a0001c0001t0002g0025a0001c0001t0002g0060others(14): Show | 17 | HG00438.hp2 HG02074.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.70-22737_70-22736d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159163904 | ||||||
| chr4:159164234
|
G | A | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-22408G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159164234 | ||||||
| chr4:159164271
|
T | A | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.70-22371T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159164271 | ||||||
| chr4:159164281
|
G | T | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.70-22361G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159164281 | ||||||
| chr4:159164291
|
A | G | 8 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(5): Show | 8 | HG02559.hp2 HG02647.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.70-22351A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159164291 | ||||||
| chr4:159164299
|
C | T | 4 | a0001c0001t0004g0193a0001c0001t0005g0092a0001c0001t0005g0093others(1): Show | 4 | NA18906.hp2 NA19043.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-22343C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159164299 | ||||||
| chr4:159164304
|
GT | G | 135 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.70-22323delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159164304 | |||||
| chr4:159164534
|
T | C | 41 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.70-22108T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159164534 | ||||||
| chr4:159164727
|
G | A | 191 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.70-21915G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159164727 | ||||||
| chr4:159164804
|
T | C | 2 | a0001c0002t0018g0148a0001c0003t0019g0135 | 2 | HG00735.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.70-21838T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159164804 | ||||||
| chr4:159165280
|
A | T | 1 | a0001c0001t0025g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.70-21362A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159165280 | ||||||
| chr4:159165378
|
T | C | 4 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(1): Show | 4 | HG02886.hp1 HG03041.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-21264T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159165378 | ||||||
| chr4:159165404
|
T | C | 1 | a0001c0001t0002g0101 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.70-21238T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159165404 | ||||||
| chr4:159165443
|
A | G | 1 | a0001c0001t0020g0120 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.70-21199A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159165443 | ||||||
| chr4:159165669
|
G | A | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.70-20973G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159165669 | ||||||
| chr4:159165776
|
A | T | 17 | a0001c0001t0002g0001a0001c0001t0002g0025a0001c0001t0002g0060others(14): Show | 17 | HG00438.hp2 HG02074.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.70-20866A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159165776 | ||||||
| chr4:159165898
|
T | C | 2 | a0001c0001t0005g0092a0001c0001t0005g0093 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.70-20744T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159165898 | ||||||
| chr4:159166142
|
A | G | 142 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(139): Show | 142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.70-20500A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159166142 | ||||||
| chr4:159166334
|
A | T | 41 | a0001c0001t0006g0161a0001c0001t0006g0163a0001c0001t0006g0170others(38): Show | 41 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.70-20308A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159166334 | ||||||
| chr4:159166335
|
G | A | 25 | a0001c0001t0002g0001a0001c0001t0002g0025a0001c0001t0002g0060others(22): Show | 25 | HG00438.hp2 HG00597.hp1 HG01516.hp1 others(22): Show |
intron_variant | MODIFIER | c.70-20307G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159166335 | ||||||
| chr4:159166559
|
A | T | 3 | a0001c0001t0006g0183a0001c0001t0006g0184a0001c0002t0003g0185 | 3 | HG00099.hp1 HG01106.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.70-20083A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159166559 | ||||||
| chr4:159166574
|
T | A | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.70-20068T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159166574 | ||||||
| chr4:159166877
|
G | C | 3 | a0001c0001t0011g0021a0001c0001t0011g0022a0001c0001t0011g0023 | 3 | HG02280.hp2 HG02970.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.70-19765G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159166877 | ||||||
| chr4:159166985
|
C | T | 121 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.70-19657C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159166985 | ||||||
| chr4:159167188
|
G | A | 8 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(5): Show | 8 | HG02559.hp2 HG02647.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.70-19454G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159167188 | ||||||
| chr4:159167227
|
C | T | 8 | a0001c0001t0002g0001a0001c0001t0002g0025a0001c0001t0002g0060others(5): Show | 8 | HG00438.hp2 HG02074.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-19415C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159167227 | ||||||
| chr4:159167230
|
G | C | 1 | a0001c0001t0008g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.70-19412G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159167230 | ||||||
| chr4:159167250
|
T | G | 1 | a0001c0002t0001g0039 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.70-19392T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159167250 | ||||||
| chr4:159167350
|
G | A | 11 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(8): Show | 11 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.70-19292G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159167350 | ||||||
| chr4:159167449
|
C | T | 1 | a0001c0004t0001g0020 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.70-19193C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159167449 | ||||||
| chr4:159167450
|
G | A | 1 | a0001c0001t0006g0187 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.70-19192G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159167450 | ||||||
| chr4:159167872
|
T | C | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-18770T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159167872 | ||||||
| chr4:159168020
|
G | A | 1 | a0001c0003t0017g0117 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.70-18622G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159168020 | ||||||
| chr4:159168028
|
T | C | 2 | a0001c0001t0002g0005a0001c0001t0025g0081 | 2 | HG03209.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.70-18614T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159168028 | ||||||
| chr4:159168312
|
A | T | 76 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(73): Show | 76 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.70-18330A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159168312 | ||||||
| chr4:159168490
|
C | G | 1 | a0001c0003t0017g0117 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.70-18152C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159168490 | ||||||
| chr4:159168541
|
T | C | 3 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085 | 3 | HG02559.hp2 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.70-18101T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159168541 | ||||||
| chr4:159168616
|
A | G | 2 | a0001c0001t0015g0190a0001c0001t0015g0191 | 2 | HG01099.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.70-18026A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159168616 | ||||||
| chr4:159168758
|
A | G | 1 | a0001c0002t0001g0157 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.70-17884A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159168758 | ||||||
| chr4:159168973
|
A | G | 44 | a0001c0001t0002g0091a0001c0001t0002g0145a0001c0001t0006g0161others(41): Show | 44 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.70-17669A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159168973 | ||||||
| chr4:159169020
|
A | T | 44 | a0001c0001t0002g0091a0001c0001t0002g0145a0001c0001t0006g0161others(41): Show | 44 | HG00099.hp1 HG00280.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.70-17622A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159169020 | ||||||
| chr4:159169075
|
A | G | 7 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0005g0086others(4): Show | 7 | HG02559.hp2 HG02647.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-17567A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159169075 | ||||||
| chr4:159169104
|
C | G | 3 | a0001c0001t0002g0071a0001c0001t0009g0058a0001c0001t0009g0059 | 3 | HG02258.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.70-17538C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159169104 | ||||||
| chr4:159169178
|
A | AC | 89 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(86): Show | 89 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.70-17458dupC | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159169178 | |||||
| chr4:159169199
|
A | G | 1 | a0001c0002t0001g0014 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.70-17443A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159169199 | ||||||
| chr4:159169222
|
A | G | 1 | a0001c0002t0001g0069 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.70-17420A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159169222 | ||||||
| chr4:159169242
|
GA | G | 94 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(91): Show | 94 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.70-17392delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159169242 | |||||
| chr4:159169285
|
A | G | 8 | a0001c0001t0002g0001a0001c0001t0002g0025a0001c0001t0002g0060others(5): Show | 8 | HG00438.hp2 HG02074.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-17357A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159169285 | ||||||
| chr4:159169769
|
G | A | 1 | a0001c0002t0001g0102 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.70-16873G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159169769 | ||||||
| chr4:159169919
|
T | G | 1 | a0001c0002t0001g0069 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.70-16723T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159169919 | ||||||
| chr4:159170071
|
A | G | 26 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(23): Show | 26 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.70-16571A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159170071 | ||||||
| chr4:159170081
|
C | CT | 104 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(101): Show | 104 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.70-16548dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159170081 | |||||
| chr4:159170083
|
T | C | 1 | a0001c0001t0002g0118 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.70-16559T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159170083 | ||||||
| chr4:159170241
|
G | T | 107 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(104): Show | 107 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.70-16401G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159170241 | ||||||
| chr4:159170503
|
C | T | 107 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(104): Show | 107 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.70-16139C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159170503 | ||||||
| chr4:159170504
|
G | C | 1 | a0001c0002t0001g0013 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.70-16138G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159170504 | ||||||
| chr4:159170668
|
G | A | 1 | a0001c0001t0028g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.70-15974G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159170668 | ||||||
| chr4:159170852
|
CTTTAT | C | 49 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(46): Show | 49 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.70-15786_70-15782d others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159170852 | |||||
| chr4:159171055
|
A | G | 4 | a0001c0001t0002g0071a0001c0001t0011g0021a0001c0001t0011g0022others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-15587A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159171055 | ||||||
| chr4:159171153
|
G | A | 107 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(104): Show | 107 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.70-15489G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159171153 | ||||||
| chr4:159171251
|
G | A | 1 | a0001c0003t0004g0064 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.70-15391G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159171251 | ||||||
| chr4:159171370
|
T | C | 33 | a0001c0001t0002g0001a0001c0001t0002g0025a0001c0001t0002g0060others(30): Show | 33 | HG00438.hp2 HG00597.hp1 HG01516.hp1 others(30): Show |
intron_variant | MODIFIER | c.70-15272T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159171370 | ||||||
| chr4:159171392
|
C | T | 18 | a0001c0001t0002g0001a0001c0001t0002g0025a0001c0001t0002g0060others(15): Show | 18 | HG00438.hp2 HG01981.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.70-15250C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159171392 | ||||||
| chr4:159171569
|
G | A | 107 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(104): Show | 107 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.70-15073G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159171569 | ||||||
| chr4:159171684
|
A | AT | 109 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(106): Show | 109 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.70-14947dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159171684 | |||||
| chr4:159171865
|
T | G | 1 | a0001c0001t0008g0112 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.70-14777T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159171865 | ||||||
| chr4:159172190
|
T | G | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70-14452T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159172190 | ||||||
| chr4:159172191
|
T | C | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70-14451T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159172191 | ||||||
| chr4:159172195
|
T | C | 4 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0164others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-14447T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159172195 | ||||||
| chr4:159172293
|
C | G | 1 | a0001c0002t0001g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.70-14349C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159172293 | ||||||
| chr4:159172379
|
A | G | 3 | a0001c0001t0009g0035a0001c0001t0029g0002a0001c0002t0003g0008 | 3 | HG02055.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.70-14263A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159172379 | ||||||
| chr4:159172385
|
C | T | 1 | a0001c0001t0023g0073 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.70-14257C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159172385 | ||||||
| chr4:159172444
|
A | G | 111 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(108): Show | 111 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.70-14198A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159172444 | ||||||
| chr4:159172832
|
T | C | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.70-13810T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159172832 | ||||||
| chr4:159172911
|
TA | T | 108 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(105): Show | 108 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.70-13730delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159172911 | ||||||
| chr4:159173064
|
G | A | 108 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(105): Show | 108 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.70-13578G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159173064 | ||||||
| chr4:159173178
|
A | G | 1 | a0001c0001t0002g0125 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.70-13464A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159173178 | ||||||
| chr4:159173329
|
A | G | 3 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085 | 3 | HG02559.hp2 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.70-13313A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159173329 | ||||||
| chr4:159173373
|
A | G | 1 | a0001c0001t0004g0193 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.70-13269A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159173373 | ||||||
| chr4:159173463
|
A | G | 27 | a0001c0001t0002g0001a0001c0001t0002g0025a0001c0001t0002g0060others(24): Show | 27 | HG00438.hp2 HG00597.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.70-13179A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159173463 | ||||||
| chr4:159173551
|
A | G | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70-13091A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159173551 | ||||||
| chr4:159174154
|
A | C | 111 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(108): Show | 111 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.70-12488A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159174154 | ||||||
| chr4:159174346
|
G | C | 5 | a0001c0001t0006g0161a0001c0001t0006g0175a0001c0001t0006g0177others(2): Show | 5 | HG01099.hp2 HG01891.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-12296G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159174346 | ||||||
| chr4:159174346
|
GATT | G | 6 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0002t0001g0027others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-12293_70-12291d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159174346 | |||||
| chr4:159174648
|
T | C | 4 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0164others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-11994T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159174648 | ||||||
| chr4:159174700
|
A | G | 2 | a0001c0001t0002g0074a0001c0001t0005g0086 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.70-11942A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159174700 | ||||||
| chr4:159174748
|
TTTTC | T | 3 | a0001c0001t0026g0003a0001c0006t0014g0026a0001c0006t0014g0036 | 3 | HG03130.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.70-11882_70-11879d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159174748 | |||||
| chr4:159174757
|
TTTC | T | 45 | a0001c0001t0002g0001a0001c0001t0002g0025a0001c0001t0002g0060others(42): Show | 45 | HG00438.hp2 HG00597.hp1 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.70-11882_70-11880d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159174757 | |||||
| chr4:159174758
|
TTC | T | 60 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(57): Show | 60 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.70-11882_70-11881d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159174758 | |||||
| chr4:159174812
|
A | C | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-11830A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159174812 | ||||||
| chr4:159174901
|
TGCTCGTC others(10): Show |
T | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70-11737_70-11721d others(19): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159174901 | |||||
| chr4:159175296
|
AT | A | 40 | a0001c0001t0002g0029a0001c0001t0002g0066a0001c0001t0002g0079others(37): Show | 40 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.70-11336delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159175296 | |||||
| chr4:159175386
|
C | G | 110 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(107): Show | 110 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.70-11256C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159175386 | ||||||
| chr4:159175696
|
C | T | 1 | a0001c0002t0001g0040 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.70-10946C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159175696 | ||||||
| chr4:159176816
|
G | A | 3 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028 | 3 | HG02970.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.70-9826G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159176816 | ||||||
| chr4:159177165
|
A | C | 108 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(105): Show | 108 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.70-9477A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159177165 | ||||||
| chr4:159177214
|
CT | C | 111 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(108): Show | 111 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.70-9412delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159177214 | |||||
| chr4:159177253
|
G | T | 7 | a0001c0003t0004g0009a0001c0003t0004g0047a0001c0003t0004g0061others(4): Show | 7 | HG02109.hp2 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.70-9389G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159177253 | ||||||
| chr4:159177466
|
C | T | 36 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(33): Show | 36 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.70-9176C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159177466 | ||||||
| chr4:159177541
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.70-9101C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159177541 | ||||||
| chr4:159177546
|
C | T | 107 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(104): Show | 107 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.70-9096C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159177546 | ||||||
| chr4:159177571
|
C | T | 3 | a0001c0002t0003g0188a0001c0002t0003g0189a0001c0002t0003g0192 | 3 | HG01361.hp1 HG01978.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.70-9071C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159177571 | ||||||
| chr4:159177660
|
G | A | 107 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(104): Show | 107 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.70-8982G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159177660 | ||||||
| chr4:159177687
|
A | T | 107 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(104): Show | 107 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.70-8955A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159177687 | ||||||
| chr4:159178218
|
C | T | 3 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028 | 3 | HG02970.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.70-8424C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159178218 | ||||||
| chr4:159178259
|
A | G | 107 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(104): Show | 107 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.70-8383A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159178259 | ||||||
| chr4:159178412
|
C | G | 1 | a0001c0002t0001g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.70-8230C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159178412 | ||||||
| chr4:159178551
|
C | CT | 42 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0025others(39): Show | 42 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.70-8067dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159178551 | |||||
| chr4:159178551
|
C | CTT | 52 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0057others(49): Show | 52 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.70-8068_70-8067dup others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159178551 | |||||
| chr4:159178551
|
C | CTTT | 13 | a0001c0001t0002g0044a0001c0001t0004g0193a0001c0001t0005g0012others(10): Show | 13 | HG00733.hp1 HG01069.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.70-8069_70-8067dup others(3): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159178551 | |||||
| chr4:159178551
|
C | CTTTT | 5 | a0001c0001t0002g0074a0001c0001t0004g0194a0001c0001t0005g0086others(2): Show | 5 | HG03098.hp1 HG03195.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-8070_70-8067dup others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159178551 | |||||
| chr4:159178551
|
CT | C | 6 | a0001c0001t0006g0163a0001c0001t0006g0183a0001c0001t0028g0167others(3): Show | 6 | HG01167.hp1 HG02129.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.70-8067delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159178551 | |||||
| chr4:159178551
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0121 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.70-8077_70-8067del others(11): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159178551 | |||||
| chr4:159178618
|
C | T | 105 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(102): Show | 105 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.70-8024C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159178618 | ||||||
| chr4:159178810
|
C | T | 1 | a0001c0001t0024g0087 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.70-7832C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159178810 | ||||||
| chr4:159178898
|
G | T | 8 | a0001c0001t0005g0024a0001c0001t0026g0003a0001c0002t0001g0075others(5): Show | 8 | HG00597.hp1 HG01516.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-7744G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159178898 | ||||||
| chr4:159178923
|
C | A | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70-7719C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159178923 | ||||||
| chr4:159179013
|
A | G | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70-7629A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159179013 | ||||||
| chr4:159179117
|
T | C | 4 | a0001c0001t0002g0071a0001c0001t0011g0021a0001c0001t0011g0022others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-7525T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159179117 | ||||||
| chr4:159179205
|
C | CA | 147 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.70-7437_70-7436ins others(1): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159179205 | ||||||
| chr4:159179333
|
GAC | G | 45 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(42): Show | 45 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.70-7306_70-7305del others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159179333 | |||||
| chr4:159179402
|
A | AT | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.70-7239dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159179402 | |||||
| chr4:159179475
|
A | G | 1 | a0001c0002t0001g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.70-7167A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159179475 | ||||||
| chr4:159179733
|
A | G | 1 | a0001c0002t0001g0042 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70-6909A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159179733 | ||||||
| chr4:159179903
|
C | T | 1 | a0001c0003t0004g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.70-6739C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159179903 | ||||||
| chr4:159179982
|
G | C | 3 | a0001c0001t0002g0089a0001c0001t0002g0125a0001c0002t0001g0004 | 3 | HG00558.hp1 NA18944.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.70-6660G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159179982 | ||||||
| chr4:159180147
|
G | A | 103 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(100): Show | 103 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.70-6495G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159180147 | ||||||
| chr4:159180152
|
C | G | 191 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.70-6490C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159180152 | ||||||
| chr4:159180513
|
T | C | 2 | a0001c0001t0002g0074a0001c0001t0005g0086 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.70-6129T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159180513 | ||||||
| chr4:159180597
|
A | C | 8 | a0001c0003t0004g0009a0001c0003t0004g0047a0001c0003t0004g0061others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.70-6045A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159180597 | ||||||
| chr4:159180861
|
G | C | 103 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(100): Show | 103 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.70-5781G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159180861 | ||||||
| chr4:159181070
|
G | A | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.70-5572G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159181070 | ||||||
| chr4:159181202
|
C | A | 147 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.70-5440C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159181202 | ||||||
| chr4:159181291
|
G | T | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.70-5351G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159181291 | ||||||
| chr4:159181456
|
A | C | 4 | a0001c0001t0002g0091a0001c0001t0002g0145a0001c0002t0001g0102others(1): Show | 4 | HG00733.hp2 HG01071.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-5186A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159181456 | ||||||
| chr4:159181575
|
CT | C | 50 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0025others(47): Show | 50 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.70-5046delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159181575 | |||||
| chr4:159181575
|
CTT | C | 15 | a0001c0001t0002g0074a0001c0001t0004g0193a0001c0001t0005g0086others(12): Show | 15 | HG01106.hp2 HG01123.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.70-5047_70-5046del others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159181575 | |||||
| chr4:159181575
|
CTTT | C | 45 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(42): Show | 45 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.70-5048_70-5046del others(3): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159181575 | |||||
| chr4:159181599
|
G | T | 1 | a0001c0002t0022g0106 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.70-5043G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159181599 | ||||||
| chr4:159181693
|
G | A | 2 | a0001c0001t0002g0074a0001c0001t0005g0086 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.70-4949G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159181693 | ||||||
| chr4:159181736
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.70-4906C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159181736 | ||||||
| chr4:159181749
|
G | A | 107 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(104): Show | 107 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.70-4893G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159181749 | ||||||
| chr4:159182000
|
T | G | 1 | a0001c0002t0003g0166 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.70-4642T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159182000 | ||||||
| chr4:159182385
|
TC | T | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.70-4256delC | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159182385 | ||||||
| chr4:159182386
|
C | A | 2 | a0001c0001t0002g0074a0001c0001t0005g0086 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.70-4256C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159182386 | ||||||
| chr4:159182386
|
C | CT | 10 | a0001c0001t0002g0005a0001c0001t0002g0088a0001c0001t0002g0090others(7): Show | 10 | HG00280.hp1 HG00438.hp1 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.70-4229dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159182386 | |||||
| chr4:159182386
|
CTTT | C | 96 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0025others(93): Show | 96 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.70-4231_70-4229del others(3): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159182386 | |||||
| chr4:159182386
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70-4238_70-4229del others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159182386 | |||||
| chr4:159182386
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0002g0089 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.70-4242_70-4229del others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159182386 | |||||
| chr4:159182386
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0005g0092a0001c0001t0005g0093 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.70-4243_70-4229del others(15): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | 159182386 | |||||
| chr4:159182387
|
T | A | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.70-4255T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159182387 | ||||||
| chr4:159182398
|
T | A | 4 | a0001c0001t0002g0074a0001c0001t0004g0193a0001c0001t0005g0086others(1): Show | 4 | HG03098.hp1 HG03195.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-4244T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159182398 | ||||||
| chr4:159182402
|
T | A | 4 | a0001c0001t0002g0074a0001c0001t0004g0193a0001c0001t0005g0086others(1): Show | 4 | HG03098.hp1 HG03195.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-4240T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159182402 | ||||||
| chr4:159182413
|
T | G | 1 | a0001c0001t0002g0079 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.70-4229T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159182413 | ||||||
| chr4:159182464
|
C | T | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.70-4178C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159182464 | ||||||
| chr4:159182742
|
G | A | 2 | a0001c0001t0002g0060a0001c0010t0002g0065 | 2 | HG00438.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.70-3900G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159182742 | ||||||
| chr4:159182794
|
G | C | 193 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.70-3848G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159182794 | ||||||
| chr4:159182996
|
G | A | 55 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(52): Show | 55 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.70-3646G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159182996 | ||||||
| chr4:159183203
|
C | T | 1 | a0001c0001t0002g0154 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.70-3439C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159183203 | ||||||
| chr4:159183339
|
A | G | 33 | a0001c0001t0002g0001a0001c0001t0002g0025a0001c0001t0002g0060others(30): Show | 33 | HG00438.hp2 HG00597.hp1 HG01516.hp1 others(30): Show |
intron_variant | MODIFIER | c.70-3303A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159183339 | ||||||
| chr4:159183384
|
G | A | 3 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028 | 3 | HG02970.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.70-3258G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159183384 | ||||||
| chr4:159183387
|
C | T | 104 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(101): Show | 104 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.70-3255C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159183387 | ||||||
| chr4:159183472
|
A | G | 1 | a0001c0001t0002g0025 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.70-3170A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159183472 | ||||||
| chr4:159183484
|
C | T | 2 | a0001c0001t0015g0190a0001c0001t0015g0191 | 2 | HG01099.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.70-3158C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159183484 | ||||||
| chr4:159183692
|
G | A | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.70-2950G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159183692 | ||||||
| chr4:159183754
|
T | A | 5 | a0001c0001t0006g0161a0001c0001t0006g0175a0001c0001t0006g0177others(2): Show | 5 | HG01099.hp2 HG01891.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.70-2888T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159183754 | ||||||
| chr4:159183983
|
C | T | 4 | a0001c0001t0002g0074a0001c0001t0004g0193a0001c0001t0005g0086others(1): Show | 4 | HG03098.hp1 HG03195.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.70-2659C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159183983 | ||||||
| chr4:159184076
|
C | A | 2 | a0001c0001t0005g0012a0001c0001t0005g0051 | 2 | HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.70-2566C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159184076 | ||||||
| chr4:159184176
|
A | G | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70-2466A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159184176 | ||||||
| chr4:159184191
|
G | A | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.70-2451G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159184191 | ||||||
| chr4:159184219
|
T | C | 46 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(43): Show | 46 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.70-2423T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159184219 | ||||||
| chr4:159184295
|
T | C | 46 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(43): Show | 46 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.70-2347T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159184295 | ||||||
| chr4:159184332
|
C | G | 108 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(105): Show | 108 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.70-2310C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159184332 | ||||||
| chr4:159184519
|
T | C | 2 | a0001c0003t0004g0047a0001c0003t0004g0061 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.70-2123T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159184519 | ||||||
| chr4:159184595
|
T | G | 8 | a0001c0003t0004g0009a0001c0003t0004g0047a0001c0003t0004g0061others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.70-2047T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159184595 | ||||||
| chr4:159184652
|
G | A | 2 | a0001c0002t0030g0137a0001c0006t0014g0036 | 2 | HG01099.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.70-1990G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159184652 | ||||||
| chr4:159185009
|
T | A | 4 | a0001c0001t0007g0094a0001c0001t0007g0095a0001c0001t0007g0127others(1): Show | 4 | HG01123.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.70-1633T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159185009 | ||||||
| chr4:159185198
|
A | T | 103 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(100): Show | 103 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.70-1444A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159185198 | ||||||
| chr4:159185240
|
A | G | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.70-1402A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159185240 | ||||||
| chr4:159185542
|
T | C | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70-1100T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159185542 | ||||||
| chr4:159185544
|
A | G | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70-1098A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159185544 | ||||||
| chr4:159185953
|
A | C | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.70-689A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159185953 | ||||||
| chr4:159186224
|
A | T | 1 | a0001c0001t0002g0001 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.70-418A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159186224 | ||||||
| chr4:159186405
|
A | C | 19 | a0001c0001t0002g0071a0001c0001t0009g0035a0001c0001t0010g0155others(16): Show | 19 | HG00735.hp1 HG01081.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.70-237A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159186405 | ||||||
| chr4:159186511
|
T | G | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.70-131T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | chr4 | 159186511 | ||||||
| chr4:159186766
|
T | C | 104 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(101): Show | 104 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.140+54T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159186766 | ||||||
| chr4:159186836
|
A | G | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.140+124A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159186836 | ||||||
| chr4:159186979
|
A | C | 2 | a0001c0001t0002g0074a0001c0001t0005g0086 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.140+267A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159186979 | ||||||
| chr4:159187128
|
T | G | 45 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(42): Show | 45 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.140+416T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159187128 | ||||||
| chr4:159187368
|
C | T | 2 | a0001c0001t0002g0074a0001c0001t0005g0086 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.140+656C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159187368 | ||||||
| chr4:159187617
|
G | C | 2 | a0001c0002t0001g0017a0001c0002t0001g0052 | 2 | HG01943.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.140+905G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159187617 | ||||||
| chr4:159187618
|
C | A | 2 | a0001c0002t0001g0017a0001c0002t0001g0052 | 2 | HG01943.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.140+906C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159187618 | ||||||
| chr4:159187619
|
C | T | 2 | a0001c0002t0001g0017a0001c0002t0001g0052 | 2 | HG01943.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.140+907C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159187619 | ||||||
| chr4:159188050
|
A | G | 1 | a0001c0001t0020g0120 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.140+1338A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159188050 | ||||||
| chr4:159188084
|
A | AGCAAGAA others(308): Show |
3 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028 | 3 | HG02970.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.140+1387_140+1388i others(317): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr4 | 159188084 | |||||
| chr4:159188181
|
C | T | 1 | a0001c0001t0006g0161 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.140+1469C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159188181 | ||||||
| chr4:159188252
|
A | G | 1 | a0001c0001t0005g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.140+1540A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159188252 | ||||||
| chr4:159188253
|
A | G | 1 | a0001c0001t0006g0175 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.140+1541A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159188253 | ||||||
| chr4:159188271
|
T | G | 2 | a0001c0001t0002g0074a0001c0001t0005g0086 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.140+1559T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159188271 | ||||||
| chr4:159188287
|
T | C | 46 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(43): Show | 46 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.140+1575T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159188287 | ||||||
| chr4:159188334
|
G | T | 1 | a0001c0001t0002g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.140+1622G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159188334 | ||||||
| chr4:159188510
|
A | C | 1 | a0001c0001t0002g0142 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.140+1798A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159188510 | ||||||
| chr4:159188663
|
C | CA | 40 | a0001c0001t0002g0074a0001c0001t0004g0193a0001c0001t0005g0086others(37): Show | 40 | HG00099.hp1 HG00280.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.140+1966dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr4 | 159188663 | |||||
| chr4:159188854
|
A | C | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.140+2142A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159188854 | ||||||
| chr4:159188885
|
G | A | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.140+2173G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159188885 | ||||||
| chr4:159188991
|
A | G | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.140+2279A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159188991 | ||||||
| chr4:159189033
|
T | TTAGA | 108 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(105): Show | 108 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.140+2323_140+2324i others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr4 | 159189033 | |||||
| chr4:159189085
|
T | C | 3 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0003g0186 | 3 | HG01516.hp2 HG01517.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.140+2373T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159189085 | ||||||
| chr4:159189150
|
T | C | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.140+2438T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159189150 | ||||||
| chr4:159189150
|
T | G | 1 | a0001c0002t0001g0006 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.140+2438T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159189150 | ||||||
| chr4:159189265
|
C | T | 3 | a0001c0001t0008g0033a0001c0001t0008g0041a0001c0002t0001g0050 | 3 | HG02145.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.140+2553C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159189265 | ||||||
| chr4:159189337
|
A | G | 1 | a0001c0002t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.140+2625A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159189337 | ||||||
| chr4:159189346
|
T | G | 32 | a0001c0001t0002g0001a0001c0001t0002g0025a0001c0001t0002g0060others(29): Show | 32 | HG00438.hp2 HG00597.hp1 HG01516.hp1 others(29): Show |
intron_variant | MODIFIER | c.140+2634T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159189346 | ||||||
| chr4:159189476
|
AT | A | 26 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(23): Show | 26 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.140+2765delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159189476 | ||||||
| chr4:159189771
|
T | TTA | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+3060_140+3061i others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr4 | 159189771 | |||||
| chr4:159189775
|
T | TGTC | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+3063_140+3064i others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159189775 | ||||||
| chr4:159189839
|
A | G | 1 | a0001c0001t0002g0090 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.140+3127A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159189839 | ||||||
| chr4:159189895
|
T | C | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.140+3183T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159189895 | ||||||
| chr4:159189969
|
A | G | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141-3231A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159189969 | ||||||
| chr4:159190015
|
A | G | 111 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(108): Show | 111 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.141-3185A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159190015 | ||||||
| chr4:159190050
|
A | G | 2 | a0001c0001t0005g0092a0001c0001t0005g0093 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.141-3150A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159190050 | ||||||
| chr4:159190084
|
G | A | 104 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(101): Show | 104 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.141-3116G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159190084 | ||||||
| chr4:159190400
|
G | T | 1 | a0001c0001t0009g0059 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.141-2800G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159190400 | ||||||
| chr4:159190752
|
A | T | 109 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0025others(106): Show | 109 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.141-2448A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159190752 | ||||||
| chr4:159190833
|
CAT | C | 3 | a0001c0001t0033g0113a0001c0001t0034g0115a0001c0011t0032g0114 | 3 | HG02257.hp1 HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.141-2366_141-2365d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159190833 | ||||||
| chr4:159190861
|
A | C | 4 | a0001c0001t0002g0091a0001c0001t0002g0145a0001c0002t0001g0102others(1): Show | 4 | HG00733.hp2 HG01071.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-2339A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159190861 | ||||||
| chr4:159191144
|
A | C | 19 | a0001c0001t0002g0071a0001c0001t0009g0035a0001c0001t0010g0155others(16): Show | 19 | HG00735.hp1 HG01081.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.141-2056A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159191144 | ||||||
| chr4:159191168
|
TA | T | 4 | a0001c0001t0002g0074a0001c0001t0004g0193a0001c0001t0005g0086others(1): Show | 4 | HG03098.hp1 HG03195.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-2031delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159191168 | ||||||
| chr4:159191171
|
A | G | 4 | a0001c0001t0002g0074a0001c0001t0004g0193a0001c0001t0005g0086others(1): Show | 4 | HG03098.hp1 HG03195.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-2029A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159191171 | ||||||
| chr4:159191178
|
A | G | 6 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0002t0001g0027others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-2022A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159191178 | ||||||
| chr4:159191203
|
GA | G | 55 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(52): Show | 55 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.141-1987delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr4 | 159191203 | |||||
| chr4:159191280
|
G | A | 109 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0025others(106): Show | 109 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.141-1920G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159191280 | ||||||
| chr4:159191470
|
A | G | 2 | a0001c0001t0002g0074a0001c0001t0005g0086 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.141-1730A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159191470 | ||||||
| chr4:159191564
|
C | T | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141-1636C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159191564 | ||||||
| chr4:159191600
|
G | A | 1 | a0001c0002t0003g0188 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.141-1600G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159191600 | ||||||
| chr4:159191636
|
G | A | 4 | a0001c0001t0002g0074a0001c0001t0004g0193a0001c0001t0005g0086others(1): Show | 4 | HG03098.hp1 HG03195.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-1564G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159191636 | ||||||
| chr4:159191744
|
A | G | 2 | a0001c0002t0001g0030a0001c0002t0001g0031 | 2 | HG00639.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.141-1456A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159191744 | ||||||
| chr4:159191846
|
A | G | 1 | a0001c0002t0001g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.141-1354A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159191846 | ||||||
| chr4:159192069
|
C | T | 3 | a0001c0001t0031g0116a0001c0007t0016g0140a0001c0007t0016g0141 | 3 | HG01884.hp1 HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.141-1131C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159192069 | ||||||
| chr4:159192240
|
A | G | 1 | a0001c0001t0009g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.141-960A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159192240 | ||||||
| chr4:159192281
|
C | T | 1 | a0001c0003t0004g0064 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.141-919C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159192281 | ||||||
| chr4:159192302
|
CA | C | 2 | a0001c0001t0002g0025a0001c0001t0005g0049 | 2 | NA18955.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.141-896delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr4 | 159192302 | |||||
| chr4:159192763
|
T | C | 2 | a0001c0001t0002g0074a0001c0001t0005g0086 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.141-437T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159192763 | ||||||
| chr4:159192800
|
C | T | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.141-400C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159192800 | ||||||
| chr4:159192975
|
C | T | 1 | a0001c0002t0001g0152 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.141-225C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159192975 | ||||||
| chr4:159193125
|
G | C | 148 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(145): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.141-75G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159193125 | ||||||
| chr4:159193136
|
G | A | 4 | a0001c0001t0002g0074a0001c0001t0004g0193a0001c0001t0005g0086others(1): Show | 4 | HG03098.hp1 HG03195.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.141-64G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 2/29 | chr4 | 159193136 | ||||||
| chr4:159193283
|
A | G | 3 | a0001c0001t0002g0074a0001c0001t0005g0086a0001c0002t0001g0152 | 3 | HG03098.hp1 HG03195.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.197+27A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159193283 | ||||||
| chr4:159193610
|
A | G | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.197+354A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159193610 | ||||||
| chr4:159193683
|
T | G | 3 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028 | 3 | HG02970.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.197+427T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159193683 | ||||||
| chr4:159193785
|
A | T | 1 | a0001c0007t0016g0140 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.197+529A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159193785 | ||||||
| chr4:159194065
|
G | A | 102 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0025others(99): Show | 102 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.197+809G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159194065 | ||||||
| chr4:159194339
|
C | G | 1 | a0001c0002t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.197+1083C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159194339 | ||||||
| chr4:159194683
|
C | CT | 43 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0071others(40): Show | 43 | HG00438.hp2 HG00597.hp1 HG01516.hp1 others(40): Show |
intron_variant | MODIFIER | c.197+1436dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159194683 | |||||
| chr4:159194766
|
A | G | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.197+1510A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159194766 | ||||||
| chr4:159195002
|
G | A | 4 | a0001c0001t0002g0074a0001c0001t0004g0193a0001c0001t0005g0086others(1): Show | 4 | HG03098.hp1 HG03195.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+1746G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159195002 | ||||||
| chr4:159195133
|
A | G | 1 | a0001c0002t0003g0160 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.197+1877A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159195133 | ||||||
| chr4:159195309
|
C | T | 110 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0025others(107): Show | 110 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.197+2053C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159195309 | ||||||
| chr4:159195443
|
C | T | 4 | a0001c0002t0001g0075a0001c0002t0001g0153a0001c0002t0001g0158others(1): Show | 4 | HG00597.hp1 HG01516.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+2187C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159195443 | ||||||
| chr4:159195506
|
G | A | 3 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0003g0186 | 3 | HG01516.hp2 HG01517.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.197+2250G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159195506 | ||||||
| chr4:159195733
|
C | T | 4 | a0001c0002t0001g0075a0001c0002t0001g0153a0001c0002t0001g0158others(1): Show | 4 | HG00597.hp1 HG01516.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+2477C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159195733 | ||||||
| chr4:159195781
|
C | T | 2 | a0001c0001t0002g0089a0001c0001t0002g0125 | 2 | HG00558.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.197+2525C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159195781 | ||||||
| chr4:159195782
|
G | A | 1 | a0001c0002t0003g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.197+2526G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159195782 | ||||||
| chr4:159195872
|
C | A | 1 | a0001c0001t0002g0098 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.197+2616C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159195872 | ||||||
| chr4:159195875
|
G | GT | 29 | a0001c0001t0002g0029a0001c0001t0002g0088a0001c0001t0002g0097others(26): Show | 29 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.197+2648dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159195875 | |||||
| chr4:159195875
|
G | GTT | 13 | a0001c0001t0002g0001a0001c0001t0006g0161a0001c0001t0006g0163others(10): Show | 13 | HG01099.hp1 HG01167.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.197+2647_197+2648d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159195875 | |||||
| chr4:159195875
|
G | GTTT | 6 | a0001c0001t0002g0132a0001c0001t0006g0175a0001c0001t0006g0177others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.197+2646_197+2648d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159195875 | |||||
| chr4:159195875
|
GTT | G | 7 | a0001c0001t0002g0060a0001c0001t0002g0071a0001c0001t0009g0058others(4): Show | 7 | HG00438.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.197+2647_197+2648d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159195875 | |||||
| chr4:159195875
|
GTTT | G | 24 | a0001c0001t0002g0025a0001c0001t0005g0024a0001c0001t0005g0049others(21): Show | 24 | HG00597.hp1 HG01516.hp1 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.197+2646_197+2648d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159195875 | |||||
| chr4:159195875
|
GTTTTT | G | 21 | a0001c0001t0002g0057a0001c0001t0005g0012a0001c0001t0005g0051others(18): Show | 21 | HG01123.hp1 HG01891.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.197+2644_197+2648d others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159195875 | |||||
| chr4:159195875
|
GTTTTTT | G | 45 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(42): Show | 45 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.197+2643_197+2648d others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159195875 | |||||
| chr4:159195887
|
T | G | 1 | a0001c0001t0002g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.197+2631T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159195887 | ||||||
| chr4:159195903
|
T | C | 6 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0002t0001g0027others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.197+2647T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159195903 | ||||||
| chr4:159195904
|
T | C | 45 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(42): Show | 45 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.197+2648T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159195904 | ||||||
| chr4:159196030
|
A | C | 1 | a0001c0002t0030g0137 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.197+2774A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159196030 | ||||||
| chr4:159196055
|
A | G | 4 | a0001c0001t0002g0074a0001c0001t0004g0193a0001c0001t0005g0086others(1): Show | 4 | HG03098.hp1 HG03195.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+2799A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159196055 | ||||||
| chr4:159196058
|
G | A | 2 | a0001c0001t0002g0074a0001c0001t0005g0086 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.197+2802G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159196058 | ||||||
| chr4:159196190
|
G | C | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.197+2934G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159196190 | ||||||
| chr4:159196315
|
C | A | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.197+3059C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159196315 | ||||||
| chr4:159196549
|
CT | C | 55 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(52): Show | 55 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.197+3294delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159196549 | ||||||
| chr4:159196852
|
C | T | 45 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(42): Show | 45 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.197+3596C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159196852 | ||||||
| chr4:159196962
|
G | A | 1 | a0001c0002t0022g0106 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.197+3706G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159196962 | ||||||
| chr4:159196973
|
T | G | 1 | a0001c0002t0001g0158 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.197+3717T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159196973 | ||||||
| chr4:159196995
|
A | G | 1 | a0001c0002t0001g0075 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.197+3739A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159196995 | ||||||
| chr4:159197153
|
G | C | 1 | a0001c0001t0002g0154 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.197+3897G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159197153 | ||||||
| chr4:159197306
|
A | G | 103 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0025others(100): Show | 103 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.197+4050A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159197306 | ||||||
| chr4:159197407
|
T | C | 3 | a0001c0001t0009g0035a0001c0001t0029g0002a0001c0002t0003g0008 | 3 | HG02055.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.197+4151T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159197407 | ||||||
| chr4:159197425
|
C | CCA | 111 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0025others(108): Show | 111 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.197+4181_197+4182d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159197425 | |||||
| chr4:159197462
|
C | T | 1 | a0001c0002t0012g0156 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.197+4206C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159197462 | ||||||
| chr4:159197550
|
C | T | 3 | a0001c0002t0001g0027a0001c0002t0001g0038a0001c0002t0001g0039 | 3 | HG01069.hp2 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.197+4294C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159197550 | ||||||
| chr4:159197603
|
G | A | 1 | a0001c0003t0004g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.197+4347G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159197603 | ||||||
| chr4:159197608
|
G | A | 188 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.197+4352G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159197608 | ||||||
| chr4:159197724
|
G | C | 3 | a0001c0001t0009g0035a0001c0001t0029g0002a0001c0002t0003g0008 | 3 | HG02055.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.197+4468G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159197724 | ||||||
| chr4:159197739
|
A | G | 1 | a0001c0002t0001g0153 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.197+4483A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159197739 | ||||||
| chr4:159197771
|
C | T | 1 | a0001c0001t0028g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.197+4515C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159197771 | ||||||
| chr4:159198193
|
C | A | 18 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0005g0049others(15): Show | 18 | HG00438.hp2 HG01981.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.197+4937C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159198193 | ||||||
| chr4:159198226
|
A | C | 12 | a0001c0001t0009g0035a0001c0001t0010g0155a0001c0001t0010g0162others(9): Show | 12 | HG00735.hp1 HG01081.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.197+4970A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159198226 | ||||||
| chr4:159198232
|
TTTTC | T | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.197+4987_197+4990d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198232 | |||||
| chr4:159198243
|
T | C | 47 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(44): Show | 47 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.197+4987T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159198243 | ||||||
| chr4:159198247
|
CCTTTCTT others(19): Show |
C | 1 | a0001c0001t0008g0062 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.197+5006_197+5031d others(28): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198247 | |||||
| chr4:159198247
|
CCTTTCTT others(23): Show |
C | 4 | a0001c0002t0001g0027a0001c0002t0001g0038a0001c0002t0001g0039others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+5006_197+5035d others(32): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198247 | |||||
| chr4:159198249
|
TTTCTTTC others(15): Show |
T | 2 | a0001c0001t0008g0067a0001c0002t0001g0014 | 2 | HG02165.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.197+5006_197+5027d others(24): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198249 | |||||
| chr4:159198251
|
T | C | 39 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(36): Show | 39 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.197+4995T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159198251 | ||||||
| chr4:159198254
|
TTCTTTC | T | 9 | a0001c0001t0007g0078a0001c0001t0007g0095a0001c0001t0008g0041others(6): Show | 9 | HG00733.hp1 HG01123.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.197+5006_197+5011d others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198254 | |||||
| chr4:159198255
|
T | C | 1 | a0001c0001t0004g0193 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.197+4999T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159198255 | ||||||
| chr4:159198257
|
TTTCTCTT others(7): Show |
T | 3 | a0001c0002t0001g0013a0001c0002t0001g0138a0001c0011t0032g0114 | 3 | HG01258.hp2 HG02257.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.197+5006_197+5019d others(16): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198257 | |||||
| chr4:159198258
|
TTC | T | 12 | a0001c0001t0002g0015a0001c0001t0002g0057a0001c0001t0005g0012others(9): Show | 12 | HG00639.hp1 HG01109.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.197+5006_197+5007d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198258 | |||||
| chr4:159198260
|
C | CTT | 18 | a0001c0001t0002g0010a0001c0001t0002g0044a0001c0001t0005g0051others(15): Show | 18 | HG00642.hp2 HG00738.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.197+5005_197+5006i others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198260 | |||||
| chr4:159198261
|
T | C | 1 | a0001c0003t0004g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.197+5005T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159198261 | ||||||
| chr4:159198261
|
TCTTTCTT others(3): Show |
T | 7 | a0001c0001t0004g0193a0001c0001t0033g0113a0001c0001t0034g0115others(4): Show | 7 | HG00099.hp2 HG02896.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.197+5006_197+5015d others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159198261 | ||||||
| chr4:159198271
|
C | T | 90 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0025others(87): Show | 90 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(87): Show |
intron_variant | MODIFIER | c.197+5015C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159198271 | ||||||
| chr4:159198271
|
CTTCT | C | 9 | a0001c0001t0002g0001a0001c0001t0006g0161a0001c0001t0006g0177others(6): Show | 9 | HG01106.hp1 HG01123.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.197+5078_197+5081d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198271 | |||||
| chr4:159198271
|
CTTCTTTC others(1): Show |
C | 14 | a0001c0001t0002g0079a0001c0001t0006g0175a0001c0001t0009g0146others(11): Show | 14 | HG01099.hp1 HG01099.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.197+5074_197+5081d others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198271 | |||||
| chr4:159198271
|
CTTCTTTC others(5): Show |
C | 8 | a0001c0001t0002g0005a0001c0001t0002g0076a0001c0001t0002g0098others(5): Show | 8 | HG01081.hp1 HG01934.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.197+5070_197+5081d others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198271 | |||||
| chr4:159198271
|
CTTCTTTC others(9): Show |
C | 10 | a0001c0001t0002g0066a0001c0001t0002g0091a0001c0001t0002g0123others(7): Show | 10 | HG00558.hp2 HG01258.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.197+5066_197+5081d others(18): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198271 | |||||
| chr4:159198271
|
CTTCTTTC others(13): Show |
C | 12 | a0001c0001t0002g0088a0001c0001t0002g0096a0001c0001t0002g0097others(9): Show | 12 | HG00280.hp1 HG00735.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.197+5062_197+5081d others(22): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198271 | |||||
| chr4:159198271
|
CTTCTTTC others(17): Show |
C | 20 | a0001c0001t0002g0029a0001c0001t0002g0089a0001c0001t0002g0090others(17): Show | 20 | HG00438.hp1 HG00558.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.197+5058_197+5081d others(26): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198271 | |||||
| chr4:159198271
|
CTTCTTTC others(21): Show |
C | 4 | a0001c0001t0006g0187a0001c0002t0001g0006a0001c0002t0001g0107others(1): Show | 4 | HG00597.hp2 HG00738.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+5054_197+5081d others(30): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198271 | |||||
| chr4:159198271
|
CTTCTTTC others(25): Show |
C | 1 | a0001c0001t0002g0099 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.197+5050_197+5081d others(34): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198271 | |||||
| chr4:159198271
|
CTTCTTTC others(33): Show |
C | 3 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028 | 3 | HG02970.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.197+5042_197+5081d others(42): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198271 | |||||
| chr4:159198273
|
T | C | 1 | a0001c0002t0001g0014 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.197+5017T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159198273 | ||||||
| chr4:159198282
|
CTTTCTTT others(23): Show |
C | 3 | a0001c0001t0026g0003a0001c0006t0014g0026a0001c0006t0014g0036 | 3 | HG03130.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.197+5028_197+5057d others(32): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198282 | |||||
| chr4:159198286
|
CTTTCTTT others(19): Show |
C | 21 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0071others(18): Show | 21 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.197+5032_197+5057d others(28): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198286 | |||||
| chr4:159198286
|
CTTTCTTT others(23): Show |
C | 15 | a0001c0001t0009g0035a0001c0001t0009g0058a0001c0001t0009g0059others(12): Show | 15 | HG01516.hp1 HG01981.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.197+5032_197+5061d others(32): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198286 | |||||
| chr4:159198286
|
CTTTCTTT others(31): Show |
C | 1 | a0001c0002t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.197+5032_197+5069d others(40): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198286 | |||||
| chr4:159198288
|
T | C | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.197+5032T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159198288 | ||||||
| chr4:159198290
|
C | T | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.197+5034C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159198290 | ||||||
| chr4:159198290
|
CTTTCTTT others(15): Show |
C | 2 | a0001c0003t0017g0117a0001c0005t0012g0105 | 2 | HG01081.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.197+5036_197+5057d others(24): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198290 | |||||
| chr4:159198290
|
CTTTCTTT others(19): Show |
C | 4 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0164others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+5036_197+5061d others(28): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198290 | |||||
| chr4:159198294
|
CTTTCTTT others(11): Show |
C | 1 | a0001c0003t0019g0135 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.197+5040_197+5057d others(20): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198294 | |||||
| chr4:159198306
|
CTTTCTTT others(22): Show |
C | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.197+5054_197+5082d others(31): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198306 | |||||
| chr4:159198314
|
CTT | C | 50 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(47): Show | 50 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.197+5060_197+5061d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198314 | |||||
| chr4:159198316
|
T | TTC | 3 | a0001c0002t0001g0042a0001c0002t0001g0100a0001c0003t0004g0019 | 3 | HG01496.hp2 HG06807.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.197+5062_197+5063d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198316 | |||||
| chr4:159198316
|
T | TTCTTTCT others(3): Show |
1 | a0001c0001t0002g0074 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.197+5062_197+5071d others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198316 | |||||
| chr4:159198320
|
T | TTC | 4 | a0001c0001t0005g0051a0001c0002t0001g0052a0001c0002t0001g0056others(1): Show | 4 | HG00642.hp2 HG01978.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+5066_197+5067d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198320 | |||||
| chr4:159198334
|
CT | C | 100 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0025others(97): Show | 100 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.197+5083delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198334 | |||||
| chr4:159198335
|
T | TTTC | 6 | a0001c0001t0002g0074a0001c0001t0005g0051a0001c0001t0005g0086others(3): Show | 6 | HG00642.hp2 HG01978.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.197+5081_197+5082i others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198335 | |||||
| chr4:159198376
|
T | TTTCC | 56 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(53): Show | 56 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.197+5138_197+5141d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198376 | |||||
| chr4:159198413
|
C | CCT | 4 | a0001c0001t0002g0132a0001c0001t0005g0092a0001c0001t0005g0093others(1): Show | 4 | HG02970.hp1 HG03239.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+5176_197+5177d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198413 | |||||
| chr4:159198413
|
CCT | C | 53 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0004g0194others(50): Show | 53 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.197+5176_197+5177d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198413 | |||||
| chr4:159198413
|
CCTCT | C | 8 | a0001c0001t0002g0071a0001c0001t0006g0163a0001c0001t0011g0021others(5): Show | 8 | HG02129.hp1 HG02258.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.197+5174_197+5177d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198413 | |||||
| chr4:159198413
|
CCTCTCT | C | 4 | a0001c0001t0002g0074a0001c0001t0004g0193a0001c0001t0005g0086others(1): Show | 4 | HG03098.hp1 HG03195.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+5172_197+5177d others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198413 | |||||
| chr4:159198428
|
CTCTCTT | C | 45 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(42): Show | 45 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.197+5176_197+5181d others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198428 | |||||
| chr4:159198655
|
AG | A | 4 | a0001c0002t0001g0075a0001c0002t0001g0153a0001c0002t0001g0158others(1): Show | 4 | HG00597.hp1 HG01516.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+5401delG | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159198655 | |||||
| chr4:159198899
|
G | A | 3 | a0001c0003t0004g0063a0001c0003t0004g0064a0001c0003t0004g0068 | 3 | HG02055.hp1 HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.197+5643G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159198899 | ||||||
| chr4:159199057
|
C | CA | 32 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0066others(29): Show | 32 | HG00438.hp2 HG01981.hp1 HG02040.hp1 others(29): Show |
intron_variant | MODIFIER | c.197+5822dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159199057 | |||||
| chr4:159199057
|
CA | C | 23 | a0001c0001t0006g0170a0001c0001t0024g0087a0001c0001t0027g0104others(20): Show | 23 | HG00280.hp2 HG01081.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.197+5822delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159199057 | |||||
| chr4:159199057
|
CAA | C | 9 | a0001c0001t0006g0183a0001c0001t0006g0184a0001c0002t0001g0134others(6): Show | 9 | HG00099.hp1 HG00597.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.197+5821_197+5822d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159199057 | |||||
| chr4:159199137
|
G | T | 2 | a0001c0001t0002g0109a0001c0001t0002g0123 | 2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.197+5881G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159199137 | ||||||
| chr4:159199308
|
A | G | 30 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(27): Show | 30 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.197+6052A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159199308 | ||||||
| chr4:159199373
|
A | G | 1 | a0001c0001t0006g0183 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.197+6117A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159199373 | ||||||
| chr4:159199470
|
G | GT | 51 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0071others(48): Show | 51 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.197+6225dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159199470 | |||||
| chr4:159199522
|
A | T | 55 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(52): Show | 55 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.197+6266A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159199522 | ||||||
| chr4:159199586
|
G | T | 26 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0005g0024others(23): Show | 26 | HG00438.hp2 HG00597.hp1 HG01516.hp1 others(23): Show |
intron_variant | MODIFIER | c.197+6330G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159199586 | ||||||
| chr4:159199594
|
G | A | 1 | a0001c0002t0003g0169 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.197+6338G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159199594 | ||||||
| chr4:159199608
|
T | C | 5 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0164others(2): Show | 5 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.197+6352T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159199608 | ||||||
| chr4:159199695
|
G | T | 1 | a0001c0001t0009g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.197+6439G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159199695 | ||||||
| chr4:159199853
|
GAA | G | 3 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0165 | 3 | HG01884.hp2 HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.197+6599_197+6600d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159199853 | |||||
| chr4:159199856
|
A | T | 3 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0165 | 3 | HG01884.hp2 HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.197+6600A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159199856 | ||||||
| chr4:159199858
|
A | T | 3 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0165 | 3 | HG01884.hp2 HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.197+6602A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159199858 | ||||||
| chr4:159199859
|
G | T | 3 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0165 | 3 | HG01884.hp2 HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.197+6603G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159199859 | ||||||
| chr4:159199860
|
G | T | 3 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0165 | 3 | HG01884.hp2 HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.197+6604G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159199860 | ||||||
| chr4:159199862
|
T | TA | 3 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0165 | 3 | HG01884.hp2 HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.197+6606_197+6607i others(3): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159199862 | ||||||
| chr4:159200015
|
C | G | 1 | a0001c0001t0002g0057 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.197+6759C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159200015 | ||||||
| chr4:159200046
|
A | ATC | 3 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028 | 3 | HG02970.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.197+6804_197+6805d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159200046 | |||||
| chr4:159200046
|
A | ATCTC | 27 | a0001c0001t0002g0025a0001c0001t0004g0194a0001c0001t0005g0024others(24): Show | 27 | HG00597.hp1 HG01516.hp1 HG01981.hp1 others(24): Show |
intron_variant | MODIFIER | c.197+6802_197+6805d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159200046 | |||||
| chr4:159200046
|
A | ATCTCTC | 13 | a0001c0001t0009g0035a0001c0001t0010g0155a0001c0001t0010g0162others(10): Show | 13 | HG00735.hp1 HG01081.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.197+6800_197+6805d others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159200046 | |||||
| chr4:159200046
|
A | ATCTCTCT others(1): Show |
5 | a0001c0001t0002g0071a0001c0001t0011g0021a0001c0001t0011g0022others(2): Show | 5 | HG02258.hp2 HG02280.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.197+6798_197+6805d others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159200046 | |||||
| chr4:159200058
|
C | A | 2 | a0001c0002t0001g0027a0001c0002t0001g0038 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.197+6802C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159200058 | ||||||
| chr4:159200060
|
C | A | 4 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0002t0001g0027others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+6804C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159200060 | ||||||
| chr4:159200060
|
C | CTCTCTA | 2 | a0001c0001t0027g0104a0001c0003t0019g0135 | 2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.197+6805_197+6806i others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159200060 | |||||
| chr4:159200062
|
A | C | 85 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(82): Show | 85 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.197+6806A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159200062 | ||||||
| chr4:159200064
|
A | C | 11 | a0001c0001t0002g0071a0001c0001t0005g0024a0001c0001t0010g0162others(8): Show | 11 | HG02258.hp2 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.197+6808A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159200064 | ||||||
| chr4:159200286
|
G | C | 54 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(51): Show | 54 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.197+7030G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159200286 | ||||||
| chr4:159200311
|
A | G | 1 | a0001c0002t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.197+7055A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159200311 | ||||||
| chr4:159200363
|
G | A | 2 | a0001c0001t0002g0015a0001c0002t0001g0034 | 2 | HG00738.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.197+7107G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159200363 | ||||||
| chr4:159200559
|
A | G | 4 | a0001c0001t0002g0074a0001c0001t0004g0193a0001c0001t0005g0086others(1): Show | 4 | HG03098.hp1 HG03195.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+7303A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159200559 | ||||||
| chr4:159200572
|
TA | T | 19 | a0001c0001t0002g0071a0001c0001t0009g0035a0001c0001t0010g0155others(16): Show | 19 | HG00735.hp1 HG01081.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.197+7325delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159200572 | |||||
| chr4:159200697
|
A | G | 5 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0002t0001g0027others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.197+7441A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159200697 | ||||||
| chr4:159200877
|
T | C | 48 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0071others(45): Show | 48 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.197+7621T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159200877 | ||||||
| chr4:159200999
|
T | A | 1 | a0001c0001t0006g0175 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.197+7743T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159200999 | ||||||
| chr4:159201261
|
G | A | 1 | a0001c0001t0006g0187 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.197+8005G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159201261 | ||||||
| chr4:159201280
|
G | T | 1 | a0001c0001t0002g0099 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.197+8024G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159201280 | ||||||
| chr4:159201544
|
G | T | 3 | a0001c0002t0001g0004a0001c0002t0001g0037a0001c0002t0001g0048 | 3 | NA18961.hp2 NA19005.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.197+8288G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159201544 | ||||||
| chr4:159201765
|
G | A | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.197+8509G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159201765 | ||||||
| chr4:159201899
|
G | A | 1 | a0001c0001t0010g0162 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.198-8601G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159201899 | ||||||
| chr4:159201911
|
A | G | 2 | a0001c0001t0002g0145a0001c0008t0002g0119 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.198-8589A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159201911 | ||||||
| chr4:159201930
|
C | T | 2 | a0001c0001t0015g0190a0001c0001t0015g0191 | 2 | HG01099.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.198-8570C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159201930 | ||||||
| chr4:159202106
|
G | A | 1 | a0001c0001t0002g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.198-8394G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159202106 | ||||||
| chr4:159202153
|
C | T | 2 | a0001c0001t0002g0025a0001c0001t0005g0049 | 2 | NA18955.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.198-8347C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159202153 | ||||||
| chr4:159202185
|
G | A | 1 | a0001c0001t0006g0184 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.198-8315G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159202185 | ||||||
| chr4:159202432
|
G | A | 2 | a0001c0001t0002g0096a0001c0001t0002g0142 | 2 | HG00735.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.198-8068G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159202432 | ||||||
| chr4:159202448
|
T | G | 1 | a0001c0001t0002g0044 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.198-8052T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159202448 | ||||||
| chr4:159202534
|
C | T | 47 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0071others(44): Show | 47 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.198-7966C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159202534 | ||||||
| chr4:159202584
|
A | G | 2 | a0001c0001t0002g0060a0001c0010t0002g0065 | 2 | HG00438.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.198-7916A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159202584 | ||||||
| chr4:159202613
|
G | A | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.198-7887G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159202613 | ||||||
| chr4:159202688
|
G | A | 3 | a0001c0001t0031g0116a0001c0007t0016g0140a0001c0007t0016g0141 | 3 | HG01884.hp1 HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.198-7812G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159202688 | ||||||
| chr4:159202742
|
T | C | 107 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0025others(104): Show | 107 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.198-7758T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159202742 | ||||||
| chr4:159202807
|
G | T | 1 | a0001c0001t0025g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.198-7693G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159202807 | ||||||
| chr4:159202833
|
C | T | 2 | a0001c0002t0003g0172a0001c0002t0003g0179 | 2 | HG02897.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.198-7667C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159202833 | ||||||
| chr4:159202882
|
G | A | 47 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0071others(44): Show | 47 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.198-7618G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159202882 | ||||||
| chr4:159202923
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.198-7577T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159202923 | ||||||
| chr4:159203198
|
G | A | 1 | a0001c0001t0029g0002 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.198-7302G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159203198 | ||||||
| chr4:159203255
|
G | T | 56 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(53): Show | 56 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.198-7245G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159203255 | ||||||
| chr4:159203806
|
T | A | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.198-6694T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159203806 | ||||||
| chr4:159204048
|
G | A | 3 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028 | 3 | HG02970.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.198-6452G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159204048 | ||||||
| chr4:159204312
|
A | T | 8 | a0001c0003t0004g0009a0001c0003t0004g0047a0001c0003t0004g0061others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.198-6188A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159204312 | ||||||
| chr4:159204355
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.198-6145C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159204355 | ||||||
| chr4:159204487
|
C | T | 3 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028 | 3 | HG02970.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.198-6013C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159204487 | ||||||
| chr4:159204667
|
G | A | 1 | a0001c0002t0001g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.198-5833G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159204667 | ||||||
| chr4:159204702
|
G | A | 1 | a0001c0002t0003g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.198-5798G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159204702 | ||||||
| chr4:159204737
|
A | T | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.198-5763A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159204737 | ||||||
| chr4:159204975
|
G | A | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.198-5525G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159204975 | ||||||
| chr4:159205127
|
G | C | 59 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(56): Show | 59 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.198-5373G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159205127 | ||||||
| chr4:159205135
|
T | C | 2 | a0001c0001t0002g0089a0001c0001t0002g0125 | 2 | HG00558.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.198-5365T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159205135 | ||||||
| chr4:159205545
|
A | C | 45 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(42): Show | 45 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.198-4955A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159205545 | ||||||
| chr4:159205649
|
C | T | 2 | a0001c0001t0002g0044a0001c0002t0001g0152 | 2 | HG01069.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.198-4851C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159205649 | ||||||
| chr4:159205886
|
T | C | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.198-4614T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159205886 | ||||||
| chr4:159205910
|
A | G | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.198-4590A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159205910 | ||||||
| chr4:159205933
|
C | CT | 5 | a0001c0001t0002g0074a0001c0001t0004g0193a0001c0001t0005g0086others(2): Show | 5 | HG03017.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.198-4554dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159205933 | |||||
| chr4:159206160
|
G | C | 1 | a0001c0002t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.198-4340G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159206160 | ||||||
| chr4:159206177
|
A | G | 110 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0025others(107): Show | 110 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.198-4323A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159206177 | ||||||
| chr4:159206182
|
T | G | 103 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0025others(100): Show | 103 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.198-4318T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159206182 | ||||||
| chr4:159206203
|
G | T | 191 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.198-4297G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159206203 | ||||||
| chr4:159206396
|
G | A | 6 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0002t0001g0027others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-4104G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159206396 | ||||||
| chr4:159206517
|
T | C | 6 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0002t0001g0027others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-3983T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159206517 | ||||||
| chr4:159206548
|
A | G | 55 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(52): Show | 55 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.198-3952A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159206548 | ||||||
| chr4:159206759
|
T | A | 1 | a0001c0001t0008g0067 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.198-3741T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159206759 | ||||||
| chr4:159206764
|
A | C | 2 | a0001c0001t0002g0060a0001c0010t0002g0065 | 2 | HG00438.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.198-3736A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159206764 | ||||||
| chr4:159206884
|
A | G | 1 | a0001c0001t0006g0163 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.198-3616A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159206884 | ||||||
| chr4:159207128
|
A | C | 1 | a0001c0002t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.198-3372A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159207128 | ||||||
| chr4:159207288
|
C | T | 108 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(105): Show | 108 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.198-3212C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159207288 | ||||||
| chr4:159207308
|
G | A | 1 | a0001c0001t0002g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.198-3192G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159207308 | ||||||
| chr4:159207644
|
A | G | 2 | a0001c0001t0002g0074a0001c0001t0005g0086 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.198-2856A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159207644 | ||||||
| chr4:159207705
|
T | C | 105 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(102): Show | 105 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.198-2795T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159207705 | ||||||
| chr4:159208076
|
G | A | 3 | a0001c0001t0033g0113a0001c0001t0034g0115a0001c0011t0032g0114 | 3 | HG02257.hp1 HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.198-2424G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159208076 | ||||||
| chr4:159208139
|
TG | T | 15 | a0001c0001t0009g0035a0001c0001t0010g0155a0001c0001t0010g0162others(12): Show | 15 | HG00735.hp1 HG01081.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.198-2355delG | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159208139 | |||||
| chr4:159208167
|
C | G | 46 | a0001c0001t0002g0060a0001c0001t0002g0071a0001c0001t0004g0194others(43): Show | 46 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.198-2333C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159208167 | ||||||
| chr4:159208722
|
T | G | 2 | a0001c0001t0002g0074a0001c0001t0005g0086 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.198-1778T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159208722 | ||||||
| chr4:159208889
|
A | AT | 32 | a0001c0001t0002g0060a0001c0001t0002g0071a0001c0001t0004g0193others(29): Show | 32 | HG00438.hp2 HG00597.hp1 HG01516.hp1 others(29): Show |
intron_variant | MODIFIER | c.198-1600dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159208889 | |||||
| chr4:159209145
|
G | A | 84 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0025others(81): Show | 84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.198-1355G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159209145 | ||||||
| chr4:159209191
|
C | CA | 6 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0005g0086others(3): Show | 6 | HG01258.hp2 HG02818.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.198-1290dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159209191 | |||||
| chr4:159209191
|
CA | C | 16 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0010g0155others(13): Show | 16 | HG00735.hp1 HG01081.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.198-1290delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159209191 | |||||
| chr4:159209191
|
CAA | C | 45 | a0001c0001t0002g0029a0001c0001t0002g0060a0001c0001t0002g0071others(42): Show | 45 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.198-1291_198-1290d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159209191 | |||||
| chr4:159209191
|
CAAA | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0025others(62): Show | 65 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.198-1292_198-1290d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr4 | 159209191 | |||||
| chr4:159209275
|
A | C | 1 | a0001c0002t0003g0181 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.198-1225A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159209275 | ||||||
| chr4:159209359
|
C | T | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.198-1141C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159209359 | ||||||
| chr4:159209391
|
A | G | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.198-1109A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159209391 | ||||||
| chr4:159209562
|
T | G | 3 | a0001c0001t0009g0035a0001c0001t0029g0002a0001c0002t0003g0008 | 3 | HG02055.hp2 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.198-938T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159209562 | ||||||
| chr4:159210098
|
C | T | 1 | a0001c0002t0001g0034 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.198-402C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 3/29 | chr4 | 159210098 | ||||||
| chr4:159210721
|
A | G | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.281+138A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159210721 | ||||||
| chr4:159210766
|
C | A | 1 | a0001c0002t0003g0008 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.281+183C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159210766 | ||||||
| chr4:159210808
|
G | A | 2 | a0001c0001t0002g0025a0001c0001t0005g0049 | 2 | NA18955.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.281+225G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159210808 | ||||||
| chr4:159210897
|
G | A | 8 | a0001c0003t0004g0009a0001c0003t0004g0047a0001c0003t0004g0061others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.281+314G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159210897 | ||||||
| chr4:159211043
|
T | G | 1 | a0001c0002t0003g0189 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.281+460T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159211043 | ||||||
| chr4:159211276
|
T | G | 3 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028 | 3 | HG02970.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.281+693T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159211276 | ||||||
| chr4:159211428
|
AC | A | 16 | a0001c0001t0009g0035a0001c0001t0010g0155a0001c0001t0010g0162others(13): Show | 16 | HG00735.hp1 HG01081.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.281+846delC | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159211428 | ||||||
| chr4:159211686
|
G | A | 4 | a0001c0001t0002g0074a0001c0001t0004g0193a0001c0001t0005g0086others(1): Show | 4 | HG03098.hp1 HG03195.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.281+1103G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159211686 | ||||||
| chr4:159211767
|
G | A | 3 | a0001c0001t0008g0033a0001c0001t0008g0041a0001c0002t0001g0050 | 3 | HG02145.hp2 HG02486.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.281+1184G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159211767 | ||||||
| chr4:159211807
|
T | C | 1 | a0001c0002t0001g0138 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.281+1224T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159211807 | ||||||
| chr4:159211812
|
G | T | 1 | a0001c0002t0001g0138 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.281+1229G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159211812 | ||||||
| chr4:159211838
|
A | G | 107 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0025others(104): Show | 107 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.281+1255A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159211838 | ||||||
| chr4:159211959
|
A | G | 1 | a0001c0002t0001g0075 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.281+1376A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159211959 | ||||||
| chr4:159212092
|
G | GA | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.281+1511dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159212092 | |||||
| chr4:159212125
|
G | A | 1 | a0001c0005t0005g0016 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.281+1542G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159212125 | ||||||
| chr4:159212249
|
C | G | 4 | a0001c0001t0002g0074a0001c0001t0004g0193a0001c0001t0005g0086others(1): Show | 4 | HG03098.hp1 HG03195.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.281+1666C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159212249 | ||||||
| chr4:159212455
|
G | A | 110 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0025others(107): Show | 110 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.281+1872G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159212455 | ||||||
| chr4:159212463
|
C | A | 26 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0005g0024others(23): Show | 26 | HG00438.hp2 HG00597.hp1 HG01516.hp1 others(23): Show |
intron_variant | MODIFIER | c.281+1880C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159212463 | ||||||
| chr4:159212660
|
TTTAG | T | 2 | a0001c0003t0004g0047a0001c0003t0004g0061 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.281+2081_281+2084d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159212660 | |||||
| chr4:159212676
|
A | G | 2 | a0001c0001t0002g0109a0001c0001t0002g0123 | 2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.281+2093A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159212676 | ||||||
| chr4:159212800
|
A | G | 48 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0071others(45): Show | 48 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.281+2217A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159212800 | ||||||
| chr4:159213374
|
A | C | 107 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0025others(104): Show | 107 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.281+2791A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159213374 | ||||||
| chr4:159213531
|
A | G | 1 | a0001c0002t0001g0107 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.281+2948A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159213531 | ||||||
| chr4:159213538
|
T | G | 1 | a0001c0002t0001g0043 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.281+2955T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159213538 | ||||||
| chr4:159213542
|
A | T | 1 | a0001c0001t0006g0183 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.281+2959A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159213542 | ||||||
| chr4:159213789
|
C | T | 32 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0071others(29): Show | 32 | HG00438.hp2 HG00597.hp1 HG01516.hp1 others(29): Show |
intron_variant | MODIFIER | c.281+3206C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159213789 | ||||||
| chr4:159213826
|
CCACTT | C | 55 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(52): Show | 55 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.281+3246_281+3250d others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159213826 | |||||
| chr4:159213889
|
G | T | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.281+3306G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159213889 | ||||||
| chr4:159213942
|
T | C | 1 | a0001c0002t0003g0176 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.281+3359T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159213942 | ||||||
| chr4:159214069
|
A | G | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.281+3486A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159214069 | ||||||
| chr4:159214107
|
G | T | 55 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(52): Show | 55 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.281+3524G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159214107 | ||||||
| chr4:159214152
|
A | G | 2 | a0001c0001t0002g0109a0001c0001t0002g0123 | 2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.281+3569A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159214152 | ||||||
| chr4:159214163
|
T | C | 2 | a0001c0001t0002g0074a0001c0001t0005g0086 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.281+3580T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159214163 | ||||||
| chr4:159214475
|
G | A | 55 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(52): Show | 55 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.281+3892G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159214475 | ||||||
| chr4:159214484
|
AAC | A | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.281+3903_281+3904d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159214484 | |||||
| chr4:159214771
|
TATG | T | 28 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0004g0194others(25): Show | 28 | HG00438.hp2 HG00597.hp1 HG01516.hp1 others(25): Show |
intron_variant | MODIFIER | c.281+4189_281+4191d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159214771 | ||||||
| chr4:159214904
|
C | T | 4 | a0001c0001t0002g0071a0001c0001t0011g0021a0001c0001t0011g0022others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.281+4321C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159214904 | ||||||
| chr4:159215010
|
C | T | 2 | a0001c0001t0002g0025a0001c0001t0005g0049 | 2 | NA18955.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.281+4427C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159215010 | ||||||
| chr4:159215039
|
T | G | 5 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0002t0001g0027others(2): Show | 5 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.281+4456T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159215039 | ||||||
| chr4:159215144
|
T | C | 1 | a0001c0002t0001g0153 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.281+4561T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159215144 | ||||||
| chr4:159215355
|
G | A | 1 | a0001c0001t0007g0078 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.281+4772G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159215355 | ||||||
| chr4:159215539
|
C | T | 1 | a0001c0002t0003g0189 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.281+4956C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159215539 | ||||||
| chr4:159215556
|
T | G | 48 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0071others(45): Show | 48 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.281+4973T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159215556 | ||||||
| chr4:159215604
|
A | G | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.281+5021A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159215604 | ||||||
| chr4:159215843
|
T | A | 103 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0025others(100): Show | 103 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.281+5260T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159215843 | ||||||
| chr4:159216050
|
G | A | 1 | a0001c0002t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.281+5467G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159216050 | ||||||
| chr4:159216099
|
G | C | 1 | a0001c0001t0002g0109 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.281+5516G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159216099 | ||||||
| chr4:159216228
|
T | G | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.281+5645T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159216228 | ||||||
| chr4:159216252
|
C | T | 2 | a0001c0001t0002g0074a0001c0001t0005g0086 | 2 | HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.281+5669C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159216252 | ||||||
| chr4:159216308
|
C | T | 7 | a0001c0001t0008g0070a0001c0002t0001g0128a0001c0002t0001g0129others(4): Show | 7 | HG00280.hp2 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.281+5725C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159216308 | ||||||
| chr4:159216361
|
T | C | 60 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0071others(57): Show | 60 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.281+5778T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159216361 | ||||||
| chr4:159216392
|
A | G | 45 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(42): Show | 45 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.281+5809A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159216392 | ||||||
| chr4:159216489
|
G | A | 3 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028 | 3 | HG02970.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.281+5906G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159216489 | ||||||
| chr4:159216559
|
A | G | 45 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(42): Show | 45 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.281+5976A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159216559 | ||||||
| chr4:159216746
|
A | G | 1 | a0001c0001t0002g0149 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.281+6163A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159216746 | ||||||
| chr4:159216773
|
C | G | 62 | a0001c0001t0002g0025a0001c0001t0002g0057a0001c0001t0002g0060others(59): Show | 62 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.281+6190C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159216773 | ||||||
| chr4:159216926
|
G | T | 1 | a0001c0002t0003g0176 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.281+6343G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159216926 | ||||||
| chr4:159217091
|
A | G | 3 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028 | 3 | HG02970.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.281+6508A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159217091 | ||||||
| chr4:159217221
|
A | T | 82 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(79): Show | 82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.281+6638A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159217221 | ||||||
| chr4:159217358
|
G | T | 49 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0071others(46): Show | 49 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.281+6775G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159217358 | ||||||
| chr4:159217425
|
T | G | 59 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0071others(56): Show | 59 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.281+6842T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159217425 | ||||||
| chr4:159217508
|
T | C | 3 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0003t0004g0045 | 3 | NA18906.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.281+6925T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159217508 | ||||||
| chr4:159217534
|
C | G | 46 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0071others(43): Show | 46 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.281+6951C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159217534 | ||||||
| chr4:159217809
|
T | G | 141 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(138): Show | 141 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.281+7226T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159217809 | ||||||
| chr4:159217925
|
G | A | 46 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0071others(43): Show | 46 | HG00438.hp2 HG00597.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.281+7342G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159217925 | ||||||
| chr4:159218107
|
C | A | 136 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.281+7524C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159218107 | ||||||
| chr4:159218107
|
C | G | 3 | a0001c0001t0026g0003a0001c0006t0014g0026a0001c0006t0014g0036 | 3 | HG03130.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.281+7524C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159218107 | ||||||
| chr4:159218651
|
G | A | 34 | a0001c0001t0002g0001a0001c0001t0005g0092a0001c0001t0005g0093others(31): Show | 34 | HG00099.hp1 HG00280.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.281+8068G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159218651 | ||||||
| chr4:159218772
|
G | A | 13 | a0001c0001t0002g0029a0001c0001t0002g0088a0001c0001t0002g0090others(10): Show | 13 | HG00280.hp1 HG00639.hp2 HG00738.hp2 others(10): Show |
intron_variant | MODIFIER | c.281+8189G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159218772 | ||||||
| chr4:159218970
|
GT | G | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.281+8389delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159218970 | |||||
| chr4:159219318
|
ACTACAAG | A | 129 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.281+8736_281+8742d others(9): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159219318 | ||||||
| chr4:159219347
|
C | CT | 10 | a0001c0001t0002g0029a0001c0001t0002g0096a0001c0001t0002g0098others(7): Show | 10 | HG00438.hp1 HG00735.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.281+8790dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159219347 | |||||
| chr4:159219347
|
C | CTT | 6 | a0001c0001t0002g0076a0001c0001t0007g0077a0001c0001t0007g0082others(3): Show | 6 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.281+8789_281+8790d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159219347 | |||||
| chr4:159219347
|
CTT | C | 9 | a0001c0001t0008g0033a0001c0001t0008g0041a0001c0001t0011g0021others(6): Show | 9 | HG01496.hp2 HG01934.hp1 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.281+8789_281+8790d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159219347 | |||||
| chr4:159219347
|
CTTT | C | 42 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(39): Show | 42 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.281+8788_281+8790d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159219347 | |||||
| chr4:159219347
|
CTTTT | C | 48 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0005g0012others(45): Show | 48 | HG00438.hp2 HG01069.hp2 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.281+8787_281+8790d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159219347 | |||||
| chr4:159219347
|
CTTTTT | C | 29 | a0001c0001t0002g0001a0001c0001t0006g0163a0001c0001t0006g0170others(26): Show | 29 | HG00099.hp1 HG00280.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.281+8786_281+8790d others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159219347 | |||||
| chr4:159219378
|
C | T | 3 | a0001c0001t0031g0116a0001c0007t0016g0140a0001c0007t0016g0141 | 3 | HG01884.hp1 HG02976.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.281+8795C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159219378 | ||||||
| chr4:159219398
|
C | G | 2 | a0001c0001t0002g0088a0001c0001t0002g0097 | 2 | HG00280.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.281+8815C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159219398 | ||||||
| chr4:159219424
|
G | C | 139 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(136): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.281+8841G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159219424 | ||||||
| chr4:159219424
|
G | T | 2 | a0001c0002t0003g0136a0001c0002t0003g0173 | 2 | HG01123.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.281+8841G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159219424 | ||||||
| chr4:159219495
|
A | G | 32 | a0001c0001t0002g0001a0001c0001t0006g0163a0001c0001t0006g0170others(29): Show | 32 | HG00099.hp1 HG00280.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.281+8912A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159219495 | ||||||
| chr4:159219514
|
T | C | 130 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.281+8931T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159219514 | ||||||
| chr4:159219517
|
G | A | 43 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(40): Show | 43 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.281+8934G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159219517 | ||||||
| chr4:159219581
|
G | A | 48 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0044others(45): Show | 48 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.281+8998G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159219581 | ||||||
| chr4:159219645
|
A | G | 145 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.281+9062A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159219645 | ||||||
| chr4:159219646
|
C | T | 27 | a0001c0001t0002g0005a0001c0001t0002g0025a0001c0001t0002g0060others(24): Show | 27 | HG00438.hp2 HG00597.hp1 HG01516.hp1 others(24): Show |
intron_variant | MODIFIER | c.281+9063C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159219646 | ||||||
| chr4:159219800
|
C | T | 2 | a0001c0001t0004g0193a0001c0003t0004g0045 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.281+9217C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159219800 | ||||||
| chr4:159219910
|
T | G | 5 | a0001c0001t0002g0123a0001c0001t0005g0086a0001c0001t0031g0116others(2): Show | 5 | HG01884.hp1 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.281+9327T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159219910 | ||||||
| chr4:159220033
|
G | A | 58 | a0001c0001t0002g0057a0001c0001t0002g0076a0001c0001t0004g0193others(55): Show | 58 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.281+9450G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159220033 | ||||||
| chr4:159220066
|
T | A | 54 | a0001c0001t0002g0005a0001c0001t0002g0074a0001c0001t0002g0076others(51): Show | 54 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.281+9483T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159220066 | ||||||
| chr4:159220782
|
C | T | 11 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0008g0070others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.281+10199C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159220782 | ||||||
| chr4:159220824
|
A | G | 65 | a0001c0001t0002g0010a0001c0001t0002g0044a0001c0001t0002g0071others(62): Show | 65 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.281+10241A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159220824 | ||||||
| chr4:159220859
|
A | C | 59 | a0001c0001t0002g0010a0001c0001t0002g0044a0001c0001t0002g0071others(56): Show | 59 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.281+10276A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159220859 | ||||||
| chr4:159221003
|
T | G | 7 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0001t0008g0112others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.281+10420T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159221003 | ||||||
| chr4:159221051
|
C | T | 65 | a0001c0001t0002g0010a0001c0001t0002g0044a0001c0001t0002g0071others(62): Show | 65 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.281+10468C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159221051 | ||||||
| chr4:159221320
|
A | G | 2 | a0001c0001t0009g0058a0001c0001t0009g0059 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.281+10737A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159221320 | ||||||
| chr4:159221458
|
C | A | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.281+10875C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159221458 | ||||||
| chr4:159221498
|
A | G | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.281+10915A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159221498 | ||||||
| chr4:159221556
|
A | G | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.281+10973A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159221556 | ||||||
| chr4:159221708
|
C | T | 25 | a0001c0001t0004g0193a0001c0001t0006g0170a0001c0001t0006g0183others(22): Show | 25 | HG00099.hp1 HG00738.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.281+11125C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159221708 | ||||||
| chr4:159221833
|
A | C | 1 | a0001c0001t0002g0124 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.281+11250A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159221833 | ||||||
| chr4:159222032
|
G | A | 1 | a0001c0002t0003g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.281+11449G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159222032 | ||||||
| chr4:159222193
|
C | T | 1 | a0001c0001t0031g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.281+11610C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159222193 | ||||||
| chr4:159222463
|
G | T | 58 | a0001c0001t0002g0010a0001c0001t0002g0044a0001c0001t0002g0071others(55): Show | 58 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.281+11880G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159222463 | ||||||
| chr4:159222499
|
A | G | 1 | a0001c0001t0002g0145 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.281+11916A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159222499 | ||||||
| chr4:159222505
|
C | T | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.281+11922C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159222505 | ||||||
| chr4:159222527
|
A | C | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.281+11944A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159222527 | ||||||
| chr4:159222568
|
C | T | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.281+11985C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159222568 | ||||||
| chr4:159222874
|
C | G | 1 | a0001c0001t0006g0183 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.281+12291C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159222874 | ||||||
| chr4:159222884
|
A | T | 3 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028 | 3 | HG02970.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.281+12301A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159222884 | ||||||
| chr4:159222916
|
T | TTA | 44 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0029others(41): Show | 44 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.281+12351_281+1235 others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159222916 | |||||
| chr4:159222916
|
TTATA | T | 67 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.281+12349_281+1235 others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159222916 | |||||
| chr4:159223052
|
G | A | 67 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.281+12469G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159223052 | ||||||
| chr4:159223144
|
T | G | 1 | a0001c0002t0003g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.281+12561T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159223144 | ||||||
| chr4:159223206
|
T | TCTTA | 130 | a0001c0001t0002g0010a0001c0001t0002g0025a0001c0001t0002g0044others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.281+12625_281+1262 others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159223206 | |||||
| chr4:159223215
|
G | A | 24 | a0001c0001t0005g0024a0001c0001t0005g0092a0001c0001t0005g0093others(21): Show | 24 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.281+12632G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159223215 | ||||||
| chr4:159223276
|
C | T | 1 | a0001c0002t0001g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.281+12693C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159223276 | ||||||
| chr4:159223296
|
C | A | 24 | a0001c0001t0005g0024a0001c0001t0005g0092a0001c0001t0005g0093others(21): Show | 24 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.281+12713C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159223296 | ||||||
| chr4:159223312
|
G | A | 1 | a0001c0002t0001g0018 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.281+12729G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159223312 | ||||||
| chr4:159223342
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.281+12759T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159223342 | ||||||
| chr4:159223512
|
A | G | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.281+12929A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159223512 | ||||||
| chr4:159223543
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.281+12960G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159223543 | ||||||
| chr4:159223629
|
A | G | 2 | a0001c0001t0033g0113a0001c0001t0034g0115 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.281+13046A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159223629 | ||||||
| chr4:159223688
|
C | T | 67 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.281+13105C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159223688 | ||||||
| chr4:159223710
|
G | C | 67 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.281+13127G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159223710 | ||||||
| chr4:159223904
|
T | G | 1 | a0001c0002t0003g0169 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.281+13321T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159223904 | ||||||
| chr4:159223968
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.281+13385G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159223968 | ||||||
| chr4:159224060
|
G | A | 1 | a0001c0002t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.281+13477G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159224060 | ||||||
| chr4:159224240
|
T | G | 1 | a0001c0003t0017g0117 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.281+13657T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159224240 | ||||||
| chr4:159224306
|
A | G | 12 | a0001c0002t0018g0148a0001c0003t0004g0009a0001c0003t0004g0045others(9): Show | 12 | HG00735.hp1 HG01081.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.281+13723A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159224306 | ||||||
| chr4:159224548
|
A | G | 3 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028 | 3 | HG02970.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.281+13965A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159224548 | ||||||
| chr4:159224666
|
A | T | 1 | a0001c0001t0010g0162 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.281+14083A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159224666 | ||||||
| chr4:159225045
|
G | A | 41 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(38): Show | 41 | HG00099.hp1 HG00438.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.282-13764G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159225045 | ||||||
| chr4:159225193
|
T | C | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.282-13616T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159225193 | ||||||
| chr4:159225515
|
A | G | 1 | a0001c0002t0001g0139 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.282-13294A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159225515 | ||||||
| chr4:159225724
|
T | A | 41 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(38): Show | 41 | HG00099.hp1 HG00438.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.282-13085T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159225724 | ||||||
| chr4:159225927
|
T | G | 1 | a0001c0001t0002g0121 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.282-12882T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159225927 | ||||||
| chr4:159226007
|
C | T | 61 | a0001c0001t0002g0010a0001c0001t0002g0044a0001c0001t0002g0071others(58): Show | 61 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.282-12802C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159226007 | ||||||
| chr4:159226250
|
T | A | 6 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0001t0008g0112others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.282-12559T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159226250 | ||||||
| chr4:159226259
|
C | T | 1 | a0001c0001t0028g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.282-12550C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159226259 | ||||||
| chr4:159226643
|
G | A | 41 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(38): Show | 41 | HG00099.hp1 HG00438.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.282-12166G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159226643 | ||||||
| chr4:159226778
|
G | T | 2 | a0001c0002t0003g0160a0001c0002t0003g0166 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.282-12031G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159226778 | ||||||
| chr4:159226866
|
G | A | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.282-11943G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159226866 | ||||||
| chr4:159226950
|
G | A | 1 | a0001c0001t0007g0078 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.282-11859G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159226950 | ||||||
| chr4:159227343
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.282-11466A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159227343 | ||||||
| chr4:159227355
|
G | T | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.282-11454G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159227355 | ||||||
| chr4:159228023
|
G | A | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.282-10786G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159228023 | ||||||
| chr4:159228340
|
A | T | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.282-10469A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159228340 | ||||||
| chr4:159228669
|
A | G | 41 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(38): Show | 41 | HG00099.hp1 HG00438.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.282-10140A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159228669 | ||||||
| chr4:159228675
|
A | G | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.282-10134A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159228675 | ||||||
| chr4:159228723
|
C | T | 67 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.282-10086C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159228723 | ||||||
| chr4:159229331
|
G | A | 7 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0001t0008g0112others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.282-9478G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159229331 | ||||||
| chr4:159229457
|
G | A | 41 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(38): Show | 41 | HG00099.hp1 HG00438.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.282-9352G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159229457 | ||||||
| chr4:159229730
|
T | C | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.282-9079T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159229730 | ||||||
| chr4:159229788
|
T | C | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.282-9021T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159229788 | ||||||
| chr4:159229984
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.282-8825G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159229984 | ||||||
| chr4:159230024
|
G | A | 129 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.282-8785G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159230024 | ||||||
| chr4:159230130
|
G | A | 1 | a0001c0001t0007g0082 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.282-8679G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159230130 | ||||||
| chr4:159230159
|
A | T | 1 | a0001c0002t0001g0052 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.282-8650A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159230159 | ||||||
| chr4:159230172
|
C | G | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.282-8637C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159230172 | ||||||
| chr4:159230696
|
C | T | 1 | a0001c0002t0018g0148 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.282-8113C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159230696 | ||||||
| chr4:159230774
|
C | T | 1 | a0001c0001t0009g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.282-8035C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159230774 | ||||||
| chr4:159230841
|
T | C | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.282-7968T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159230841 | ||||||
| chr4:159231413
|
A | G | 63 | a0001c0001t0002g0010a0001c0001t0002g0044a0001c0001t0002g0071others(60): Show | 63 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.282-7396A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159231413 | ||||||
| chr4:159231422
|
A | G | 2 | a0001c0001t0002g0109a0001c0001t0002g0123 | 2 | HG02809.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.282-7387A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159231422 | ||||||
| chr4:159231593
|
G | T | 2 | a0001c0002t0001g0027a0001c0002t0001g0038 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.282-7216G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159231593 | ||||||
| chr4:159231990
|
G | C | 1 | a0001c0001t0007g0082 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.282-6819G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159231990 | ||||||
| chr4:159232066
|
C | T | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.282-6743C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159232066 | ||||||
| chr4:159232069
|
G | A | 127 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.282-6740G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159232069 | ||||||
| chr4:159232123
|
T | C | 1 | a0001c0001t0006g0170 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.282-6686T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159232123 | ||||||
| chr4:159232256
|
G | C | 1 | a0001c0002t0003g0166 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.282-6553G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159232256 | ||||||
| chr4:159232289
|
C | T | 42 | a0001c0001t0002g0044a0001c0001t0002g0071a0001c0001t0008g0033others(39): Show | 42 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.282-6520C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159232289 | ||||||
| chr4:159232401
|
G | A | 16 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028others(13): Show | 16 | HG00735.hp1 HG01081.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.282-6408G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159232401 | ||||||
| chr4:159232637
|
G | T | 3 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0003g0186 | 3 | HG01516.hp2 HG01517.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.282-6172G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159232637 | ||||||
| chr4:159232787
|
T | C | 1 | a0001c0001t0028g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.282-6022T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159232787 | ||||||
| chr4:159232807
|
A | G | 16 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028others(13): Show | 16 | HG00735.hp1 HG01081.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.282-6002A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159232807 | ||||||
| chr4:159232859
|
G | C | 16 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028others(13): Show | 16 | HG00735.hp1 HG01081.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.282-5950G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159232859 | ||||||
| chr4:159233246
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.282-5563G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159233246 | ||||||
| chr4:159233637
|
G | A | 7 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0001t0008g0112others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.282-5172G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159233637 | ||||||
| chr4:159233726
|
T | C | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.282-5083T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159233726 | ||||||
| chr4:159233832
|
A | G | 7 | a0001c0001t0009g0035a0001c0001t0010g0155a0001c0001t0010g0162others(4): Show | 7 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.282-4977A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159233832 | ||||||
| chr4:159233944
|
CG | C | 37 | a0001c0001t0002g0044a0001c0001t0008g0033a0001c0001t0008g0041others(34): Show | 37 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.282-4864delG | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159233944 | ||||||
| chr4:159233945
|
G | A | 9 | a0001c0001t0005g0086a0001c0001t0007g0077a0001c0001t0007g0078others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.282-4864G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159233945 | ||||||
| chr4:159233960
|
T | A | 1 | a0001c0003t0004g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.282-4849T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159233960 | ||||||
| chr4:159234016
|
A | G | 2 | a0001c0001t0009g0035a0001c0001t0029g0002 | 2 | HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.282-4793A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159234016 | ||||||
| chr4:159234100
|
TTATTA | T | 7 | a0001c0001t0009g0035a0001c0001t0010g0155a0001c0001t0010g0162others(4): Show | 7 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.282-4706_282-4702d others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159234100 | |||||
| chr4:159234369
|
TA | T | 67 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.282-4438delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159234369 | |||||
| chr4:159234436
|
GTAGTGGA others(5): Show |
G | 1 | a0001c0001t0005g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.282-4372_282-4361d others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159234436 | ||||||
| chr4:159234445
|
C | T | 8 | a0001c0001t0005g0024a0001c0001t0008g0062a0001c0001t0008g0067others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.282-4364C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159234445 | ||||||
| chr4:159234549
|
A | AT | 9 | a0001c0001t0002g0005a0001c0001t0002g0066a0001c0001t0002g0076others(6): Show | 9 | HG00438.hp1 HG01109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.282-4236dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159234549 | |||||
| chr4:159234549
|
ATTT | A | 87 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0071others(84): Show | 87 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.282-4238_282-4236d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159234549 | |||||
| chr4:159234549
|
ATTTT | A | 39 | a0001c0001t0002g0044a0001c0001t0006g0183a0001c0001t0008g0033others(36): Show | 39 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.282-4239_282-4236d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159234549 | |||||
| chr4:159234549
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0002g0015 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.282-4246_282-4236d others(13): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159234549 | |||||
| chr4:159234561
|
T | C | 1 | a0001c0002t0001g0018 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.282-4248T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159234561 | ||||||
| chr4:159234594
|
C | T | 62 | a0001c0001t0002g0044a0001c0001t0002g0071a0001c0001t0005g0086others(59): Show | 62 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.282-4215C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159234594 | ||||||
| chr4:159234760
|
C | A | 3 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028 | 3 | HG02970.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.282-4049C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159234760 | ||||||
| chr4:159235079
|
C | T | 129 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.282-3730C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159235079 | ||||||
| chr4:159235090
|
G | A | 38 | a0001c0001t0002g0044a0001c0001t0008g0033a0001c0001t0008g0041others(35): Show | 38 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.282-3719G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159235090 | ||||||
| chr4:159235176
|
G | T | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.282-3633G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159235176 | ||||||
| chr4:159235341
|
TTAA | T | 3 | a0001c0001t0009g0058a0001c0001t0009g0059a0001c0002t0003g0168 | 3 | HG01981.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.282-3464_282-3462d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159235341 | |||||
| chr4:159235456
|
C | T | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.282-3353C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159235456 | ||||||
| chr4:159235475
|
C | T | 3 | a0001c0002t0018g0148a0001c0003t0017g0117a0001c0003t0019g0135 | 3 | HG00735.hp1 HG01081.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.282-3334C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159235475 | ||||||
| chr4:159235681
|
C | T | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.282-3128C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159235681 | ||||||
| chr4:159235685
|
A | G | 1 | a0001c0001t0028g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.282-3124A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159235685 | ||||||
| chr4:159235718
|
T | C | 2 | a0001c0001t0002g0103a0001c0001t0002g0124 | 2 | HG00642.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.282-3091T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159235718 | ||||||
| chr4:159235891
|
T | C | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.282-2918T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159235891 | ||||||
| chr4:159235967
|
C | T | 1 | a0001c0001t0002g0010 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.282-2842C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159235967 | ||||||
| chr4:159236375
|
G | A | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.282-2434G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159236375 | ||||||
| chr4:159236490
|
T | C | 127 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.282-2319T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159236490 | ||||||
| chr4:159236622
|
A | T | 1 | a0001c0002t0001g0158 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.282-2187A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159236622 | ||||||
| chr4:159236642
|
CA | C | 62 | a0001c0001t0002g0044a0001c0001t0002g0071a0001c0001t0005g0086others(59): Show | 62 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.282-2165delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159236642 | |||||
| chr4:159236646
|
T | C | 62 | a0001c0001t0002g0044a0001c0001t0002g0071a0001c0001t0005g0086others(59): Show | 62 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.282-2163T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159236646 | ||||||
| chr4:159236774
|
G | A | 6 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0001t0008g0112others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.282-2035G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159236774 | ||||||
| chr4:159236869
|
T | C | 1 | a0001c0002t0003g0181 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.282-1940T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159236869 | ||||||
| chr4:159236921
|
G | A | 1 | a0001c0002t0003g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.282-1888G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159236921 | ||||||
| chr4:159236988
|
T | C | 7 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0001t0008g0112others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.282-1821T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159236988 | ||||||
| chr4:159237118
|
T | C | 1 | a0001c0001t0002g0131 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.282-1691T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159237118 | ||||||
| chr4:159237240
|
C | T | 7 | a0001c0001t0009g0035a0001c0001t0010g0155a0001c0001t0010g0162others(4): Show | 7 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.282-1569C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159237240 | ||||||
| chr4:159237348
|
T | A | 9 | a0001c0001t0005g0086a0001c0001t0007g0077a0001c0001t0007g0078others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.282-1461T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159237348 | ||||||
| chr4:159237571
|
G | C | 62 | a0001c0001t0002g0044a0001c0001t0002g0071a0001c0001t0005g0086others(59): Show | 62 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.282-1238G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159237571 | ||||||
| chr4:159237842
|
T | TA | 21 | a0001c0001t0002g0029a0001c0001t0002g0057a0001c0001t0002g0101others(18): Show | 21 | HG00438.hp1 HG00735.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-938dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159237842 | |||||
| chr4:159237842
|
TA | T | 15 | a0001c0001t0002g0125a0001c0001t0002g0149a0001c0001t0005g0012others(12): Show | 15 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.282-938delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159237842 | |||||
| chr4:159237842
|
TAA | T | 14 | a0001c0001t0002g0071a0001c0001t0004g0194a0001c0001t0009g0035others(11): Show | 14 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.282-939_282-938del others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159237842 | |||||
| chr4:159237842
|
TAAA | T | 6 | a0001c0002t0001g0040a0001c0002t0001g0052a0001c0002t0001g0053others(3): Show | 6 | HG00597.hp1 HG00733.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.282-940_282-938del others(3): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159237842 | |||||
| chr4:159237842
|
TAAAA | T | 30 | a0001c0001t0008g0033a0001c0001t0008g0041a0001c0001t0028g0167others(27): Show | 30 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.282-941_282-938del others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159237842 | |||||
| chr4:159237842
|
TAAAAAAA | T | 39 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(36): Show | 39 | HG00099.hp1 HG00438.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.282-944_282-938del others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159237842 | |||||
| chr4:159237842
|
TAAAAAAA others(3): Show |
T | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.282-947_282-938del others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159237842 | |||||
| chr4:159237842
|
TAAAAAAA others(6): Show |
T | 9 | a0001c0001t0005g0086a0001c0001t0007g0077a0001c0001t0007g0078others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.282-950_282-938del others(13): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr4 | 159237842 | |||||
| chr4:159237843
|
A | T | 1 | a0001c0001t0002g0130 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.282-966A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159237843 | ||||||
| chr4:159238095
|
C | A | 1 | a0001c0001t0005g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.282-714C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159238095 | ||||||
| chr4:159238753
|
A | G | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.282-56A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159238753 | ||||||
| chr4:159238797
|
C | A | 5 | a0001c0001t0006g0175a0001c0001t0006g0177a0001c0001t0015g0190others(2): Show | 5 | HG01099.hp2 HG01891.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.282-12C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 4/29 | chr4 | 159238797 | ||||||
| chr4:159239046
|
TGA | T | 16 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028others(13): Show | 16 | HG00735.hp1 HG01081.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.357+164_357+165del others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr4 | 159239046 | |||||
| chr4:159239119
|
T | G | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.357+235T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | chr4 | 159239119 | ||||||
| chr4:159239363
|
T | C | 67 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.357+479T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | chr4 | 159239363 | ||||||
| chr4:159239516
|
T | G | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.357+632T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | chr4 | 159239516 | ||||||
| chr4:159239592
|
A | G | 6 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0001t0008g0112others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.357+708A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | chr4 | 159239592 | ||||||
| chr4:159239794
|
T | G | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.357+910T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | chr4 | 159239794 | ||||||
| chr4:159239810
|
T | TAAATAAA others(334): Show |
2 | a0001c0003t0004g0047a0001c0003t0004g0061 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.357+940_357+941ins others(341): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr4 | 159239810 | |||||
| chr4:159239905
|
C | T | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.357+1021C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | chr4 | 159239905 | ||||||
| chr4:159240172
|
T | C | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.358-1029T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | chr4 | 159240172 | ||||||
| chr4:159240233
|
G | T | 1 | a0001c0001t0005g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.358-968G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | chr4 | 159240233 | ||||||
| chr4:159240331
|
C | CTTTTT | 115 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.358-855_358-851dup others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr4 | 159240331 | |||||
| chr4:159240331
|
C | CTTTTTT | 54 | a0001c0001t0002g0010a0001c0001t0004g0193a0001c0001t0005g0012others(51): Show | 54 | HG00642.hp2 HG00735.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.358-856_358-851dup others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr4 | 159240331 | |||||
| chr4:159240331
|
C | CTTTTTTT | 8 | a0001c0001t0002g0025a0001c0001t0005g0092a0001c0001t0005g0093others(5): Show | 8 | HG02615.hp1 HG02809.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.358-857_358-851dup others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr4 | 159240331 | |||||
| chr4:159240331
|
C | CTTTTTTT others(3): Show |
1 | a0001c0006t0014g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.358-860_358-851dup others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr4 | 159240331 | |||||
| chr4:159240331
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0007g0094a0001c0001t0007g0095a0001c0001t0023g0073others(1): Show | 4 | HG01123.hp1 HG02451.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.358-861_358-851dup others(11): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr4 | 159240331 | |||||
| chr4:159240331
|
C | CTTTTTTT others(5): Show |
4 | a0001c0001t0007g0077a0001c0001t0007g0082a0001c0001t0007g0127others(1): Show | 4 | HG01891.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.358-862_358-851dup others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr4 | 159240331 | |||||
| chr4:159240331
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0007g0078 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.358-863_358-851dup others(13): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr4 | 159240331 | |||||
| chr4:159240331
|
C | CTTTTTTT others(8): Show |
1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.358-865_358-851dup others(15): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr4 | 159240331 | |||||
| chr4:159240356
|
C | T | 41 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(38): Show | 41 | HG00099.hp1 HG00438.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.358-845C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | chr4 | 159240356 | ||||||
| chr4:159240668
|
A | G | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.358-533A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | chr4 | 159240668 | ||||||
| chr4:159240764
|
T | C | 75 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.358-437T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | chr4 | 159240764 | ||||||
| chr4:159240807
|
G | GT | 7 | a0001c0001t0002g0131a0001c0001t0006g0175a0001c0001t0008g0041others(4): Show | 7 | HG00099.hp2 HG02074.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.358-375dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr4 | 159240807 | |||||
| chr4:159240807
|
GTT | G | 10 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0001t0008g0112others(7): Show | 10 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.358-376_358-375del others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr4 | 159240807 | |||||
| chr4:159240807
|
GTTT | G | 24 | a0001c0001t0005g0024a0001c0001t0005g0092a0001c0001t0005g0093others(21): Show | 24 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.358-377_358-375del others(3): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr4 | 159240807 | |||||
| chr4:159241072
|
T | C | 1 | a0001c0002t0001g0100 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.358-129T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | chr4 | 159241072 | ||||||
| chr4:159241146
|
A | G | 41 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(38): Show | 41 | HG00099.hp1 HG00438.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.358-55A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | chr4 | 159241146 | ||||||
| chr4:159241163
|
T | C | 130 | a0001c0001t0002g0010a0001c0001t0002g0025a0001c0001t0002g0044others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.358-38T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 5/29 | chr4 | 159241163 | ||||||
| chr4:159241446
|
C | A | 1 | a0001c0001t0002g0096 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.525+78C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159241446 | ||||||
| chr4:159241474
|
A | G | 1 | a0001c0001t0002g0149 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.525+106A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159241474 | ||||||
| chr4:159241484
|
A | G | 1 | a0001c0002t0001g0037 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.525+116A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159241484 | ||||||
| chr4:159241517
|
T | G | 6 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0001t0008g0112others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.525+149T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159241517 | ||||||
| chr4:159241973
|
C | A | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+605C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159241973 | ||||||
| chr4:159241992
|
G | C | 16 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028others(13): Show | 16 | HG00735.hp1 HG01081.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.525+624G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159241992 | ||||||
| chr4:159242147
|
C | CT | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.525+787dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr4 | 159242147 | |||||
| chr4:159242186
|
C | T | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.525+818C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159242186 | ||||||
| chr4:159242365
|
T | G | 1 | a0001c0001t0002g0118 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.525+997T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159242365 | ||||||
| chr4:159242452
|
ATATATCT | A | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.525+1089_525+1095d others(9): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr4 | 159242452 | |||||
| chr4:159242718
|
T | TA | 130 | a0001c0001t0002g0010a0001c0001t0002g0025a0001c0001t0002g0044others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.526-1050dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr4 | 159242718 | |||||
| chr4:159242801
|
A | G | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-973A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159242801 | ||||||
| chr4:159242924
|
G | A | 8 | a0001c0003t0004g0009a0001c0003t0004g0047a0001c0003t0004g0061others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.526-850G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159242924 | ||||||
| chr4:159242925
|
C | T | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.526-849C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159242925 | ||||||
| chr4:159242926
|
G | A | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.526-848G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159242926 | ||||||
| chr4:159242971
|
T | C | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.526-803T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159242971 | ||||||
| chr4:159243017
|
C | T | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.526-757C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159243017 | ||||||
| chr4:159243113
|
G | GT | 10 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0001t0008g0112others(7): Show | 10 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.526-649dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr4 | 159243113 | |||||
| chr4:159243113
|
GT | G | 24 | a0001c0001t0002g0091a0001c0001t0005g0012a0001c0001t0005g0051others(21): Show | 24 | HG01123.hp1 HG01496.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.526-649delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr4 | 159243113 | |||||
| chr4:159243248
|
G | A | 1 | a0001c0003t0004g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.526-526G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159243248 | ||||||
| chr4:159243384
|
T | C | 1 | a0001c0002t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.526-390T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159243384 | ||||||
| chr4:159243462
|
C | T | 128 | a0001c0001t0002g0010a0001c0001t0002g0025a0001c0001t0002g0044others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.526-312C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159243462 | ||||||
| chr4:159243590
|
C | T | 1 | a0001c0002t0001g0075 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.526-184C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159243590 | ||||||
| chr4:159243620
|
C | T | 1 | a0001c0002t0003g0176 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.526-154C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | chr4 | 159243620 | ||||||
| chr4:159243667
|
CT | C | 9 | a0001c0001t0005g0024a0001c0001t0007g0077a0001c0001t0007g0078others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.526-105delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr4 | 159243667 | |||||
| chr4:159244073
|
C | T | 89 | a0001c0001t0002g0044a0001c0001t0002g0071a0001c0001t0004g0194others(86): Show | 89 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.543+282C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159244073 | ||||||
| chr4:159244544
|
G | A | 6 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0001t0008g0112others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+753G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159244544 | ||||||
| chr4:159244698
|
A | T | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543+907A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159244698 | ||||||
| chr4:159244955
|
C | T | 129 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.543+1164C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159244955 | ||||||
| chr4:159245011
|
T | C | 1 | a0001c0002t0003g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.543+1220T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159245011 | ||||||
| chr4:159245111
|
C | T | 129 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.543+1320C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159245111 | ||||||
| chr4:159245199
|
T | C | 186 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(183): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.543+1408T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159245199 | ||||||
| chr4:159245210
|
A | C | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543+1419A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159245210 | ||||||
| chr4:159245561
|
C | T | 2 | a0001c0001t0005g0092a0001c0001t0005g0093 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.543+1770C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159245561 | ||||||
| chr4:159245824
|
A | AAC | 9 | a0001c0001t0005g0024a0001c0001t0007g0077a0001c0001t0007g0078others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+2034_543+2035i others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159245824 | |||||
| chr4:159245826
|
A | G | 9 | a0001c0001t0005g0024a0001c0001t0007g0077a0001c0001t0007g0078others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+2035A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159245826 | ||||||
| chr4:159245834
|
C | T | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.543+2043C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159245834 | ||||||
| chr4:159245987
|
A | C | 75 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.543+2196A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159245987 | ||||||
| chr4:159246046
|
A | G | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.543+2255A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159246046 | ||||||
| chr4:159246054
|
C | T | 75 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.543+2263C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159246054 | ||||||
| chr4:159246156
|
G | A | 129 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.543+2365G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159246156 | ||||||
| chr4:159246170
|
T | C | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.543+2379T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159246170 | ||||||
| chr4:159246486
|
G | T | 1 | a0001c0001t0002g0132 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.543+2695G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159246486 | ||||||
| chr4:159246536
|
G | A | 75 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.543+2745G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159246536 | ||||||
| chr4:159246757
|
T | C | 75 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.543+2966T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159246757 | ||||||
| chr4:159246778
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.543+2987A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159246778 | ||||||
| chr4:159246859
|
T | C | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.543+3068T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159246859 | ||||||
| chr4:159246860
|
G | A | 1 | a0001c0002t0003g0169 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.543+3069G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159246860 | ||||||
| chr4:159247107
|
T | C | 57 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(54): Show | 57 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.543+3316T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159247107 | ||||||
| chr4:159247440
|
A | T | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.543+3649A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159247440 | ||||||
| chr4:159247499
|
T | C | 1 | a0001c0001t0002g0090 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.543+3708T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159247499 | ||||||
| chr4:159247549
|
G | A | 1 | a0001c0001t0020g0120 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.543+3758G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159247549 | ||||||
| chr4:159247755
|
C | CT | 29 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0066others(26): Show | 29 | HG00558.hp1 HG00642.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.543+3989dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159247755 | |||||
| chr4:159247755
|
C | CTT | 9 | a0001c0001t0002g0132a0001c0001t0005g0086a0001c0001t0006g0187others(6): Show | 9 | HG00597.hp2 HG02055.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+3988_543+3989d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159247755 | |||||
| chr4:159247755
|
C | CTTT | 6 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(3): Show | 6 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+3987_543+3989d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159247755 | |||||
| chr4:159247755
|
CT | C | 58 | a0001c0001t0002g0044a0001c0001t0002g0071a0001c0001t0005g0024others(55): Show | 58 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.543+3989delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159247755 | |||||
| chr4:159247755
|
CTT | C | 9 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0009g0035others(6): Show | 9 | HG00597.hp1 HG01978.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.543+3988_543+3989d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159247755 | |||||
| chr4:159247755
|
CTTT | C | 27 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0004g0193others(24): Show | 27 | HG00099.hp1 HG00438.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.543+3987_543+3989d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159247755 | |||||
| chr4:159247755
|
CTTTT | C | 12 | a0001c0001t0002g0079a0001c0001t0004g0194a0001c0001t0009g0058others(9): Show | 12 | HG00738.hp1 HG00738.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.543+3986_543+3989d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159247755 | |||||
| chr4:159247755
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0008g0033a0001c0001t0008g0041 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.543+3977_543+3989d others(15): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159247755 | |||||
| chr4:159247953
|
G | A | 2 | a0001c0001t0008g0033a0001c0001t0008g0041 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.543+4162G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159247953 | ||||||
| chr4:159247982
|
G | C | 1 | a0001c0003t0004g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.543+4191G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159247982 | ||||||
| chr4:159248000
|
G | T | 1 | a0001c0001t0002g0096 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.543+4209G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159248000 | ||||||
| chr4:159248220
|
C | G | 54 | a0001c0001t0002g0010a0001c0001t0002g0044a0001c0001t0002g0071others(51): Show | 54 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.543+4429C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159248220 | ||||||
| chr4:159248319
|
A | G | 1 | a0001c0001t0028g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.543+4528A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159248319 | ||||||
| chr4:159248326
|
T | C | 5 | a0001c0003t0004g0009a0001c0003t0004g0047a0001c0003t0004g0061others(2): Show | 5 | HG02109.hp2 HG02145.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+4535T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159248326 | ||||||
| chr4:159248366
|
A | G | 1 | a0001c0001t0028g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.543+4575A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159248366 | ||||||
| chr4:159248568
|
T | C | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.543+4777T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159248568 | ||||||
| chr4:159248719
|
T | C | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.543+4928T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159248719 | ||||||
| chr4:159249077
|
A | G | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.543+5286A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159249077 | ||||||
| chr4:159249203
|
C | T | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.543+5412C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159249203 | ||||||
| chr4:159249228
|
A | ATT | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+5447_543+5448d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159249228 | |||||
| chr4:159249228
|
AT | A | 15 | a0001c0001t0026g0003a0001c0002t0018g0148a0001c0003t0004g0009others(12): Show | 15 | HG00735.hp1 HG01081.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.543+5448delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159249228 | |||||
| chr4:159249283
|
CTCTT | C | 7 | a0001c0001t0009g0035a0001c0001t0010g0155a0001c0001t0010g0162others(4): Show | 7 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+5494_543+5497d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159249283 | |||||
| chr4:159249285
|
C | CT | 19 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0006g0175others(16): Show | 19 | HG00280.hp2 HG01934.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.543+5511dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159249285 | |||||
| chr4:159249285
|
CT | C | 34 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0066others(31): Show | 34 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.543+5511delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159249285 | |||||
| chr4:159249285
|
CTT | C | 29 | a0001c0001t0002g0060a0001c0001t0002g0079a0001c0001t0004g0193others(26): Show | 29 | HG00438.hp2 HG00738.hp1 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.543+5510_543+5511d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159249285 | |||||
| chr4:159249392
|
C | A | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.543+5601C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159249392 | ||||||
| chr4:159249452
|
CATT | C | 6 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0001t0008g0112others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+5666_543+5668d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159249452 | |||||
| chr4:159249509
|
A | G | 43 | a0001c0001t0002g0010a0001c0001t0002g0044a0001c0001t0002g0071others(40): Show | 43 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.543+5718A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159249509 | ||||||
| chr4:159249619
|
C | T | 41 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(38): Show | 41 | HG00099.hp1 HG00438.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.543+5828C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159249619 | ||||||
| chr4:159249699
|
C | CT | 34 | a0001c0001t0005g0024a0001c0001t0005g0092a0001c0001t0005g0093others(31): Show | 34 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.543+5917dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159249699 | |||||
| chr4:159249915
|
C | T | 1 | a0002c0009t0002g0011 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.543+6124C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159249915 | ||||||
| chr4:159250092
|
C | A | 16 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028others(13): Show | 16 | HG00735.hp1 HG01081.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.543+6301C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159250092 | ||||||
| chr4:159250124
|
T | G | 1 | a0001c0001t0002g0044 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.543+6333T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159250124 | ||||||
| chr4:159250229
|
G | A | 3 | a0001c0002t0001g0040a0001c0002t0001g0054a0001c0002t0001g0055 | 3 | HG00733.hp1 HG01109.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.543+6438G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159250229 | ||||||
| chr4:159250301
|
C | T | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.543+6510C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159250301 | ||||||
| chr4:159250357
|
A | G | 54 | a0001c0001t0002g0044a0001c0001t0002g0071a0001c0001t0005g0086others(51): Show | 54 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.543+6566A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159250357 | ||||||
| chr4:159250506
|
C | T | 41 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(38): Show | 41 | HG00099.hp1 HG00438.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.543+6715C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159250506 | ||||||
| chr4:159250665
|
C | CTT | 6 | a0001c0001t0008g0062a0001c0001t0008g0112a0001c0001t0027g0104others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+6894_543+6895d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159250665 | |||||
| chr4:159250665
|
C | CTTT | 12 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0007g0078others(9): Show | 12 | HG01123.hp1 HG01891.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.543+6893_543+6895d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159250665 | |||||
| chr4:159250665
|
C | CTTTT | 11 | a0001c0001t0007g0077a0001c0003t0004g0009a0001c0003t0004g0045others(8): Show | 11 | HG01081.hp2 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.543+6892_543+6895d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159250665 | |||||
| chr4:159250665
|
CTT | C | 50 | a0001c0001t0002g0044a0001c0001t0002g0071a0001c0001t0005g0086others(47): Show | 50 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.543+6894_543+6895d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159250665 | |||||
| chr4:159250665
|
CTTTT | C | 37 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(34): Show | 37 | HG00099.hp1 HG00438.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.543+6892_543+6895d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159250665 | |||||
| chr4:159250665
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.543+6885_543+6895d others(13): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159250665 | |||||
| chr4:159250732
|
G | A | 2 | a0001c0003t0017g0117a0001c0003t0019g0135 | 2 | HG01081.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.543+6941G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159250732 | ||||||
| chr4:159250765
|
A | G | 4 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0164others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+6974A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159250765 | ||||||
| chr4:159250793
|
G | C | 75 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.543+7002G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159250793 | ||||||
| chr4:159250794
|
C | T | 75 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.543+7003C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159250794 | ||||||
| chr4:159250852
|
C | T | 9 | a0001c0001t0005g0024a0001c0001t0007g0077a0001c0001t0007g0078others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+7061C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159250852 | ||||||
| chr4:159251063
|
T | C | 75 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.543+7272T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159251063 | ||||||
| chr4:159251087
|
G | A | 3 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028 | 3 | HG02970.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.543+7296G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159251087 | ||||||
| chr4:159251166
|
C | G | 4 | a0001c0001t0002g0071a0001c0001t0011g0021a0001c0001t0011g0022others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+7375C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159251166 | ||||||
| chr4:159251167
|
C | G | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.543+7376C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159251167 | ||||||
| chr4:159251226
|
G | A | 1 | a0001c0001t0006g0163 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.543+7435G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159251226 | ||||||
| chr4:159251255
|
G | A | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.543+7464G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159251255 | ||||||
| chr4:159251279
|
G | A | 1 | a0001c0002t0003g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.543+7488G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159251279 | ||||||
| chr4:159251339
|
T | C | 75 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.543+7548T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159251339 | ||||||
| chr4:159251488
|
G | C | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+7697G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159251488 | ||||||
| chr4:159251735
|
G | A | 1 | a0001c0001t0011g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.543+7944G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159251735 | ||||||
| chr4:159251756
|
GTCTGTAA others(17): Show |
G | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.543+7988_543+8011d others(26): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159251756 | |||||
| chr4:159251773
|
A | G | 1 | a0001c0001t0025g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.543+7982A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159251773 | ||||||
| chr4:159251799
|
C | T | 1 | a0001c0001t0002g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.543+8008C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159251799 | ||||||
| chr4:159251853
|
G | A | 41 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(38): Show | 41 | HG00099.hp1 HG00438.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.543+8062G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159251853 | ||||||
| chr4:159251889
|
G | A | 129 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.543+8098G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159251889 | ||||||
| chr4:159251951
|
G | A | 75 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.543+8160G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159251951 | ||||||
| chr4:159252145
|
C | T | 6 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0001t0008g0112others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+8354C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159252145 | ||||||
| chr4:159252193
|
T | G | 3 | a0001c0002t0018g0148a0001c0003t0017g0117a0001c0003t0019g0135 | 3 | HG00735.hp1 HG01081.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.543+8402T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159252193 | ||||||
| chr4:159252509
|
G | A | 12 | a0001c0002t0018g0148a0001c0003t0004g0009a0001c0003t0004g0045others(9): Show | 12 | HG00735.hp1 HG01081.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.543+8718G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159252509 | ||||||
| chr4:159252558
|
C | T | 1 | a0001c0001t0009g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.543+8767C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159252558 | ||||||
| chr4:159252747
|
G | C | 1 | a0001c0002t0001g0108 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.543+8956G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159252747 | ||||||
| chr4:159252759
|
T | C | 75 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.543+8968T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159252759 | ||||||
| chr4:159252790
|
C | T | 40 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(37): Show | 40 | HG00099.hp1 HG00438.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.543+8999C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159252790 | ||||||
| chr4:159252857
|
T | C | 75 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.543+9066T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159252857 | ||||||
| chr4:159253001
|
T | G | 1 | a0001c0001t0002g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.543+9210T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159253001 | ||||||
| chr4:159253058
|
A | G | 6 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0001t0008g0112others(3): Show | 6 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+9267A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159253058 | ||||||
| chr4:159253212
|
A | G | 1 | a0001c0001t0002g0001 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.543+9421A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159253212 | ||||||
| chr4:159253267
|
A | G | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.543+9476A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159253267 | ||||||
| chr4:159253398
|
A | G | 1 | a0001c0002t0001g0054 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.543+9607A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159253398 | ||||||
| chr4:159253561
|
C | T | 75 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.543+9770C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159253561 | ||||||
| chr4:159253575
|
A | G | 1 | a0001c0002t0003g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.543+9784A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159253575 | ||||||
| chr4:159253675
|
A | G | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543+9884A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159253675 | ||||||
| chr4:159253679
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.543+9888T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159253679 | ||||||
| chr4:159253842
|
C | G | 7 | a0001c0001t0009g0035a0001c0001t0010g0155a0001c0001t0010g0162others(4): Show | 7 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+10051C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159253842 | ||||||
| chr4:159253860
|
C | T | 11 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0008g0070others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.543+10069C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159253860 | ||||||
| chr4:159253861
|
G | A | 1 | a0001c0002t0001g0143 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.543+10070G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159253861 | ||||||
| chr4:159253892
|
C | T | 7 | a0001c0001t0009g0035a0001c0001t0010g0155a0001c0001t0010g0162others(4): Show | 7 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+10101C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159253892 | ||||||
| chr4:159253992
|
C | T | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543+10201C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159253992 | ||||||
| chr4:159254049
|
G | A | 12 | a0001c0002t0018g0148a0001c0003t0004g0009a0001c0003t0004g0045others(9): Show | 12 | HG00735.hp1 HG01081.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.543+10258G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159254049 | ||||||
| chr4:159254096
|
C | T | 1 | a0001c0001t0029g0002 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.543+10305C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159254096 | ||||||
| chr4:159254470
|
T | C | 1 | a0001c0001t0002g0132 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.543+10679T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159254470 | ||||||
| chr4:159254503
|
A | G | 16 | a0001c0001t0005g0024a0001c0001t0007g0077a0001c0001t0007g0078others(13): Show | 16 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.543+10712A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159254503 | ||||||
| chr4:159254600
|
C | CT | 22 | a0001c0001t0002g0076a0001c0001t0005g0024a0001c0001t0005g0092others(19): Show | 22 | HG01123.hp1 HG01891.hp2 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.543+10831dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159254600 | |||||
| chr4:159254600
|
C | CTT | 45 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(42): Show | 45 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.543+10830_543+1083 others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159254600 | |||||
| chr4:159254623
|
A | T | 1 | a0001c0001t0010g0165 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.543+10832A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159254623 | ||||||
| chr4:159254736
|
G | A | 7 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0001t0008g0112others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+10945G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159254736 | ||||||
| chr4:159254767
|
C | T | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.543+10976C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159254767 | ||||||
| chr4:159254774
|
A | T | 1 | a0001c0002t0001g0153 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.543+10983A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159254774 | ||||||
| chr4:159254835
|
A | G | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.543+11044A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159254835 | ||||||
| chr4:159255034
|
A | G | 1 | a0001c0001t0002g0098 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.543+11243A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159255034 | ||||||
| chr4:159255275
|
T | A | 1 | a0001c0001t0031g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.543+11484T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159255275 | ||||||
| chr4:159255307
|
C | T | 1 | a0001c0001t0002g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.543+11516C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159255307 | ||||||
| chr4:159255311
|
A | G | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+11520A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159255311 | ||||||
| chr4:159255323
|
C | G | 9 | a0001c0003t0004g0009a0001c0003t0004g0045a0001c0003t0004g0047others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+11532C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159255323 | ||||||
| chr4:159255328
|
C | G | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+11537C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159255328 | ||||||
| chr4:159255356
|
G | GT | 39 | a0001c0001t0002g0025a0001c0001t0002g0076a0001c0001t0002g0079others(36): Show | 39 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.543+11578dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159255356 | |||||
| chr4:159255369
|
T | A | 7 | a0001c0001t0008g0062a0001c0001t0008g0067a0001c0001t0008g0112others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+11578T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159255369 | ||||||
| chr4:159255441
|
T | C | 9 | a0001c0001t0005g0024a0001c0001t0007g0077a0001c0001t0007g0078others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+11650T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159255441 | ||||||
| chr4:159255470
|
C | T | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543+11679C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159255470 | ||||||
| chr4:159255497
|
A | G | 1 | a0001c0001t0007g0082 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.543+11706A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159255497 | ||||||
| chr4:159255766
|
G | A | 38 | a0001c0001t0002g0044a0001c0001t0008g0033a0001c0001t0008g0041others(35): Show | 38 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.543+11975G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159255766 | ||||||
| chr4:159255837
|
A | T | 1 | a0001c0001t0007g0078 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.543+12046A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159255837 | ||||||
| chr4:159255859
|
C | T | 1 | a0001c0002t0001g0111 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.543+12068C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159255859 | ||||||
| chr4:159255880
|
TTATGTCT others(9): Show |
T | 75 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(72): Show | 75 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.543+12093_543+1210 others(20): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159255880 | |||||
| chr4:159256365
|
A | G | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543+12574A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159256365 | ||||||
| chr4:159256425
|
A | C | 130 | a0001c0001t0002g0010a0001c0001t0002g0025a0001c0001t0002g0044others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.543+12634A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159256425 | ||||||
| chr4:159256625
|
T | C | 1 | a0001c0001t0010g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.543+12834T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159256625 | ||||||
| chr4:159256821
|
T | A | 11 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0008g0070others(8): Show | 11 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.543+13030T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159256821 | ||||||
| chr4:159257093
|
TTTTTG | T | 8 | a0001c0001t0005g0024a0001c0001t0008g0062a0001c0001t0008g0067others(5): Show | 8 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.543+13322_543+1332 others(9): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159257093 | |||||
| chr4:159257323
|
A | G | 73 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(70): Show | 73 | HG00099.hp1 HG00438.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.543+13532A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159257323 | ||||||
| chr4:159257607
|
A | G | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543+13816A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159257607 | ||||||
| chr4:159257854
|
C | T | 1 | a0001c0002t0003g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.543+14063C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159257854 | ||||||
| chr4:159257928
|
G | A | 1 | a0001c0002t0001g0042 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.543+14137G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159257928 | ||||||
| chr4:159257961
|
G | A | 54 | a0001c0001t0002g0010a0001c0001t0002g0044a0001c0001t0002g0071others(51): Show | 54 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.543+14170G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159257961 | ||||||
| chr4:159258597
|
G | A | 1 | a0001c0001t0028g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.543+14806G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159258597 | ||||||
| chr4:159258700
|
CTT | C | 2 | a0001c0002t0001g0006a0001c0002t0001g0152 | 2 | HG03239.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.543+14911_543+1491 others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159258700 | |||||
| chr4:159258708
|
C | T | 4 | a0001c0001t0002g0071a0001c0001t0011g0021a0001c0001t0011g0022others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+14917C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159258708 | ||||||
| chr4:159258803
|
C | A | 1 | a0001c0002t0001g0052 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.543+15012C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159258803 | ||||||
| chr4:159259116
|
T | A | 1 | a0001c0001t0002g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.543+15325T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159259116 | ||||||
| chr4:159259332
|
A | G | 1 | a0001c0003t0004g0019 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.543+15541A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159259332 | ||||||
| chr4:159259417
|
C | T | 1 | a0001c0002t0022g0106 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.543+15626C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159259417 | ||||||
| chr4:159259641
|
C | G | 42 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0001t0002g0079others(39): Show | 42 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.543+15850C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159259641 | ||||||
| chr4:159259898
|
A | G | 1 | a0001c0001t0005g0049 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.543+16107A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159259898 | ||||||
| chr4:159259911
|
T | G | 1 | a0001c0001t0002g0079 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.543+16120T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159259911 | ||||||
| chr4:159260045
|
T | C | 3 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085 | 3 | HG02559.hp2 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.543+16254T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159260045 | ||||||
| chr4:159260096
|
C | G | 12 | a0001c0002t0018g0148a0001c0003t0004g0009a0001c0003t0004g0045others(9): Show | 12 | HG00735.hp1 HG01081.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.543+16305C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159260096 | ||||||
| chr4:159260144
|
C | T | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.543+16353C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159260144 | ||||||
| chr4:159260145
|
G | A | 7 | a0001c0001t0002g0154a0001c0001t0008g0062a0001c0001t0008g0067others(4): Show | 7 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.543+16354G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159260145 | ||||||
| chr4:159260222
|
T | C | 132 | a0001c0001t0002g0025a0001c0001t0002g0029a0001c0001t0002g0044others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.543+16431T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159260222 | ||||||
| chr4:159260282
|
AT | A | 5 | a0001c0001t0002g0044a0001c0001t0033g0113a0001c0002t0001g0133others(2): Show | 5 | HG01069.hp1 HG01517.hp1 HG01884.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+16506delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159260282 | |||||
| chr4:159260437
|
T | G | 1 | a0001c0001t0031g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.543+16646T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159260437 | ||||||
| chr4:159260677
|
G | A | 2 | a0001c0002t0001g0133a0001c0002t0001g0134 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.543+16886G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159260677 | ||||||
| chr4:159260793
|
G | A | 1 | a0001c0001t0010g0162 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.543+17002G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159260793 | ||||||
| chr4:159261012
|
C | G | 1 | a0001c0002t0001g0007 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.543+17221C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159261012 | ||||||
| chr4:159261060
|
A | G | 3 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0021g0028 | 3 | HG02970.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.543+17269A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159261060 | ||||||
| chr4:159261067
|
A | AT | 53 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.543+17290dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159261067 | |||||
| chr4:159261101
|
C | T | 6 | a0001c0001t0005g0024a0001c0001t0010g0155a0001c0001t0010g0162others(3): Show | 6 | HG01884.hp2 HG02615.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+17310C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159261101 | ||||||
| chr4:159261162
|
C | T | 1 | a0001c0002t0001g0100 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.543+17371C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159261162 | ||||||
| chr4:159261246
|
T | C | 2 | a0001c0001t0002g0125a0001c0001t0006g0177 | 2 | HG00558.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.543+17455T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159261246 | ||||||
| chr4:159261252
|
T | C | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543+17461T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159261252 | ||||||
| chr4:159261263
|
T | C | 74 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(71): Show | 74 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.543+17472T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159261263 | ||||||
| chr4:159261303
|
T | C | 10 | a0001c0001t0028g0167a0001c0002t0001g0100a0001c0003t0004g0009others(7): Show | 10 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.543+17512T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159261303 | ||||||
| chr4:159261338
|
G | A | 192 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.543+17547G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159261338 | ||||||
| chr4:159261342
|
G | A | 58 | a0001c0001t0002g0005a0001c0001t0002g0076a0001c0001t0002g0099others(55): Show | 58 | HG00597.hp1 HG00735.hp1 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.543+17551G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159261342 | ||||||
| chr4:159261352
|
G | A | 1 | a0001c0001t0010g0165 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.543+17561G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159261352 | ||||||
| chr4:159261723
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.543+17932C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159261723 | ||||||
| chr4:159261868
|
T | G | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+18077T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159261868 | ||||||
| chr4:159261943
|
T | G | 1 | a0001c0002t0001g0139 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.543+18152T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159261943 | ||||||
| chr4:159262135
|
G | T | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.543+18344G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159262135 | ||||||
| chr4:159262164
|
A | G | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.543+18373A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159262164 | ||||||
| chr4:159262378
|
G | C | 128 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(125): Show | 128 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.543+18587G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159262378 | ||||||
| chr4:159262610
|
G | T | 5 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0164others(2): Show | 5 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+18819G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159262610 | ||||||
| chr4:159262699
|
A | G | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543+18908A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159262699 | ||||||
| chr4:159262748
|
G | A | 1 | a0001c0003t0004g0063 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.543+18957G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159262748 | ||||||
| chr4:159262818
|
G | T | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543+19027G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159262818 | ||||||
| chr4:159262826
|
CT | C | 77 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(74): Show | 77 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.543+19046delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159262826 | |||||
| chr4:159263374
|
A | G | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.543+19583A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159263374 | ||||||
| chr4:159263399
|
G | C | 3 | a0001c0003t0004g0019a0001c0003t0017g0117a0001c0003t0019g0135 | 3 | HG01081.hp2 HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.543+19608G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159263399 | ||||||
| chr4:159263466
|
T | A | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.543+19675T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159263466 | ||||||
| chr4:159263506
|
G | T | 76 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(73): Show | 76 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.543+19715G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159263506 | ||||||
| chr4:159263646
|
A | T | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.543+19855A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159263646 | ||||||
| chr4:159263708
|
G | A | 1 | a0001c0001t0006g0163 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.543+19917G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159263708 | ||||||
| chr4:159263991
|
A | G | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.543+20200A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159263991 | ||||||
| chr4:159264030
|
G | A | 3 | a0001c0001t0002g0090a0001c0001t0002g0122a0001c0001t0002g0144 | 3 | HG02257.hp2 HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.543+20239G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159264030 | ||||||
| chr4:159264517
|
C | T | 45 | a0001c0001t0002g0060a0001c0001t0008g0033a0001c0001t0008g0041others(42): Show | 45 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.543+20726C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159264517 | ||||||
| chr4:159264585
|
A | G | 1 | a0001c0002t0001g0108 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.543+20794A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159264585 | ||||||
| chr4:159264592
|
A | G | 1 | a0001c0001t0009g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.543+20801A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159264592 | ||||||
| chr4:159264597
|
C | A | 1 | a0001c0001t0009g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.543+20806C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159264597 | ||||||
| chr4:159264679
|
A | C | 1 | a0001c0001t0009g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.543+20888A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159264679 | ||||||
| chr4:159264802
|
G | A | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.543+21011G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159264802 | ||||||
| chr4:159264945
|
G | A | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543+21154G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159264945 | ||||||
| chr4:159264967
|
A | G | 20 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0005g0092others(17): Show | 20 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.543+21176A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159264967 | ||||||
| chr4:159265042
|
T | C | 9 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0005g0092others(6): Show | 9 | HG02818.hp2 HG02922.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+21251T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159265042 | ||||||
| chr4:159265132
|
T | C | 70 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.543+21341T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159265132 | ||||||
| chr4:159265169
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.543+21378C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159265169 | ||||||
| chr4:159265334
|
G | C | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.543+21543G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159265334 | ||||||
| chr4:159265466
|
C | G | 4 | a0001c0001t0002g0071a0001c0001t0011g0021a0001c0001t0011g0022others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+21675C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159265466 | ||||||
| chr4:159265520
|
G | A | 21 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0005g0092others(18): Show | 21 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.543+21729G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159265520 | ||||||
| chr4:159265966
|
C | G | 70 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.543+22175C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159265966 | ||||||
| chr4:159266101
|
T | C | 3 | a0001c0001t0002g0149a0001c0001t0008g0067a0001c0001t0008g0112 | 3 | HG00558.hp2 HG01943.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.543+22310T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159266101 | ||||||
| chr4:159266344
|
A | G | 70 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.543+22553A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159266344 | ||||||
| chr4:159266365
|
T | C | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.543+22574T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159266365 | ||||||
| chr4:159266578
|
T | A | 2 | a0001c0001t0002g0066a0001c0002t0003g0168 | 2 | HG01981.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.543+22787T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159266578 | ||||||
| chr4:159266579
|
A | T | 45 | a0001c0001t0002g0060a0001c0001t0008g0033a0001c0001t0008g0041others(42): Show | 45 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.543+22788A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159266579 | ||||||
| chr4:159266676
|
C | G | 1 | a0001c0002t0001g0046 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.543+22885C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159266676 | ||||||
| chr4:159267791
|
C | CT | 17 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(14): Show | 17 | HG01081.hp2 HG01123.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.543+24016dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159267791 | |||||
| chr4:159268041
|
C | T | 1 | a0001c0001t0008g0067 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.543+24250C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159268041 | ||||||
| chr4:159268048
|
C | CT | 70 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.543+24268dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159268048 | |||||
| chr4:159268048
|
CT | C | 6 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0164others(3): Show | 6 | HG01884.hp2 HG02257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+24268delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159268048 | |||||
| chr4:159268351
|
G | C | 3 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085 | 3 | HG02559.hp2 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.543+24560G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159268351 | ||||||
| chr4:159268435
|
C | T | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543+24644C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159268435 | ||||||
| chr4:159268585
|
G | A | 2 | a0001c0002t0003g0188a0001c0002t0003g0192 | 2 | HG01978.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.543+24794G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159268585 | ||||||
| chr4:159268963
|
C | A | 45 | a0001c0001t0002g0060a0001c0001t0008g0033a0001c0001t0008g0041others(42): Show | 45 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.543+25172C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159268963 | ||||||
| chr4:159268982
|
A | G | 2 | a0001c0002t0012g0151a0001c0002t0012g0156 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.543+25191A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159268982 | ||||||
| chr4:159269010
|
G | A | 129 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.543+25219G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159269010 | ||||||
| chr4:159269028
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.543+25237A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159269028 | ||||||
| chr4:159269087
|
C | A | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543+25296C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159269087 | ||||||
| chr4:159269455
|
T | C | 1 | a0001c0001t0021g0028 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.543+25664T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159269455 | ||||||
| chr4:159269676
|
T | G | 1 | a0001c0001t0002g0010 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.543+25885T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159269676 | ||||||
| chr4:159269691
|
G | A | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543+25900G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159269691 | ||||||
| chr4:159269913
|
T | C | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.543+26122T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159269913 | ||||||
| chr4:159270018
|
A | G | 3 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085 | 3 | HG02559.hp2 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.543+26227A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159270018 | ||||||
| chr4:159270365
|
C | T | 1 | a0001c0002t0001g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.543+26574C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159270365 | ||||||
| chr4:159270423
|
T | A | 3 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0003g0186 | 3 | HG01516.hp2 HG01517.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.543+26632T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159270423 | ||||||
| chr4:159270570
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.543+26779A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159270570 | ||||||
| chr4:159270686
|
A | G | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543+26895A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159270686 | ||||||
| chr4:159270908
|
C | T | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.543+27117C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159270908 | ||||||
| chr4:159271181
|
A | G | 5 | a0001c0001t0008g0070a0001c0001t0029g0002a0001c0001t0033g0113others(2): Show | 5 | HG02922.hp1 HG02976.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+27390A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159271181 | ||||||
| chr4:159271332
|
T | A | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.543+27541T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159271332 | ||||||
| chr4:159271970
|
C | G | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.543+28179C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159271970 | ||||||
| chr4:159272063
|
T | A | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.543+28272T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159272063 | ||||||
| chr4:159272074
|
A | G | 5 | a0001c0001t0002g0025a0001c0001t0005g0049a0001c0002t0001g0004others(2): Show | 5 | NA18955.hp1 NA18961.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+28283A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159272074 | ||||||
| chr4:159272088
|
A | G | 51 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.543+28297A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159272088 | ||||||
| chr4:159272089
|
G | C | 9 | a0001c0001t0004g0193a0001c0001t0024g0087a0001c0002t0001g0157others(6): Show | 9 | HG02630.hp1 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.543+28298G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159272089 | ||||||
| chr4:159272151
|
G | A | 2 | a0001c0001t0008g0070a0001c0005t0005g0016 | 2 | HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.543+28360G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159272151 | ||||||
| chr4:159272503
|
C | G | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.543+28712C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159272503 | ||||||
| chr4:159272595
|
G | A | 3 | a0001c0002t0001g0040a0001c0002t0001g0054a0001c0002t0001g0055 | 3 | HG00733.hp1 HG01109.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.543+28804G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159272595 | ||||||
| chr4:159272759
|
A | C | 1 | a0001c0001t0002g0149 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.543+28968A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159272759 | ||||||
| chr4:159272992
|
G | T | 10 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0005g0092others(7): Show | 10 | HG02622.hp2 HG02818.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.543+29201G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159272992 | ||||||
| chr4:159273161
|
A | C | 9 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0005g0092others(6): Show | 9 | HG02818.hp2 HG02922.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+29370A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159273161 | ||||||
| chr4:159273212
|
G | A | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.543+29421G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159273212 | ||||||
| chr4:159273364
|
A | G | 1 | a0001c0001t0002g0109 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.543+29573A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159273364 | ||||||
| chr4:159273377
|
A | G | 10 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0005g0092others(7): Show | 10 | HG02622.hp2 HG02818.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.543+29586A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159273377 | ||||||
| chr4:159273490
|
CT | C | 26 | a0001c0001t0002g0044a0001c0001t0002g0099a0001c0001t0004g0193others(23): Show | 26 | HG00099.hp1 HG00735.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.543+29700delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159273490 | ||||||
| chr4:159273611
|
T | G | 5 | a0001c0001t0002g0149a0001c0001t0005g0024a0001c0001t0008g0062others(2): Show | 5 | HG00558.hp2 HG01943.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.543+29820T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159273611 | ||||||
| chr4:159273626
|
G | GTTTC | 5 | a0001c0001t0002g0103a0001c0001t0005g0012a0001c0001t0011g0022others(2): Show | 5 | HG01978.hp2 HG01993.hp1 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+29909_543+2991 others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159273626 | |||||
| chr4:159273626
|
G | GTTTCTTT others(1): Show |
2 | a0001c0001t0009g0035a0001c0001t0010g0164 | 2 | HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.543+29905_543+2991 others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159273626 | |||||
| chr4:159273626
|
GTTTC | G | 44 | a0001c0001t0002g0044a0001c0001t0002g0071a0001c0001t0002g0088others(41): Show | 44 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.543+29909_543+2991 others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159273626 | |||||
| chr4:159273626
|
GTTTCTTT others(1): Show |
G | 52 | a0001c0001t0002g0060a0001c0001t0002g0079a0001c0001t0002g0089others(49): Show | 52 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.543+29905_543+2991 others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159273626 | |||||
| chr4:159273626
|
GTTTCTTT others(5): Show |
G | 34 | a0001c0001t0002g0001a0001c0001t0002g0029a0001c0001t0002g0074others(31): Show | 34 | HG00642.hp1 HG00733.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.543+29901_543+2991 others(16): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159273626 | |||||
| chr4:159273626
|
GTTTCTTT others(9): Show |
G | 16 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0025others(13): Show | 16 | HG00597.hp1 HG01261.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.543+29897_543+2991 others(20): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159273626 | |||||
| chr4:159273626
|
GTTTCTTT others(13): Show |
G | 2 | a0001c0001t0002g0076a0001c0001t0004g0194 | 2 | HG02486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.543+29893_543+2991 others(24): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159273626 | |||||
| chr4:159273626
|
GTTTCTTT others(17): Show |
G | 3 | a0001c0001t0002g0066a0001c0001t0005g0049a0001c0001t0007g0077 | 3 | HG03098.hp2 HG04228.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.543+29889_543+2991 others(28): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159273626 | |||||
| chr4:159273626
|
GTTTCTTT others(21): Show |
G | 1 | a0001c0002t0001g0048 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.543+29885_543+2991 others(32): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159273626 | |||||
| chr4:159273628
|
TTCTTTCT others(3): Show |
T | 1 | a0001c0001t0008g0112 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.543+29839_543+2984 others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159273628 | |||||
| chr4:159273639
|
T | C | 1 | a0001c0001t0031g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.543+29848T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159273639 | ||||||
| chr4:159273686
|
CTTTCTTT others(6): Show |
C | 1 | a0001c0001t0006g0187 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.543+29898_543+2991 others(17): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159273686 | |||||
| chr4:159273823
|
C | T | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.543+30032C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159273823 | ||||||
| chr4:159273853
|
C | T | 1 | a0001c0001t0002g0001 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.543+30062C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159273853 | ||||||
| chr4:159273912
|
C | T | 1 | a0001c0002t0003g0168 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.543+30121C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159273912 | ||||||
| chr4:159273950
|
C | T | 1 | a0001c0002t0001g0100 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.543+30159C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159273950 | ||||||
| chr4:159274014
|
G | A | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.543+30223G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159274014 | ||||||
| chr4:159274428
|
A | T | 1 | a0001c0002t0001g0158 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.544-29914A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159274428 | ||||||
| chr4:159274533
|
A | G | 1 | a0001c0001t0006g0170 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.544-29809A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159274533 | ||||||
| chr4:159274624
|
C | G | 129 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(126): Show | 129 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.544-29718C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159274624 | ||||||
| chr4:159275001
|
T | C | 1 | a0001c0001t0006g0183 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.544-29341T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159275001 | ||||||
| chr4:159275029
|
T | A | 1 | a0001c0001t0028g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.544-29313T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159275029 | ||||||
| chr4:159275054
|
C | CGT | 19 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0076others(16): Show | 19 | HG00597.hp2 HG00733.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.544-29247_544-2924 others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159275054 | |||||
| chr4:159275054
|
C | CGTGT | 16 | a0001c0001t0002g0010a0001c0001t0002g0057a0001c0001t0002g0071others(13): Show | 16 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(13): Show |
intron_variant | MODIFIER | c.544-29249_544-2924 others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159275054 | |||||
| chr4:159275054
|
C | CGTGTGT | 6 | a0001c0001t0002g0091a0001c0001t0002g0097a0001c0001t0002g0131others(3): Show | 6 | HG01074.hp1 HG01167.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-29251_544-2924 others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159275054 | |||||
| chr4:159275054
|
CGT | C | 39 | a0001c0001t0002g0066a0001c0001t0002g0090a0001c0001t0005g0012others(36): Show | 39 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.544-29247_544-2924 others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159275054 | |||||
| chr4:159275054
|
CGTGT | C | 42 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0099others(39): Show | 42 | HG00099.hp1 HG00280.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.544-29249_544-2924 others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159275054 | |||||
| chr4:159275054
|
CGTGTGT | C | 14 | a0001c0001t0002g0060a0001c0001t0002g0079a0001c0001t0004g0193others(11): Show | 14 | HG00438.hp2 HG00738.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.544-29251_544-2924 others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159275054 | |||||
| chr4:159275054
|
CGTGTGTG others(1): Show |
C | 13 | a0001c0001t0005g0049a0001c0001t0007g0077a0001c0001t0007g0078others(10): Show | 13 | HG01891.hp2 HG01981.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.544-29253_544-2924 others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159275054 | |||||
| chr4:159275054
|
CGTGTGTG others(3): Show |
C | 2 | a0001c0001t0002g0074a0001c0011t0032g0114 | 2 | HG02257.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.544-29255_544-2924 others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159275054 | |||||
| chr4:159275054
|
CGTGTGTG others(5): Show |
C | 2 | a0001c0001t0009g0058a0001c0002t0003g0168 | 2 | HG01981.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.544-29257_544-2924 others(16): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159275054 | |||||
| chr4:159275054
|
CGTGTGTG others(7): Show |
C | 2 | a0001c0001t0006g0161a0001c0005t0005g0016 | 2 | HG02040.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.544-29259_544-2924 others(18): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159275054 | |||||
| chr4:159275054
|
CGTGTGTG others(9): Show |
C | 2 | a0001c0001t0009g0059a0001c0002t0003g0169 | 2 | HG03540.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.544-29261_544-2924 others(20): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159275054 | |||||
| chr4:159275104
|
A | G | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-29238A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159275104 | ||||||
| chr4:159275452
|
A | G | 1 | a0001c0002t0001g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.544-28890A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159275452 | ||||||
| chr4:159275481
|
C | T | 129 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.544-28861C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159275481 | ||||||
| chr4:159275516
|
A | G | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-28826A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159275516 | ||||||
| chr4:159275952
|
T | C | 4 | a0001c0001t0002g0149a0001c0001t0008g0062a0001c0001t0008g0067others(1): Show | 4 | HG00558.hp2 HG01943.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-28390T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159275952 | ||||||
| chr4:159276154
|
C | T | 1 | a0001c0001t0021g0028 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.544-28188C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159276154 | ||||||
| chr4:159276259
|
T | A | 2 | a0001c0001t0004g0194a0001c0001t0021g0028 | 2 | HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.544-28083T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159276259 | ||||||
| chr4:159276313
|
A | G | 1 | a0001c0001t0028g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.544-28029A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159276313 | ||||||
| chr4:159276667
|
T | C | 4 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0164others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-27675T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159276667 | ||||||
| chr4:159276846
|
C | CA | 63 | a0001c0001t0002g0060a0001c0001t0002g0149a0001c0001t0005g0024others(60): Show | 63 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.544-27486dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159276846 | |||||
| chr4:159276971
|
C | T | 1 | a0001c0002t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.544-27371C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159276971 | ||||||
| chr4:159276987
|
A | T | 3 | a0001c0001t0009g0058a0001c0001t0009g0059a0001c0002t0003g0168 | 3 | HG01981.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.544-27355A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159276987 | ||||||
| chr4:159277072
|
C | G | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-27270C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159277072 | ||||||
| chr4:159277097
|
A | G | 128 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(125): Show | 128 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.544-27245A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159277097 | ||||||
| chr4:159277170
|
A | G | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-27172A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159277170 | ||||||
| chr4:159277365
|
G | A | 129 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(126): Show | 129 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.544-26977G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159277365 | ||||||
| chr4:159277480
|
G | A | 45 | a0001c0001t0002g0060a0001c0001t0008g0033a0001c0001t0008g0041others(42): Show | 45 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.544-26862G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159277480 | ||||||
| chr4:159277514
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.544-26828A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159277514 | ||||||
| chr4:159277532
|
A | G | 1 | a0001c0001t0028g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.544-26810A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159277532 | ||||||
| chr4:159277700
|
A | G | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.544-26642A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159277700 | ||||||
| chr4:159277713
|
A | G | 3 | a0001c0001t0002g0005a0001c0007t0016g0140a0001c0007t0016g0141 | 3 | HG01884.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.544-26629A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159277713 | ||||||
| chr4:159277934
|
A | G | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.544-26408A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159277934 | ||||||
| chr4:159278019
|
G | T | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.544-26323G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159278019 | ||||||
| chr4:159278106
|
C | T | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.544-26236C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159278106 | ||||||
| chr4:159278107
|
C | G | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.544-26235C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159278107 | ||||||
| chr4:159278114
|
T | A | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.544-26228T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159278114 | ||||||
| chr4:159278161
|
A | G | 1 | a0001c0002t0003g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.544-26181A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159278161 | ||||||
| chr4:159278190
|
G | A | 2 | a0001c0001t0004g0194a0001c0001t0021g0028 | 2 | HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.544-26152G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159278190 | ||||||
| chr4:159278266
|
A | G | 1 | a0001c0003t0004g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.544-26076A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159278266 | ||||||
| chr4:159278267
|
T | G | 1 | a0001c0003t0004g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.544-26075T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159278267 | ||||||
| chr4:159278452
|
C | G | 1 | a0001c0001t0002g0125 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.544-25890C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159278452 | ||||||
| chr4:159278568
|
A | G | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.544-25774A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159278568 | ||||||
| chr4:159278631
|
T | C | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-25711T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159278631 | ||||||
| chr4:159278749
|
G | A | 1 | a0001c0001t0031g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.544-25593G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159278749 | ||||||
| chr4:159279198
|
C | T | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-25144C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159279198 | ||||||
| chr4:159279199
|
A | G | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.544-25143A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159279199 | ||||||
| chr4:159279309
|
C | T | 1 | a0001c0002t0003g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.544-25033C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159279309 | ||||||
| chr4:159279310
|
G | A | 12 | a0001c0003t0004g0009a0001c0003t0004g0019a0001c0003t0004g0045others(9): Show | 12 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.544-25032G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159279310 | ||||||
| chr4:159279526
|
C | G | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-24816C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159279526 | ||||||
| chr4:159279561
|
C | T | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.544-24781C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159279561 | ||||||
| chr4:159279826
|
G | A | 3 | a0001c0002t0001g0027a0001c0002t0001g0038a0001c0002t0001g0039 | 3 | HG01069.hp2 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.544-24516G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159279826 | ||||||
| chr4:159279874
|
G | A | 4 | a0001c0001t0002g0071a0001c0001t0011g0021a0001c0001t0011g0022others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-24468G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159279874 | ||||||
| chr4:159279986
|
A | G | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.544-24356A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159279986 | ||||||
| chr4:159280041
|
T | C | 1 | a0001c0001t0002g0057 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.544-24301T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159280041 | ||||||
| chr4:159280106
|
T | A | 1 | a0001c0002t0001g0158 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.544-24236T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159280106 | ||||||
| chr4:159280128
|
A | G | 1 | a0001c0002t0001g0139 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.544-24214A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159280128 | ||||||
| chr4:159280244
|
C | G | 3 | a0001c0002t0001g0027a0001c0002t0001g0038a0001c0002t0001g0039 | 3 | HG01069.hp2 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.544-24098C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159280244 | ||||||
| chr4:159280572
|
A | G | 49 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.544-23770A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159280572 | ||||||
| chr4:159280638
|
A | G | 1 | a0001c0001t0002g0015 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.544-23704A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159280638 | ||||||
| chr4:159280723
|
T | C | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-23619T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159280723 | ||||||
| chr4:159280799
|
A | C | 1 | a0001c0002t0001g0157 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.544-23543A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159280799 | ||||||
| chr4:159280894
|
A | G | 51 | a0001c0001t0002g0060a0001c0001t0002g0149a0001c0001t0005g0024others(48): Show | 51 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.544-23448A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159280894 | ||||||
| chr4:159280955
|
T | G | 51 | a0001c0001t0002g0060a0001c0001t0002g0149a0001c0001t0005g0024others(48): Show | 51 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.544-23387T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159280955 | ||||||
| chr4:159280982
|
A | ACTT | 104 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(101): Show | 104 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(101): Show |
intron_variant | MODIFIER | c.544-23356_544-2335 others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159280982 | |||||
| chr4:159280986
|
C | CTTCT | 18 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(15): Show | 18 | HG01081.hp2 HG02559.hp2 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.544-23354_544-2335 others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159280986 | |||||
| chr4:159280986
|
C | CTTCTT | 9 | a0001c0003t0004g0009a0001c0003t0004g0045a0001c0003t0004g0047others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.544-23354_544-2335 others(9): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159280986 | |||||
| chr4:159281155
|
C | T | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-23187C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159281155 | ||||||
| chr4:159281392
|
GGCATGGT others(20): Show |
G | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.544-22946_544-2292 others(31): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159281392 | |||||
| chr4:159281473
|
C | T | 1 | a0001c0001t0028g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.544-22869C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159281473 | ||||||
| chr4:159281608
|
T | G | 1 | a0001c0001t0007g0078 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.544-22734T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159281608 | ||||||
| chr4:159281671
|
C | CA | 6 | a0001c0001t0002g0071a0001c0001t0002g0098a0001c0001t0002g0154others(3): Show | 6 | HG01934.hp2 HG02258.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-22652dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159281671 | |||||
| chr4:159281671
|
CA | C | 51 | a0001c0001t0002g0060a0001c0001t0002g0149a0001c0001t0005g0024others(48): Show | 51 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.544-22652delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159281671 | |||||
| chr4:159281687
|
A | AAG | 47 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(44): Show | 47 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.544-22654_544-2265 others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159281687 | |||||
| chr4:159281687
|
A | AG | 28 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(25): Show | 28 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.544-22655_544-2265 others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159281687 | ||||||
| chr4:159281687
|
A | G | 1 | a0001c0002t0003g0169 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.544-22655A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159281687 | ||||||
| chr4:159282034
|
TG | T | 5 | a0001c0001t0002g0149a0001c0001t0005g0024a0001c0001t0008g0062others(2): Show | 5 | HG00558.hp2 HG01943.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-22307delG | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159282034 | ||||||
| chr4:159282481
|
A | G | 1 | a0001c0002t0003g0008 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.544-21861A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159282481 | ||||||
| chr4:159282765
|
G | A | 26 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(23): Show | 26 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.544-21577G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159282765 | ||||||
| chr4:159282765
|
G | T | 1 | a0001c0001t0021g0028 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.544-21577G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159282765 | ||||||
| chr4:159282844
|
C | T | 51 | a0001c0001t0002g0060a0001c0001t0002g0149a0001c0001t0005g0024others(48): Show | 51 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.544-21498C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159282844 | ||||||
| chr4:159282864
|
C | T | 2 | a0001c0004t0001g0020a0001c0004t0003g0159 | 2 | HG00280.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.544-21478C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159282864 | ||||||
| chr4:159283008
|
T | A | 5 | a0001c0001t0002g0149a0001c0001t0005g0024a0001c0001t0008g0062others(2): Show | 5 | HG00558.hp2 HG01943.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-21334T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159283008 | ||||||
| chr4:159283120
|
G | T | 45 | a0001c0001t0002g0060a0001c0001t0008g0033a0001c0001t0008g0041others(42): Show | 45 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.544-21222G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159283120 | ||||||
| chr4:159283125
|
A | G | 43 | a0001c0001t0002g0060a0001c0001t0008g0033a0001c0001t0008g0041others(40): Show | 43 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.544-21217A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159283125 | ||||||
| chr4:159283190
|
A | G | 1 | a0001c0001t0006g0177 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.544-21152A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159283190 | ||||||
| chr4:159283219
|
G | A | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.544-21123G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159283219 | ||||||
| chr4:159283319
|
A | G | 2 | a0001c0001t0005g0092a0001c0001t0005g0093 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.544-21023A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159283319 | ||||||
| chr4:159283327
|
TC | T | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-21013delC | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159283327 | |||||
| chr4:159283350
|
TACATGTC others(1): Show |
T | 3 | a0001c0002t0001g0157a0001c0002t0003g0178a0001c0002t0003g0180 | 3 | HG02717.hp2 HG02723.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.544-20990_544-2098 others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159283350 | |||||
| chr4:159283357
|
C | T | 1 | a0001c0002t0001g0006 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.544-20985C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159283357 | ||||||
| chr4:159283712
|
A | G | 1 | a0001c0001t0031g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.544-20630A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159283712 | ||||||
| chr4:159283769
|
A | T | 2 | a0001c0001t0004g0194a0001c0001t0021g0028 | 2 | HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.544-20573A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159283769 | ||||||
| chr4:159284080
|
A | G | 49 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.544-20262A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159284080 | ||||||
| chr4:159284168
|
C | G | 50 | a0001c0001t0002g0149a0001c0001t0005g0024a0001c0001t0008g0033others(47): Show | 50 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.544-20174C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159284168 | ||||||
| chr4:159284210
|
A | G | 45 | a0001c0001t0002g0060a0001c0001t0008g0033a0001c0001t0008g0041others(42): Show | 45 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.544-20132A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159284210 | ||||||
| chr4:159284213
|
G | T | 4 | a0001c0001t0002g0071a0001c0001t0011g0021a0001c0001t0011g0022others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-20129G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159284213 | ||||||
| chr4:159284481
|
GAC | G | 6 | a0001c0001t0002g0001a0001c0001t0002g0057a0001c0001t0002g0089others(3): Show | 6 | HG00597.hp2 HG02615.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-19808_544-1980 others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159284481 | |||||
| chr4:159284481
|
GACAC | G | 10 | a0001c0001t0002g0066a0001c0001t0002g0101a0001c0001t0002g0131others(7): Show | 10 | HG00438.hp1 HG01109.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.544-19810_544-1980 others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159284481 | |||||
| chr4:159284481
|
GACACAC | G | 24 | a0001c0001t0002g0010a0001c0001t0002g0015a0001c0001t0002g0029others(21): Show | 24 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.544-19812_544-1980 others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159284481 | |||||
| chr4:159284481
|
GACACACA others(1): Show |
G | 20 | a0001c0001t0002g0005a0001c0001t0002g0071a0001c0001t0002g0103others(17): Show | 20 | HG00558.hp1 HG00558.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.544-19814_544-1980 others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159284481 | |||||
| chr4:159284481
|
GACACACA others(3): Show |
G | 11 | a0001c0001t0002g0088a0001c0001t0002g0098a0001c0001t0005g0024others(8): Show | 11 | HG00280.hp1 HG01099.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.544-19816_544-1980 others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159284481 | |||||
| chr4:159284481
|
GACACACA others(5): Show |
G | 8 | a0001c0001t0002g0079a0001c0001t0008g0112a0001c0001t0013g0084others(5): Show | 8 | HG01123.hp2 HG01517.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-19818_544-1980 others(16): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159284481 | |||||
| chr4:159284481
|
GACACACA others(7): Show |
G | 14 | a0001c0001t0008g0033a0001c0001t0008g0041a0001c0001t0026g0003others(11): Show | 14 | HG01433.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.544-19820_544-1980 others(18): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159284481 | |||||
| chr4:159284481
|
GACACACA others(9): Show |
G | 10 | a0001c0001t0009g0058a0001c0001t0009g0059a0001c0002t0001g0042others(7): Show | 10 | HG00738.hp2 HG01081.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-19822_544-1980 others(20): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159284481 | |||||
| chr4:159284481
|
GACACACA others(11): Show |
G | 70 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(67): Show | 70 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.544-19824_544-1980 others(22): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159284481 | |||||
| chr4:159284481
|
GACACACA others(13): Show |
G | 1 | a0001c0001t0020g0120 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.544-19826_544-1980 others(24): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159284481 | |||||
| chr4:159284481
|
GACACACA others(19): Show |
G | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.544-19832_544-1980 others(30): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159284481 | |||||
| chr4:159284481
|
GACACACA others(21): Show |
G | 6 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0005g0092others(3): Show | 6 | HG02818.hp2 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-19834_544-1980 others(32): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159284481 | |||||
| chr4:159284482
|
ACACACAC others(4): Show |
A | 1 | a0001c0002t0001g0034 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.544-19859_544-1984 others(15): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159284482 | ||||||
| chr4:159284508
|
ACACACAC others(21): Show |
A | 1 | a0001c0001t0029g0002 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.544-19833_544-1980 others(32): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159284508 | ||||||
| chr4:159284548
|
A | T | 1 | a0001c0001t0006g0177 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.544-19794A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159284548 | ||||||
| chr4:159284560
|
G | A | 1 | a0001c0001t0020g0120 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.544-19782G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159284560 | ||||||
| chr4:159284575
|
G | A | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-19767G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159284575 | ||||||
| chr4:159284621
|
T | C | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-19721T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159284621 | ||||||
| chr4:159284719
|
A | G | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-19623A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159284719 | ||||||
| chr4:159284751
|
T | C | 1 | a0001c0002t0001g0108 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.544-19591T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159284751 | ||||||
| chr4:159284801
|
G | C | 129 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.544-19541G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159284801 | ||||||
| chr4:159285056
|
G | A | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.544-19286G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159285056 | ||||||
| chr4:159285081
|
G | A | 2 | a0001c0001t0008g0033a0001c0001t0008g0041 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.544-19261G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159285081 | ||||||
| chr4:159285100
|
A | G | 43 | a0001c0001t0002g0060a0001c0001t0008g0033a0001c0001t0008g0041others(40): Show | 43 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.544-19242A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159285100 | ||||||
| chr4:159285263
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.544-19079G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159285263 | ||||||
| chr4:159285424
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.544-18918A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159285424 | ||||||
| chr4:159285465
|
A | G | 41 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.544-18877A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159285465 | ||||||
| chr4:159285586
|
T | C | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-18756T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159285586 | ||||||
| chr4:159285592
|
C | T | 1 | a0001c0002t0001g0158 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.544-18750C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159285592 | ||||||
| chr4:159285720
|
A | T | 1 | a0001c0002t0001g0139 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.544-18622A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159285720 | ||||||
| chr4:159285770
|
C | T | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-18572C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159285770 | ||||||
| chr4:159285790
|
C | G | 1 | a0001c0001t0006g0187 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.544-18552C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159285790 | ||||||
| chr4:159285833
|
G | A | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.544-18509G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159285833 | ||||||
| chr4:159286025
|
C | T | 4 | a0001c0001t0002g0149a0001c0001t0008g0062a0001c0001t0008g0067others(1): Show | 4 | HG00558.hp2 HG01943.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-18317C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159286025 | ||||||
| chr4:159286030
|
A | AACC | 39 | a0001c0001t0002g0015a0001c0001t0002g0074a0001c0001t0002g0076others(36): Show | 39 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.544-18262_544-1826 others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159286030 | |||||
| chr4:159286030
|
A | AACCACC | 26 | a0001c0001t0002g0029a0001c0001t0002g0057a0001c0001t0002g0079others(23): Show | 26 | HG00099.hp1 HG00280.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.544-18265_544-1826 others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159286030 | |||||
| chr4:159286030
|
A | AACCACCA others(2): Show |
14 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0071others(11): Show | 14 | HG00438.hp1 HG00558.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.544-18268_544-1826 others(13): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159286030 | |||||
| chr4:159286030
|
A | AACCACCA others(5): Show |
7 | a0001c0001t0002g0044a0001c0001t0002g0066a0001c0001t0002g0132others(4): Show | 7 | HG00639.hp1 HG01069.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-18271_544-1826 others(16): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159286030 | |||||
| chr4:159286030
|
AACC | A | 10 | a0001c0001t0006g0175a0001c0001t0010g0155a0001c0001t0010g0162others(7): Show | 10 | HG00280.hp2 HG01071.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.544-18262_544-1826 others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159286030 | |||||
| chr4:159286030
|
AACCACCA others(2): Show |
A | 10 | a0001c0001t0002g0096a0001c0001t0002g0149a0001c0001t0005g0024others(7): Show | 10 | HG00558.hp2 HG00735.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.544-18268_544-1826 others(13): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159286030 | |||||
| chr4:159286030
|
AACCACCA others(5): Show |
A | 2 | a0001c0001t0026g0003a0001c0001t0029g0002 | 2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.544-18271_544-1826 others(16): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159286030 | |||||
| chr4:159286030
|
AACCACCA others(8): Show |
A | 12 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0005g0092others(9): Show | 12 | HG01081.hp2 HG02818.hp2 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.544-18274_544-1826 others(19): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159286030 | |||||
| chr4:159286030
|
AACCACCA others(11): Show |
A | 11 | a0001c0001t0008g0033a0001c0001t0008g0041a0001c0001t0028g0167others(8): Show | 11 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.544-18277_544-1826 others(22): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159286030 | |||||
| chr4:159286227
|
C | T | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.544-18115C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159286227 | ||||||
| chr4:159286390
|
G | A | 1 | a0001c0002t0001g0107 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.544-17952G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159286390 | ||||||
| chr4:159286403
|
A | C | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.544-17939A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159286403 | ||||||
| chr4:159286403
|
A | T | 76 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(73): Show | 76 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.544-17939A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159286403 | ||||||
| chr4:159286433
|
C | G | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-17909C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159286433 | ||||||
| chr4:159286634
|
C | T | 1 | a0001c0001t0002g0057 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.544-17708C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159286634 | ||||||
| chr4:159287081
|
G | C | 1 | a0001c0002t0001g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.544-17261G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159287081 | ||||||
| chr4:159287410
|
C | T | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-16932C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159287410 | ||||||
| chr4:159287413
|
T | C | 41 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.544-16929T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159287413 | ||||||
| chr4:159287456
|
AC | A | 3 | a0001c0003t0004g0019a0001c0003t0017g0117a0001c0003t0019g0135 | 3 | HG01081.hp2 HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.544-16885delC | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159287456 | ||||||
| chr4:159287478
|
G | A | 130 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.544-16864G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159287478 | ||||||
| chr4:159287499
|
C | T | 1 | a0001c0002t0003g0173 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.544-16843C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159287499 | ||||||
| chr4:159287522
|
T | C | 1 | a0001c0001t0002g0015 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.544-16820T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159287522 | ||||||
| chr4:159287532
|
G | A | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-16810G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159287532 | ||||||
| chr4:159287809
|
A | G | 49 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.544-16533A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159287809 | ||||||
| chr4:159287848
|
T | C | 4 | a0001c0002t0001g0075a0001c0002t0001g0153a0001c0002t0001g0158others(1): Show | 4 | HG00597.hp1 HG01516.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-16494T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159287848 | ||||||
| chr4:159287996
|
C | A | 1 | a0001c0002t0003g0169 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.544-16346C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159287996 | ||||||
| chr4:159288308
|
A | G | 9 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0005g0092others(6): Show | 9 | HG02818.hp2 HG02922.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.544-16034A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159288308 | ||||||
| chr4:159288321
|
G | A | 1 | a0001c0001t0002g0121 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.544-16021G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159288321 | ||||||
| chr4:159288367
|
C | A | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.544-15975C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159288367 | ||||||
| chr4:159288470
|
A | G | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-15872A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159288470 | ||||||
| chr4:159288503
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.544-15839C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159288503 | ||||||
| chr4:159288651
|
A | G | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-15691A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159288651 | ||||||
| chr4:159288664
|
G | A | 76 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(73): Show | 76 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.544-15678G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159288664 | ||||||
| chr4:159289010
|
C | T | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.544-15332C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159289010 | ||||||
| chr4:159289210
|
C | A | 49 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(46): Show | 49 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.544-15132C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159289210 | ||||||
| chr4:159289465
|
G | A | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-14877G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159289465 | ||||||
| chr4:159289692
|
A | G | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-14650A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159289692 | ||||||
| chr4:159289710
|
A | G | 51 | a0001c0001t0002g0060a0001c0001t0002g0149a0001c0001t0005g0024others(48): Show | 51 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.544-14632A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159289710 | ||||||
| chr4:159289808
|
G | A | 1 | a0001c0001t0031g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.544-14534G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159289808 | ||||||
| chr4:159289898
|
A | G | 5 | a0001c0001t0002g0149a0001c0001t0005g0024a0001c0001t0008g0062others(2): Show | 5 | HG00558.hp2 HG01943.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-14444A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159289898 | ||||||
| chr4:159289998
|
C | A | 1 | a0001c0002t0001g0054 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.544-14344C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159289998 | ||||||
| chr4:159290034
|
A | G | 1 | a0001c0001t0009g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.544-14308A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159290034 | ||||||
| chr4:159290080
|
A | G | 51 | a0001c0001t0002g0060a0001c0001t0002g0149a0001c0001t0005g0024others(48): Show | 51 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.544-14262A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159290080 | ||||||
| chr4:159290125
|
C | T | 17 | a0001c0001t0002g0044a0001c0001t0002g0099a0001c0001t0006g0183others(14): Show | 17 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.544-14217C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159290125 | ||||||
| chr4:159290230
|
T | G | 129 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.544-14112T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159290230 | ||||||
| chr4:159290303
|
CTAAAGGC others(10): Show |
C | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-14036_544-1402 others(21): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159290303 | |||||
| chr4:159290361
|
C | T | 4 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0164others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-13981C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159290361 | ||||||
| chr4:159290599
|
A | G | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.544-13743A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159290599 | ||||||
| chr4:159290728
|
A | G | 1 | a0001c0001t0025g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.544-13614A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159290728 | ||||||
| chr4:159290754
|
CA | C | 6 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(3): Show | 6 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-13576delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159290754 | |||||
| chr4:159290967
|
C | A | 49 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(46): Show | 49 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.544-13375C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159290967 | ||||||
| chr4:159290991
|
A | G | 4 | a0001c0001t0002g0071a0001c0001t0011g0021a0001c0001t0011g0022others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-13351A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159290991 | ||||||
| chr4:159291186
|
A | G | 77 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.544-13156A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159291186 | ||||||
| chr4:159291331
|
T | C | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-13011T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159291331 | ||||||
| chr4:159291441
|
G | A | 1 | a0001c0002t0001g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.544-12901G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159291441 | ||||||
| chr4:159291449
|
T | C | 2 | a0001c0007t0016g0140a0001c0007t0016g0141 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.544-12893T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159291449 | ||||||
| chr4:159291751
|
A | G | 1 | a0001c0001t0006g0184 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.544-12591A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159291751 | ||||||
| chr4:159291786
|
G | GT | 28 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(25): Show | 28 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.544-12545dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159291786 | |||||
| chr4:159291786
|
GT | G | 46 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(43): Show | 46 | HG00099.hp1 HG00558.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.544-12545delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159291786 | |||||
| chr4:159291933
|
G | A | 1 | a0001c0001t0028g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.544-12409G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159291933 | ||||||
| chr4:159291958
|
C | T | 9 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0005g0092others(6): Show | 9 | HG02818.hp2 HG02922.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.544-12384C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159291958 | ||||||
| chr4:159292026
|
G | C | 1 | a0001c0002t0001g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.544-12316G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159292026 | ||||||
| chr4:159292388
|
T | C | 1 | a0001c0002t0003g0166 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.544-11954T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159292388 | ||||||
| chr4:159292416
|
G | A | 21 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0005g0092others(18): Show | 21 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.544-11926G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159292416 | ||||||
| chr4:159292418
|
A | C | 4 | a0001c0002t0001g0075a0001c0002t0001g0153a0001c0002t0001g0158others(1): Show | 4 | HG00597.hp1 HG01516.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-11924A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159292418 | ||||||
| chr4:159292429
|
C | T | 3 | a0001c0002t0001g0040a0001c0002t0001g0054a0001c0002t0001g0055 | 3 | HG00733.hp1 HG01109.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.544-11913C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159292429 | ||||||
| chr4:159292471
|
A | T | 130 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.544-11871A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159292471 | ||||||
| chr4:159292678
|
A | C | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.544-11664A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159292678 | ||||||
| chr4:159292788
|
G | A | 1 | a0001c0001t0008g0062 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.544-11554G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159292788 | ||||||
| chr4:159292809
|
T | C | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-11533T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159292809 | ||||||
| chr4:159292839
|
A | C | 5 | a0001c0001t0002g0149a0001c0001t0005g0024a0001c0001t0008g0062others(2): Show | 5 | HG00558.hp2 HG01943.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-11503A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159292839 | ||||||
| chr4:159292882
|
T | A | 45 | a0001c0001t0002g0060a0001c0001t0008g0033a0001c0001t0008g0041others(42): Show | 45 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.544-11460T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159292882 | ||||||
| chr4:159293153
|
T | G | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-11189T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159293153 | ||||||
| chr4:159293155
|
ATATAAT | A | 2 | a0001c0007t0016g0140a0001c0007t0016g0141 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.544-11184_544-1117 others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159293155 | |||||
| chr4:159293309
|
T | C | 1 | a0001c0002t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.544-11033T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159293309 | ||||||
| chr4:159293483
|
A | G | 1 | a0001c0001t0006g0177 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.544-10859A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159293483 | ||||||
| chr4:159293719
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.544-10623A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159293719 | ||||||
| chr4:159293920
|
G | T | 5 | a0001c0001t0002g0149a0001c0001t0005g0024a0001c0001t0008g0062others(2): Show | 5 | HG00558.hp2 HG01943.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-10422G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159293920 | ||||||
| chr4:159294063
|
T | C | 131 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.544-10279T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159294063 | ||||||
| chr4:159294113
|
T | C | 1 | a0001c0001t0004g0193 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.544-10229T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159294113 | ||||||
| chr4:159294230
|
T | A | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.544-10112T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159294230 | ||||||
| chr4:159294293
|
T | C | 1 | a0001c0002t0001g0107 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.544-10049T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159294293 | ||||||
| chr4:159294596
|
G | A | 1 | a0001c0002t0003g0160 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.544-9746G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159294596 | ||||||
| chr4:159294631
|
A | ATTCC | 3 | a0001c0001t0004g0193a0001c0001t0005g0049a0001c0002t0001g0107 | 3 | HG00738.hp2 NA18906.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.544-9709_544-9708i others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159294631 | |||||
| chr4:159294631
|
A | ATTCCTTC others(1): Show |
9 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0099others(6): Show | 9 | HG01069.hp1 HG02109.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.544-9709_544-9708i others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159294631 | |||||
| chr4:159294631
|
A | ATTCCTTC others(5): Show |
13 | a0001c0001t0006g0183a0001c0001t0006g0184a0001c0001t0024g0087others(10): Show | 13 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.544-9709_544-9708i others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159294631 | |||||
| chr4:159294631
|
A | ATTCCTTC others(9): Show |
10 | a0001c0001t0002g0079a0001c0002t0001g0018a0001c0002t0003g0168others(7): Show | 10 | HG01123.hp2 HG01517.hp2 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-9709_544-9708i others(18): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159294631 | |||||
| chr4:159294631
|
A | ATTCCTTC others(21): Show |
1 | a0001c0002t0003g0160 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.544-9709_544-9708i others(30): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159294631 | |||||
| chr4:159294631
|
ATTTC | A | 3 | a0001c0001t0009g0058a0001c0001t0009g0059a0001c0002t0001g0108 | 3 | HG00099.hp2 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.544-9708_544-9705d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159294631 | |||||
| chr4:159294634
|
T | C | 38 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(35): Show | 38 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.544-9708T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159294634 | ||||||
| chr4:159294634
|
T | TCTTC | 22 | a0001c0001t0002g0076a0001c0001t0002g0130a0001c0001t0002g0132others(19): Show | 22 | HG01884.hp1 HG01884.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.544-9655_544-9652d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159294634 | |||||
| chr4:159294634
|
T | TCTTCCTT others(1): Show |
18 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0029others(15): Show | 18 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.544-9659_544-9652d others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159294634 | |||||
| chr4:159294634
|
T | TCTTCCTT others(5): Show |
15 | a0001c0001t0002g0015a0001c0001t0002g0057a0001c0001t0002g0088others(12): Show | 15 | HG00280.hp1 HG00639.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.544-9663_544-9652d others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159294634 | |||||
| chr4:159294634
|
T | TCTTCCTT others(9): Show |
7 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0097others(4): Show | 7 | HG00558.hp1 HG01074.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.544-9667_544-9652d others(18): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159294634 | |||||
| chr4:159294634
|
T | TCTTCCTT others(13): Show |
2 | a0001c0001t0002g0145a0001c0002t0001g0013 | 2 | HG00733.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.544-9671_544-9652d others(22): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159294634 | |||||
| chr4:159294634
|
T | TCTTCCTT others(17): Show |
2 | a0001c0002t0001g0102a0001c0008t0002g0119 | 2 | HG01071.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.544-9675_544-9652d others(26): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159294634 | |||||
| chr4:159294634
|
TCTTC | T | 23 | a0001c0001t0002g0010a0001c0001t0002g0096a0001c0001t0002g0142others(20): Show | 23 | HG00639.hp1 HG00642.hp2 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.544-9655_544-9652d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159294634 | |||||
| chr4:159294634
|
TCTTCCTT others(1): Show |
T | 9 | a0001c0001t0004g0194a0001c0001t0005g0086a0001c0001t0005g0092others(6): Show | 9 | HG00597.hp1 HG01516.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.544-9659_544-9652d others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159294634 | |||||
| chr4:159294634
|
TCTTCCTT others(5): Show |
T | 13 | a0001c0001t0005g0051a0001c0001t0008g0067a0001c0002t0001g0153others(10): Show | 13 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.544-9663_544-9652d others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159294634 | |||||
| chr4:159294634
|
TCTTCCTT others(9): Show |
T | 8 | a0001c0001t0002g0149a0001c0001t0005g0024a0001c0001t0008g0062others(5): Show | 8 | HG00558.hp2 HG01943.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-9667_544-9652d others(18): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159294634 | |||||
| chr4:159294634
|
TCTTCCTT others(13): Show |
T | 3 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0005t0012g0105 | 3 | HG02559.hp2 HG02647.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.544-9671_544-9652d others(22): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159294634 | |||||
| chr4:159294634
|
TCTTCCTT others(17): Show |
T | 1 | a0001c0003t0004g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.544-9675_544-9652d others(26): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159294634 | |||||
| chr4:159294708
|
G | A | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-9634G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159294708 | ||||||
| chr4:159294839
|
C | A | 1 | a0001c0002t0001g0034 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.544-9503C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159294839 | ||||||
| chr4:159294849
|
C | T | 1 | a0001c0001t0031g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.544-9493C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159294849 | ||||||
| chr4:159294850
|
G | A | 12 | a0001c0003t0004g0009a0001c0003t0004g0019a0001c0003t0004g0045others(9): Show | 12 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.544-9492G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159294850 | ||||||
| chr4:159294899
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.544-9443G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159294899 | ||||||
| chr4:159294916
|
T | C | 129 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.544-9426T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159294916 | ||||||
| chr4:159294952
|
C | G | 1 | a0001c0002t0003g0169 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.544-9390C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159294952 | ||||||
| chr4:159295010
|
A | T | 1 | a0001c0001t0008g0041 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.544-9332A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295010 | ||||||
| chr4:159295089
|
A | G | 188 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(185): Show | 188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.544-9253A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295089 | ||||||
| chr4:159295135
|
T | C | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-9207T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295135 | ||||||
| chr4:159295207
|
C | T | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.544-9135C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295207 | ||||||
| chr4:159295351
|
T | G | 3 | a0001c0002t0001g0040a0001c0002t0001g0054a0001c0002t0001g0055 | 3 | HG00733.hp1 HG01109.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.544-8991T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295351 | ||||||
| chr4:159295575
|
A | G | 1 | a0001c0002t0001g0048 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.544-8767A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295575 | ||||||
| chr4:159295720
|
A | AGT | 13 | a0001c0001t0002g0088a0001c0001t0002g0130a0001c0001t0009g0035others(10): Show | 13 | HG00280.hp1 HG02258.hp1 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.544-8588_544-8587d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295720 | |||||
| chr4:159295720
|
A | AGTGT | 12 | a0001c0001t0002g0099a0001c0001t0006g0183a0001c0002t0001g0027others(9): Show | 12 | HG00735.hp1 HG01071.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.544-8590_544-8587d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295720 | |||||
| chr4:159295720
|
A | AGTGTGT | 5 | a0001c0001t0002g0044a0001c0001t0004g0193a0001c0001t0006g0163others(2): Show | 5 | HG01069.hp1 HG02129.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-8592_544-8587d others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295720 | |||||
| chr4:159295720
|
A | AGTGTGTG others(1): Show |
3 | a0001c0001t0006g0184a0001c0002t0003g0179a0001c0002t0003g0182 | 3 | HG01106.hp1 HG02451.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.544-8594_544-8587d others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295720 | |||||
| chr4:159295720
|
AGT | A | 16 | a0001c0001t0002g0015a0001c0001t0002g0060a0001c0001t0002g0074others(13): Show | 16 | HG00438.hp2 HG00558.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.544-8588_544-8587d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295720 | |||||
| chr4:159295720
|
AGTGT | A | 11 | a0001c0001t0010g0162a0001c0002t0001g0014a0001c0002t0001g0030others(8): Show | 11 | HG00639.hp1 HG00733.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-8590_544-8587d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295720 | |||||
| chr4:159295720
|
AGTGTGTG others(1): Show |
A | 5 | a0001c0001t0002g0149a0001c0001t0008g0067a0001c0001t0008g0112others(2): Show | 5 | HG00558.hp2 HG01099.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.544-8594_544-8587d others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295720 | |||||
| chr4:159295720
|
AGTGTGTG others(3): Show |
A | 2 | a0001c0001t0005g0024a0001c0001t0008g0062 | 2 | HG02717.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.544-8596_544-8587d others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295720 | |||||
| chr4:159295722
|
T | A | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.544-8620T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295722 | ||||||
| chr4:159295740
|
TGTGTGTG others(13): Show |
T | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.544-8600_544-8581d others(22): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295740 | |||||
| chr4:159295744
|
T | C | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-8598T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295744 | ||||||
| chr4:159295744
|
TGTGTGTG others(9): Show |
T | 2 | a0001c0002t0003g0150a0001c0002t0003g0176 | 2 | HG01261.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.544-8596_544-8581d others(18): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295744 | |||||
| chr4:159295744
|
TGTGTGTG others(11): Show |
T | 1 | a0001c0010t0002g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.544-8596_544-8579d others(20): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295744 | |||||
| chr4:159295746
|
T | C | 5 | a0001c0001t0008g0033a0001c0001t0008g0041a0001c0001t0011g0021others(2): Show | 5 | HG01993.hp2 HG02145.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.544-8596T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295746 | ||||||
| chr4:159295746
|
TGTGTGTG others(3): Show |
T | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-8594_544-8585d others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295746 | |||||
| chr4:159295746
|
TGTGTGTG others(9): Show |
T | 1 | a0001c0002t0001g0158 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.544-8594_544-8579d others(18): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295746 | |||||
| chr4:159295746
|
TGTGTGTG others(11): Show |
T | 1 | a0001c0002t0001g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.544-8594_544-8577d others(20): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295746 | |||||
| chr4:159295748
|
T | C | 15 | a0001c0001t0002g0060a0001c0001t0008g0033a0001c0001t0008g0041others(12): Show | 15 | HG00438.hp2 HG00733.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.544-8594T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295748 | ||||||
| chr4:159295748
|
T | TGC | 2 | a0001c0002t0001g0128a0001c0002t0001g0139 | 2 | HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.544-8593_544-8592i others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295748 | |||||
| chr4:159295748
|
TGTGTGTG others(1): Show |
T | 4 | a0001c0001t0006g0175a0001c0001t0015g0190a0001c0001t0015g0191others(1): Show | 4 | HG01099.hp2 HG01891.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-8592_544-8585d others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295748 | |||||
| chr4:159295750
|
T | C | 34 | a0001c0001t0002g0060a0001c0001t0008g0033a0001c0001t0008g0041others(31): Show | 34 | HG00438.hp2 HG00639.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.544-8592T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295750 | ||||||
| chr4:159295750
|
T | TGC | 2 | a0001c0001t0002g0071a0001c0004t0003g0159 | 2 | HG00280.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.544-8591_544-8590i others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295750 | |||||
| chr4:159295752
|
T | C | 42 | a0001c0001t0002g0060a0001c0001t0002g0071a0001c0001t0002g0118others(39): Show | 42 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.544-8590T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295752 | ||||||
| chr4:159295752
|
TGTGC | T | 4 | a0001c0001t0002g0005a0001c0001t0010g0155a0001c0001t0010g0164others(1): Show | 4 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-8588_544-8585d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295752 | |||||
| chr4:159295754
|
T | C | 52 | a0001c0001t0002g0015a0001c0001t0002g0060a0001c0001t0002g0066others(49): Show | 52 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.544-8588T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295754 | ||||||
| chr4:159295754
|
T | TGC | 11 | a0001c0001t0002g0029a0001c0001t0002g0091a0001c0001t0002g0098others(8): Show | 11 | HG00642.hp1 HG00738.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.544-8569_544-8568d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295754 | |||||
| chr4:159295754
|
T | TGTGC | 3 | a0001c0001t0002g0154a0001c0002t0001g0034a0001c0002t0001g0038 | 3 | HG00738.hp1 HG01069.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.544-8587_544-8586i others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295754 | |||||
| chr4:159295754
|
TGC | T | 6 | a0001c0001t0009g0059a0001c0001t0025g0081a0001c0002t0001g0108others(3): Show | 6 | HG00099.hp2 HG01884.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.544-8569_544-8568d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295754 | |||||
| chr4:159295754
|
TGCGC | T | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.544-8571_544-8568d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295754 | |||||
| chr4:159295754
|
TGCGCGC | T | 8 | a0001c0001t0004g0194a0001c0001t0005g0092a0001c0001t0005g0093others(5): Show | 8 | HG02145.hp1 HG02976.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.544-8573_544-8568d others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295754 | |||||
| chr4:159295754
|
TGCGCGCG others(1): Show |
T | 16 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0013g0083others(13): Show | 16 | HG02055.hp1 HG02109.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.544-8575_544-8568d others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295754 | |||||
| chr4:159295754
|
TGCGCGCG others(3): Show |
T | 4 | a0001c0001t0026g0003a0001c0003t0004g0019a0001c0003t0017g0117others(1): Show | 4 | HG01081.hp2 HG02922.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-8577_544-8568d others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159295754 | |||||
| chr4:159295756
|
C | T | 30 | a0001c0001t0002g0044a0001c0001t0002g0076a0001c0001t0004g0193others(27): Show | 30 | HG00099.hp1 HG01069.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.544-8586C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295756 | ||||||
| chr4:159295758
|
C | T | 2 | a0001c0001t0009g0059a0001c0002t0001g0108 | 2 | HG00099.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.544-8584C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295758 | ||||||
| chr4:159295760
|
C | T | 1 | a0001c0001t0009g0059 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.544-8582C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295760 | ||||||
| chr4:159295761
|
G | C | 1 | a0001c0002t0001g0054 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.544-8581G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295761 | ||||||
| chr4:159295762
|
C | T | 9 | a0001c0001t0005g0092a0001c0001t0005g0093a0001c0001t0008g0070others(6): Show | 9 | HG01993.hp2 HG02145.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.544-8580C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295762 | ||||||
| chr4:159295764
|
C | T | 22 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0005g0092others(19): Show | 22 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.544-8578C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295764 | ||||||
| chr4:159295768
|
C | T | 1 | a0001c0002t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.544-8574C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295768 | ||||||
| chr4:159295831
|
G | T | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-8511G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295831 | ||||||
| chr4:159295975
|
G | A | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.544-8367G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159295975 | ||||||
| chr4:159296049
|
T | TA | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.544-8291dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159296049 | |||||
| chr4:159296069
|
G | A | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-8273G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159296069 | ||||||
| chr4:159296127
|
A | G | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.544-8215A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159296127 | ||||||
| chr4:159296354
|
T | A | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-7988T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159296354 | ||||||
| chr4:159296516
|
C | T | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.544-7826C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159296516 | ||||||
| chr4:159296583
|
T | A | 1 | a0001c0002t0001g0052 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.544-7759T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159296583 | ||||||
| chr4:159296747
|
G | A | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.544-7595G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159296747 | ||||||
| chr4:159296809
|
C | A | 128 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(125): Show | 128 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.544-7533C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159296809 | ||||||
| chr4:159296920
|
A | G | 9 | a0001c0003t0004g0009a0001c0003t0004g0045a0001c0003t0004g0047others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.544-7422A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159296920 | ||||||
| chr4:159296966
|
TATTG | T | 5 | a0001c0001t0002g0149a0001c0001t0005g0024a0001c0001t0008g0062others(2): Show | 5 | HG00558.hp2 HG01943.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-7372_544-7369d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159296966 | |||||
| chr4:159296999
|
A | G | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.544-7343A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159296999 | ||||||
| chr4:159297021
|
T | C | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-7321T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159297021 | ||||||
| chr4:159297108
|
T | C | 9 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0005g0092others(6): Show | 9 | HG02818.hp2 HG02922.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.544-7234T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159297108 | ||||||
| chr4:159297401
|
A | G | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-6941A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159297401 | ||||||
| chr4:159297469
|
T | A | 1 | a0001c0002t0001g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.544-6873T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159297469 | ||||||
| chr4:159297483
|
A | C | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.544-6859A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159297483 | ||||||
| chr4:159297660
|
A | AC | 77 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.544-6681dupC | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159297660 | |||||
| chr4:159297672
|
G | T | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.544-6670G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159297672 | ||||||
| chr4:159297821
|
G | A | 5 | a0001c0002t0001g0128a0001c0002t0001g0129a0001c0002t0001g0138others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-6521G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159297821 | ||||||
| chr4:159298245
|
A | G | 49 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.544-6097A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159298245 | ||||||
| chr4:159298336
|
G | A | 1 | a0001c0002t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.544-6006G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159298336 | ||||||
| chr4:159298341
|
G | T | 1 | a0001c0001t0002g0118 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.544-6001G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159298341 | ||||||
| chr4:159298697
|
G | A | 1 | a0001c0001t0031g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.544-5645G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159298697 | ||||||
| chr4:159299430
|
T | TA | 10 | a0001c0001t0002g0154a0001c0001t0006g0175a0001c0001t0007g0077others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.544-4898dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159299430 | |||||
| chr4:159299430
|
T | TAA | 42 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(39): Show | 42 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.544-4899_544-4898d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159299430 | |||||
| chr4:159299556
|
C | T | 1 | a0001c0002t0003g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.544-4786C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159299556 | ||||||
| chr4:159299557
|
G | A | 1 | a0001c0001t0028g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.544-4785G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159299557 | ||||||
| chr4:159299582
|
C | T | 2 | a0001c0001t0002g0060a0001c0010t0002g0065 | 2 | HG00438.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.544-4760C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159299582 | ||||||
| chr4:159299631
|
CT | C | 4 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0164others(1): Show | 4 | HG02615.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-4702delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159299631 | |||||
| chr4:159299640
|
T | A | 9 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.544-4702T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159299640 | ||||||
| chr4:159299791
|
A | C | 5 | a0001c0001t0002g0149a0001c0001t0005g0024a0001c0001t0008g0062others(2): Show | 5 | HG00558.hp2 HG01943.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-4551A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159299791 | ||||||
| chr4:159300176
|
TTATA | T | 2 | a0001c0001t0002g0060a0001c0010t0002g0065 | 2 | HG00438.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.544-4162_544-4159d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159300176 | |||||
| chr4:159300218
|
CAA | C | 43 | a0001c0001t0002g0060a0001c0001t0008g0033a0001c0001t0008g0041others(40): Show | 43 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.544-4123_544-4122d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159300218 | ||||||
| chr4:159300282
|
G | A | 9 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0005g0092others(6): Show | 9 | HG02818.hp2 HG02922.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.544-4060G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159300282 | ||||||
| chr4:159300364
|
A | G | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.544-3978A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159300364 | ||||||
| chr4:159300440
|
G | A | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.544-3902G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159300440 | ||||||
| chr4:159300484
|
G | A | 3 | a0001c0002t0001g0030a0001c0002t0001g0031a0001c0002t0001g0043 | 3 | HG00639.hp1 HG01074.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.544-3858G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159300484 | ||||||
| chr4:159300648
|
GA | G | 50 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.544-3692delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159300648 | |||||
| chr4:159300688
|
T | C | 1 | a0001c0001t0002g0154 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.544-3654T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159300688 | ||||||
| chr4:159300726
|
G | A | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.544-3616G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159300726 | ||||||
| chr4:159300741
|
A | C | 1 | a0001c0003t0004g0080 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.544-3601A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159300741 | ||||||
| chr4:159300798
|
G | C | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-3544G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159300798 | ||||||
| chr4:159300812
|
T | C | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.544-3530T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159300812 | ||||||
| chr4:159300860
|
T | C | 1 | a0001c0010t0002g0065 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.544-3482T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159300860 | ||||||
| chr4:159300929
|
C | T | 50 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.544-3413C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159300929 | ||||||
| chr4:159300933
|
A | G | 1 | a0001c0001t0009g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.544-3409A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159300933 | ||||||
| chr4:159300958
|
C | T | 5 | a0001c0001t0002g0149a0001c0001t0005g0024a0001c0001t0008g0062others(2): Show | 5 | HG00558.hp2 HG01943.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-3384C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159300958 | ||||||
| chr4:159300977
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.544-3365C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159300977 | ||||||
| chr4:159301218
|
G | A | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.544-3124G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159301218 | ||||||
| chr4:159301241
|
C | T | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.544-3101C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159301241 | ||||||
| chr4:159301395
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.544-2947A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159301395 | ||||||
| chr4:159301491
|
A | G | 1 | a0001c0001t0025g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.544-2851A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159301491 | ||||||
| chr4:159301635
|
A | G | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-2707A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159301635 | ||||||
| chr4:159301911
|
T | A | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.544-2431T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159301911 | ||||||
| chr4:159301911
|
T | C | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.544-2431T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159301911 | ||||||
| chr4:159301936
|
G | A | 1 | a0001c0001t0005g0049 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.544-2406G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159301936 | ||||||
| chr4:159302051
|
C | T | 2 | a0001c0001t0008g0070a0001c0005t0005g0016 | 2 | HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.544-2291C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159302051 | ||||||
| chr4:159302177
|
C | T | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.544-2165C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159302177 | ||||||
| chr4:159302338
|
A | AT | 127 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(124): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.544-1997dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159302338 | |||||
| chr4:159302345
|
T | A | 1 | a0001c0001t0006g0187 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.544-1997T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159302345 | ||||||
| chr4:159302739
|
G | T | 41 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.544-1603G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159302739 | ||||||
| chr4:159302768
|
T | A | 49 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.544-1574T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159302768 | ||||||
| chr4:159302768
|
T | C | 12 | a0001c0003t0004g0009a0001c0003t0004g0019a0001c0003t0004g0045others(9): Show | 12 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.544-1574T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159302768 | ||||||
| chr4:159302853
|
C | T | 41 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.544-1489C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159302853 | ||||||
| chr4:159302919
|
C | T | 1 | a0001c0001t0006g0163 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.544-1423C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159302919 | ||||||
| chr4:159303016
|
C | T | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.544-1326C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159303016 | ||||||
| chr4:159303175
|
C | T | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.544-1167C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159303175 | ||||||
| chr4:159303202
|
T | A | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.544-1140T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159303202 | ||||||
| chr4:159303362
|
G | T | 12 | a0001c0003t0004g0009a0001c0003t0004g0019a0001c0003t0004g0045others(9): Show | 12 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.544-980G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159303362 | ||||||
| chr4:159303478
|
A | C | 9 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0005g0092others(6): Show | 9 | HG02818.hp2 HG02922.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.544-864A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159303478 | ||||||
| chr4:159303488
|
C | T | 131 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(128): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.544-854C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159303488 | ||||||
| chr4:159303532
|
A | G | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-810A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159303532 | ||||||
| chr4:159303639
|
G | GT | 30 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(27): Show | 30 | HG01081.hp2 HG01261.hp2 HG01978.hp1 others(27): Show |
intron_variant | MODIFIER | c.544-692dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | INFO_REALIGN_3_PRIME | chr4 | 159303639 | |||||
| chr4:159303803
|
A | C | 1 | a0001c0002t0003g0169 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.544-539A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159303803 | ||||||
| chr4:159303955
|
T | C | 3 | a0001c0001t0002g0089a0001c0001t0002g0131a0001c0001t0006g0187 | 3 | HG00597.hp2 HG02074.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.544-387T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159303955 | ||||||
| chr4:159304037
|
T | C | 2 | a0001c0001t0002g0079a0001c0002t0001g0034 | 2 | HG00738.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.544-305T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159304037 | ||||||
| chr4:159304115
|
A | G | 1 | a0001c0001t0002g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.544-227A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159304115 | ||||||
| chr4:159304184
|
G | T | 128 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(125): Show | 128 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.544-158G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159304184 | ||||||
| chr4:159304241
|
G | T | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.544-101G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159304241 | ||||||
| chr4:159304278
|
T | A | 45 | a0001c0001t0002g0060a0001c0001t0008g0033a0001c0001t0008g0041others(42): Show | 45 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.544-64T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 7/29 | chr4 | 159304278 | ||||||
| chr4:159304674
|
C | T | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.675+201C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159304674 | ||||||
| chr4:159304690
|
TC | T | 5 | a0001c0001t0002g0149a0001c0001t0005g0024a0001c0001t0008g0062others(2): Show | 5 | HG00558.hp2 HG01943.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.675+219delC | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr4 | 159304690 | |||||
| chr4:159304783
|
A | T | 1 | a0001c0006t0014g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.675+310A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159304783 | ||||||
| chr4:159304847
|
G | A | 4 | a0001c0001t0002g0071a0001c0001t0011g0021a0001c0001t0011g0022others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+374G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159304847 | ||||||
| chr4:159305107
|
T | G | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.675+634T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159305107 | ||||||
| chr4:159305199
|
C | T | 1 | a0001c0001t0009g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.675+726C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159305199 | ||||||
| chr4:159305289
|
A | G | 1 | a0001c0002t0001g0053 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.675+816A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159305289 | ||||||
| chr4:159305333
|
C | T | 4 | a0001c0001t0002g0079a0001c0002t0001g0034a0001c0002t0003g0136others(1): Show | 4 | HG00738.hp1 HG01123.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+860C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159305333 | ||||||
| chr4:159305339
|
C | G | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.675+866C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159305339 | ||||||
| chr4:159305430
|
C | T | 136 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(133): Show | 136 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.675+957C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159305430 | ||||||
| chr4:159305520
|
A | G | 1 | a0001c0001t0002g0060 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.675+1047A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159305520 | ||||||
| chr4:159305530
|
A | T | 128 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(125): Show | 128 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.675+1057A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159305530 | ||||||
| chr4:159305591
|
G | A | 43 | a0001c0001t0002g0060a0001c0001t0008g0033a0001c0001t0008g0041others(40): Show | 43 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.675+1118G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159305591 | ||||||
| chr4:159305744
|
G | C | 192 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.675+1271G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159305744 | ||||||
| chr4:159305883
|
C | T | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.675+1410C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159305883 | ||||||
| chr4:159305958
|
G | A | 40 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(37): Show | 40 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.675+1485G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159305958 | ||||||
| chr4:159306141
|
A | AT | 43 | a0001c0001t0002g0060a0001c0001t0008g0033a0001c0001t0008g0041others(40): Show | 43 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.675+1678dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr4 | 159306141 | |||||
| chr4:159306253
|
A | G | 1 | a0001c0001t0002g0142 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.675+1780A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159306253 | ||||||
| chr4:159306446
|
A | G | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.675+1973A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159306446 | ||||||
| chr4:159306520
|
A | G | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.675+2047A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159306520 | ||||||
| chr4:159306677
|
G | A | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.675+2204G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159306677 | ||||||
| chr4:159306870
|
G | T | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.675+2397G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159306870 | ||||||
| chr4:159306939
|
T | TC | 192 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(189): Show | 192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.675+2467dupC | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr4 | 159306939 | |||||
| chr4:159306973
|
G | T | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.675+2500G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159306973 | ||||||
| chr4:159307165
|
C | T | 5 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0164others(2): Show | 5 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.675+2692C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159307165 | ||||||
| chr4:159307251
|
T | G | 1 | a0001c0001t0002g0125 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.675+2778T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159307251 | ||||||
| chr4:159307330
|
A | C | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.675+2857A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159307330 | ||||||
| chr4:159307784
|
C | T | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.675+3311C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159307784 | ||||||
| chr4:159307848
|
A | C | 1 | a0001c0001t0007g0094 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.675+3375A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159307848 | ||||||
| chr4:159307850
|
A | G | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.675+3377A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159307850 | ||||||
| chr4:159307935
|
C | T | 27 | a0001c0001t0002g0044a0001c0001t0002g0099a0001c0001t0004g0193others(24): Show | 27 | HG00099.hp1 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.675+3462C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159307935 | ||||||
| chr4:159307966
|
G | A | 8 | a0001c0001t0002g0025a0001c0001t0005g0049a0001c0001t0009g0058others(5): Show | 8 | HG01981.hp1 HG03540.hp2 NA18955.hp1 others(5): Show |
intron_variant | MODIFIER | c.675+3493G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159307966 | ||||||
| chr4:159308284
|
C | T | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.675+3811C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159308284 | ||||||
| chr4:159308516
|
T | C | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.675+4043T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159308516 | ||||||
| chr4:159309213
|
C | G | 1 | a0001c0002t0001g0018 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.675+4740C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159309213 | ||||||
| chr4:159309276
|
T | C | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.675+4803T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159309276 | ||||||
| chr4:159309889
|
A | G | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.676-4702A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159309889 | ||||||
| chr4:159309993
|
A | ATAAAACA others(17): Show |
27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.676-4598_676-4597i others(26): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159309993 | ||||||
| chr4:159309995
|
G | A | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.676-4596G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159309995 | ||||||
| chr4:159309996
|
G | A | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.676-4595G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159309996 | ||||||
| chr4:159309999
|
C | A | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.676-4592C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159309999 | ||||||
| chr4:159310030
|
T | C | 1 | a0001c0002t0001g0052 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.676-4561T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159310030 | ||||||
| chr4:159310251
|
A | T | 40 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(37): Show | 40 | HG00099.hp1 HG00735.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.676-4340A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159310251 | ||||||
| chr4:159310275
|
A | G | 1 | a0001c0001t0028g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.676-4316A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159310275 | ||||||
| chr4:159310283
|
C | G | 1 | a0001c0001t0002g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.676-4308C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159310283 | ||||||
| chr4:159310592
|
T | A | 1 | a0001c0001t0031g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.676-3999T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159310592 | ||||||
| chr4:159310642
|
TATCACTA | T | 50 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.676-3948_676-3942d others(9): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159310642 | ||||||
| chr4:159310802
|
C | T | 1 | a0001c0002t0003g0180 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.676-3789C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159310802 | ||||||
| chr4:159310984
|
T | TTCAATTT others(308): Show |
1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.676-3594_676-3593i others(317): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr4 | 159310984 | |||||
| chr4:159310988
|
AT | A | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.676-3594delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr4 | 159310988 | |||||
| chr4:159311086
|
T | C | 1 | a0001c0002t0001g0108 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.676-3505T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159311086 | ||||||
| chr4:159311101
|
T | G | 1 | a0001c0001t0002g0131 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.676-3490T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159311101 | ||||||
| chr4:159311251
|
A | T | 45 | a0001c0001t0002g0060a0001c0001t0008g0033a0001c0001t0008g0041others(42): Show | 45 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.676-3340A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159311251 | ||||||
| chr4:159311368
|
G | A | 4 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0164others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-3223G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159311368 | ||||||
| chr4:159311767
|
A | G | 51 | a0001c0001t0002g0060a0001c0001t0002g0149a0001c0001t0005g0024others(48): Show | 51 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(48): Show |
intron_variant | MODIFIER | c.676-2824A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159311767 | ||||||
| chr4:159311838
|
G | A | 1 | a0001c0002t0001g0040 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.676-2753G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159311838 | ||||||
| chr4:159312063
|
T | C | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.676-2528T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159312063 | ||||||
| chr4:159312080
|
C | A | 129 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.676-2511C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159312080 | ||||||
| chr4:159312140
|
A | G | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.676-2451A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159312140 | ||||||
| chr4:159312161
|
G | C | 1 | a0001c0002t0003g0008 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.676-2430G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159312161 | ||||||
| chr4:159312282
|
A | T | 49 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(46): Show | 49 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.676-2309A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159312282 | ||||||
| chr4:159312668
|
T | G | 43 | a0001c0001t0002g0060a0001c0001t0008g0033a0001c0001t0008g0041others(40): Show | 43 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.676-1923T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159312668 | ||||||
| chr4:159312752
|
A | T | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.676-1839A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159312752 | ||||||
| chr4:159312874
|
G | A | 1 | a0001c0001t0021g0028 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.676-1717G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159312874 | ||||||
| chr4:159312899
|
G | A | 1 | a0001c0001t0002g0118 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.676-1692G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159312899 | ||||||
| chr4:159312977
|
G | A | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.676-1614G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159312977 | ||||||
| chr4:159312993
|
C | T | 1 | a0001c0001t0002g0005 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.676-1598C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159312993 | ||||||
| chr4:159313103
|
G | A | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-1488G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159313103 | ||||||
| chr4:159313158
|
AAAAG | A | 41 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(38): Show | 41 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.676-1421_676-1418d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr4 | 159313158 | |||||
| chr4:159313163
|
A | G | 1 | a0001c0002t0003g0166 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.676-1428A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159313163 | ||||||
| chr4:159313304
|
A | G | 1 | a0001c0001t0002g0001 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.676-1287A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159313304 | ||||||
| chr4:159313353
|
C | T | 1 | a0001c0002t0001g0052 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.676-1238C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159313353 | ||||||
| chr4:159313506
|
C | T | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.676-1085C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159313506 | ||||||
| chr4:159313544
|
ATC | A | 3 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0003g0186 | 3 | HG01516.hp2 HG01517.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.676-1045_676-1044d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr4 | 159313544 | |||||
| chr4:159314067
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.676-524A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159314067 | ||||||
| chr4:159314298
|
A | G | 2 | a0001c0001t0002g0066a0001c0001t0002g0132 | 2 | HG03239.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.676-293A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159314298 | ||||||
| chr4:159314323
|
A | G | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.676-268A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 8/29 | chr4 | 159314323 | ||||||
| chr4:159315036
|
CA | C | 106 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(103): Show | 106 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.853+281delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr4 | 159315036 | |||||
| chr4:159315095
|
G | A | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.853+327G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159315095 | ||||||
| chr4:159315309
|
T | A | 1 | a0001c0002t0001g0018 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.853+541T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159315309 | ||||||
| chr4:159315310
|
T | A | 78 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.853+542T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159315310 | ||||||
| chr4:159315348
|
T | G | 1 | a0001c0001t0028g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.853+580T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159315348 | ||||||
| chr4:159315353
|
C | T | 1 | a0001c0001t0013g0084 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.853+585C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159315353 | ||||||
| chr4:159315390
|
A | T | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.853+622A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159315390 | ||||||
| chr4:159315391
|
T | TTA | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.853+625_853+626dup others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr4 | 159315391 | |||||
| chr4:159315482
|
G | T | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.853+714G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159315482 | ||||||
| chr4:159315845
|
A | C | 4 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0164others(1): Show | 4 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.853+1077A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159315845 | ||||||
| chr4:159315851
|
A | G | 51 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.853+1083A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159315851 | ||||||
| chr4:159315991
|
A | G | 1 | a0001c0001t0009g0146 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.853+1223A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159315991 | ||||||
| chr4:159316055
|
C | G | 8 | a0001c0003t0004g0009a0001c0003t0004g0047a0001c0003t0004g0061others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.853+1287C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159316055 | ||||||
| chr4:159316374
|
A | G | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.853+1606A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159316374 | ||||||
| chr4:159316752
|
G | A | 193 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.853+1984G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159316752 | ||||||
| chr4:159317153
|
A | T | 1 | a0001c0001t0002g0060 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.853+2385A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159317153 | ||||||
| chr4:159317186
|
A | C | 3 | a0001c0002t0001g0013a0001c0002t0001g0102a0002c0009t0002g0011 | 3 | HG01071.hp1 HG01258.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.853+2418A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159317186 | ||||||
| chr4:159317308
|
C | T | 1 | a0001c0002t0001g0102 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.853+2540C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159317308 | ||||||
| chr4:159317608
|
C | T | 1 | a0001c0002t0003g0169 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.853+2840C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159317608 | ||||||
| chr4:159318045
|
A | G | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.853+3277A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159318045 | ||||||
| chr4:159318057
|
T | TA | 28 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(25): Show | 28 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.853+3301dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr4 | 159318057 | |||||
| chr4:159318127
|
G | A | 5 | a0001c0001t0002g0149a0001c0001t0005g0024a0001c0001t0008g0062others(2): Show | 5 | HG00558.hp2 HG01943.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.853+3359G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159318127 | ||||||
| chr4:159318224
|
G | A | 77 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0079others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.853+3456G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159318224 | ||||||
| chr4:159318229
|
A | G | 2 | a0001c0001t0002g0154a0001c0001t0005g0086 | 2 | HG03098.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.853+3461A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159318229 | ||||||
| chr4:159318293
|
T | C | 43 | a0001c0001t0002g0060a0001c0001t0008g0033a0001c0001t0008g0041others(40): Show | 43 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.853+3525T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159318293 | ||||||
| chr4:159318299
|
T | C | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.853+3531T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159318299 | ||||||
| chr4:159318370
|
A | G | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.853+3602A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159318370 | ||||||
| chr4:159318448
|
A | T | 1 | a0001c0002t0001g0152 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.853+3680A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159318448 | ||||||
| chr4:159318670
|
G | A | 1 | a0001c0002t0003g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.854-3677G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159318670 | ||||||
| chr4:159318674
|
T | A | 1 | a0001c0001t0008g0070 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.854-3673T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159318674 | ||||||
| chr4:159318675
|
A | T | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.854-3672A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159318675 | ||||||
| chr4:159318680
|
A | T | 17 | a0001c0001t0002g0149a0001c0001t0005g0024a0001c0001t0008g0062others(14): Show | 17 | HG00558.hp2 HG01081.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.854-3667A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159318680 | ||||||
| chr4:159318693
|
T | G | 1 | a0001c0002t0001g0037 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.854-3654T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159318693 | ||||||
| chr4:159318843
|
T | C | 1 | a0001c0002t0001g0128 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.854-3504T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159318843 | ||||||
| chr4:159319133
|
GTC | G | 3 | a0001c0001t0002g0005a0001c0007t0016g0140a0001c0007t0016g0141 | 3 | HG01884.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.854-3213_854-3212d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159319133 | ||||||
| chr4:159319233
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.854-3114G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159319233 | ||||||
| chr4:159319747
|
T | C | 129 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.854-2600T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159319747 | ||||||
| chr4:159319769
|
G | GT | 5 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(2): Show | 5 | HG02155.hp2 HG02559.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.854-2568dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr4 | 159319769 | |||||
| chr4:159319853
|
A | C | 1 | a0001c0002t0001g0138 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.854-2494A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159319853 | ||||||
| chr4:159319854
|
C | T | 1 | a0001c0001t0002g0089 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.854-2493C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159319854 | ||||||
| chr4:159320122
|
A | G | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.854-2225A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159320122 | ||||||
| chr4:159320132
|
A | G | 5 | a0001c0001t0002g0149a0001c0001t0005g0024a0001c0001t0008g0062others(2): Show | 5 | HG00558.hp2 HG01943.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.854-2215A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159320132 | ||||||
| chr4:159320142
|
G | A | 2 | a0001c0001t0002g0088a0001c0001t0002g0097 | 2 | HG00280.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.854-2205G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159320142 | ||||||
| chr4:159320267
|
A | G | 1 | a0001c0001t0002g0074 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.854-2080A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159320267 | ||||||
| chr4:159320354
|
A | G | 1 | a0001c0001t0002g0130 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.854-1993A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159320354 | ||||||
| chr4:159320669
|
C | T | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.854-1678C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159320669 | ||||||
| chr4:159321108
|
A | C | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.854-1239A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159321108 | ||||||
| chr4:159321122
|
A | G | 1 | a0001c0001t0028g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.854-1225A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159321122 | ||||||
| chr4:159321135
|
T | C | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.854-1212T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159321135 | ||||||
| chr4:159321204
|
CT | C | 83 | a0001c0001t0002g0060a0001c0001t0002g0098a0001c0001t0002g0110others(80): Show | 83 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.854-1125delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr4 | 159321204 | |||||
| chr4:159321204
|
CTT | C | 51 | a0001c0001t0002g0025a0001c0001t0002g0079a0001c0001t0002g0099others(48): Show | 51 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.854-1126_854-1125d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr4 | 159321204 | |||||
| chr4:159321340
|
A | G | 27 | a0001c0001t0004g0194a0001c0001t0005g0012a0001c0001t0005g0051others(24): Show | 27 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.854-1007A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159321340 | ||||||
| chr4:159321353
|
C | T | 1 | a0001c0002t0003g0166 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.854-994C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159321353 | ||||||
| chr4:159321399
|
G | A | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.854-948G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159321399 | ||||||
| chr4:159321447
|
A | G | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.854-900A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159321447 | ||||||
| chr4:159321625
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.854-722A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159321625 | ||||||
| chr4:159321860
|
AATTG | A | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.854-484_854-481del others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr4 | 159321860 | |||||
| chr4:159321991
|
T | C | 4 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.854-356T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159321991 | ||||||
| chr4:159322028
|
CATA | C | 5 | a0001c0001t0002g0149a0001c0001t0005g0024a0001c0001t0008g0062others(2): Show | 5 | HG00558.hp2 HG01943.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.854-311_854-309del others(3): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr4 | 159322028 | |||||
| chr4:159322337
|
T | C | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.854-10T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 9/29 | chr4 | 159322337 | ||||||
| chr4:159322721
|
G | A | 2 | a0001c0001t0009g0058a0001c0001t0009g0059 | 2 | HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.990+238G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 10/29 | chr4 | 159322721 | ||||||
| chr4:159322763
|
A | T | 1 | a0002c0009t0002g0011 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.990+280A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 10/29 | chr4 | 159322763 | ||||||
| chr4:159322791
|
A | G | 3 | a0001c0001t0013g0083a0001c0001t0024g0087a0001c0001t0028g0167 | 3 | HG02559.hp2 HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.990+308A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 10/29 | chr4 | 159322791 | ||||||
| chr4:159322804
|
A | G | 1 | a0001c0002t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.990+321A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 10/29 | chr4 | 159322804 | ||||||
| chr4:159322861
|
A | G | 2 | a0001c0002t0003g0168a0001c0011t0032g0114 | 2 | HG01981.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.990+378A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 10/29 | chr4 | 159322861 | ||||||
| chr4:159322979
|
C | G | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.991-480C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 10/29 | chr4 | 159322979 | ||||||
| chr4:159323060
|
T | C | 76 | a0001c0001t0002g0060a0001c0001t0002g0149a0001c0001t0005g0012others(73): Show | 76 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.991-399T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 10/29 | chr4 | 159323060 | ||||||
| chr4:159323135
|
A | G | 145 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0060others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.991-324A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 10/29 | chr4 | 159323135 | ||||||
| chr4:159323295
|
T | C | 8 | a0001c0001t0004g0193a0001c0002t0001g0157a0001c0002t0003g0172others(5): Show | 8 | HG02717.hp2 HG02723.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.991-164T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 10/29 | chr4 | 159323295 | ||||||
| chr4:159323390
|
C | T | 3 | a0001c0001t0005g0086a0001c0006t0014g0026a0001c0006t0014g0036 | 3 | HG03098.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.991-69C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 10/29 | chr4 | 159323390 | ||||||
| chr4:159323403
|
T | TA | 2 | a0001c0001t0005g0092a0001c0001t0005g0093 | 2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.991-55dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr4 | 159323403 | |||||
| chr4:159323720
|
A | AT | 69 | a0001c0001t0002g0149a0001c0001t0005g0012a0001c0001t0005g0024others(66): Show | 69 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.1149+119dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr4 | 159323720 | |||||
| chr4:159323787
|
C | T | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1149+170C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159323787 | ||||||
| chr4:159323788
|
G | A | 1 | a0001c0003t0004g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1149+171G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159323788 | ||||||
| chr4:159323958
|
G | A | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1149+341G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159323958 | ||||||
| chr4:159324187
|
G | A | 1 | a0001c0001t0021g0028 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1149+570G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159324187 | ||||||
| chr4:159324308
|
G | A | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1149+691G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159324308 | ||||||
| chr4:159324551
|
T | C | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1149+934T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159324551 | ||||||
| chr4:159324939
|
CTAAT | C | 59 | a0001c0001t0002g0149a0001c0001t0005g0012a0001c0001t0005g0051others(56): Show | 59 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1149+1324_1149+132 others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr4 | 159324939 | |||||
| chr4:159325122
|
A | G | 1 | a0001c0002t0030g0137 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1149+1505A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159325122 | ||||||
| chr4:159325446
|
A | C | 1 | a0001c0002t0003g0168 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1149+1829A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159325446 | ||||||
| chr4:159325506
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1149+1889A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159325506 | ||||||
| chr4:159325603
|
G | GT | 99 | a0001c0001t0002g0025a0001c0001t0002g0066a0001c0001t0002g0132others(96): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.1149+1995dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr4 | 159325603 | |||||
| chr4:159325901
|
G | A | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1149+2284G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159325901 | ||||||
| chr4:159325997
|
G | A | 4 | a0001c0001t0005g0024a0001c0002t0001g0027a0001c0002t0001g0038others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.1149+2380G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159325997 | ||||||
| chr4:159326085
|
G | C | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1149+2468G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159326085 | ||||||
| chr4:159326225
|
A | G | 1 | a0001c0001t0031g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1149+2608A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159326225 | ||||||
| chr4:159326225
|
A | T | 37 | a0001c0001t0002g0025a0001c0001t0002g0066a0001c0001t0002g0132others(34): Show | 37 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1149+2608A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159326225 | ||||||
| chr4:159326249
|
G | A | 12 | a0001c0003t0004g0009a0001c0003t0004g0019a0001c0003t0004g0045others(9): Show | 12 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1149+2632G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159326249 | ||||||
| chr4:159326602
|
C | G | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1149+2985C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159326602 | ||||||
| chr4:159326917
|
A | G | 1 | a0001c0002t0003g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1150-2941A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159326917 | ||||||
| chr4:159327332
|
A | G | 1 | a0001c0002t0003g0181 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1150-2526A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159327332 | ||||||
| chr4:159327429
|
C | CGAG | 37 | a0001c0001t0002g0025a0001c0001t0002g0066a0001c0001t0002g0132others(34): Show | 37 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.1150-2427_1150-242 others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr4 | 159327429 | |||||
| chr4:159327526
|
G | A | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1150-2332G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159327526 | ||||||
| chr4:159327654
|
C | CA | 80 | a0001c0001t0004g0193a0001c0001t0008g0067a0001c0001t0009g0035others(77): Show | 80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1150-2190dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr4 | 159327654 | |||||
| chr4:159327783
|
A | C | 1 | a0001c0001t0005g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1150-2075A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159327783 | ||||||
| chr4:159328182
|
A | G | 3 | a0001c0002t0001g0018a0001c0002t0003g0188a0001c0002t0003g0192 | 3 | HG01978.hp1 HG03017.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1150-1676A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159328182 | ||||||
| chr4:159328414
|
A | G | 2 | a0001c0002t0001g0007a0001c0002t0030g0137 | 2 | HG01099.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1150-1444A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159328414 | ||||||
| chr4:159328567
|
T | G | 1 | a0001c0001t0002g0089 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1150-1291T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159328567 | ||||||
| chr4:159328570
|
G | A | 60 | a0001c0001t0002g0149a0001c0001t0005g0012a0001c0001t0005g0024others(57): Show | 60 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.1150-1288G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159328570 | ||||||
| chr4:159328621
|
T | C | 12 | a0001c0003t0004g0009a0001c0003t0004g0019a0001c0003t0004g0045others(9): Show | 12 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1150-1237T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159328621 | ||||||
| chr4:159328787
|
A | G | 1 | a0001c0002t0001g0040 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1150-1071A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159328787 | ||||||
| chr4:159328854
|
T | C | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1150-1004T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159328854 | ||||||
| chr4:159329201
|
A | G | 1 | a0001c0001t0002g0121 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1150-657A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159329201 | ||||||
| chr4:159329543
|
T | C | 100 | a0001c0001t0002g0025a0001c0001t0002g0066a0001c0001t0002g0132others(97): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.1150-315T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159329543 | ||||||
| chr4:159329568
|
A | G | 15 | a0001c0001t0002g0149a0001c0001t0005g0012a0001c0001t0005g0051others(12): Show | 15 | HG00558.hp2 HG01943.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1150-290A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159329568 | ||||||
| chr4:159329595
|
T | C | 3 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0003g0186 | 3 | HG01516.hp2 HG01517.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1150-263T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159329595 | ||||||
| chr4:159329633
|
GTAAAATA others(4): Show |
G | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1150-221_1150-211d others(13): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr4 | 159329633 | |||||
| chr4:159329803
|
G | A | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1150-55G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 11/29 | chr4 | 159329803 | ||||||
| chr4:159330263
|
A | ATGTG | 10 | a0001c0003t0004g0009a0001c0003t0004g0019a0001c0003t0004g0047others(7): Show | 10 | HG01081.hp2 HG02109.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1303-70_1303-69ins others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330263 | |||||
| chr4:159330263
|
A | G | 1 | a0001c0001t0031g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1303-71A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | chr4 | 159330263 | ||||||
| chr4:159330265
|
A | ATATGTGT others(7): Show |
1 | a0001c0001t0031g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1303-68_1303-67ins others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330265 | |||||
| chr4:159330265
|
A | ATG | 68 | a0001c0001t0002g0001a0001c0001t0002g0010a0001c0001t0002g0015others(65): Show | 68 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.1303-39_1303-38dup others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330265 | |||||
| chr4:159330265
|
A | ATGTG | 5 | a0001c0001t0002g0145a0001c0001t0002g0154a0001c0001t0006g0170others(2): Show | 5 | HG00733.hp2 HG01081.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303-41_1303-38dup others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330265 | |||||
| chr4:159330265
|
A | ATGTGTG | 7 | a0001c0001t0002g0121a0001c0001t0005g0086a0001c0001t0009g0035others(4): Show | 7 | HG02280.hp1 HG02970.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1303-43_1303-38dup others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330265 | |||||
| chr4:159330265
|
A | ATGTGTGT others(1): Show |
3 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0165 | 3 | HG01884.hp2 HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1303-45_1303-38dup others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330265 | |||||
| chr4:159330265
|
A | ATGTGTGT others(3): Show |
6 | a0001c0001t0013g0085a0001c0001t0026g0003a0001c0002t0001g0128others(3): Show | 6 | HG02055.hp2 HG02896.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1303-47_1303-38dup others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330265 | |||||
| chr4:159330265
|
A | ATGTGTGT others(5): Show |
7 | a0001c0001t0007g0082a0001c0001t0010g0164a0001c0002t0001g0034others(4): Show | 7 | HG00738.hp1 HG01516.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1303-49_1303-38dup others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330265 | |||||
| chr4:159330265
|
A | ATGTGTGT others(7): Show |
9 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0023g0073others(6): Show | 9 | HG00597.hp1 HG01433.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.1303-51_1303-38dup others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330265 | |||||
| chr4:159330265
|
A | ATGTGTGT others(9): Show |
10 | a0001c0001t0002g0149a0001c0001t0004g0194a0001c0001t0007g0077others(7): Show | 10 | HG00280.hp2 HG00558.hp2 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.1303-53_1303-38dup others(16): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330265 | |||||
| chr4:159330265
|
A | ATGTGTGT others(11): Show |
10 | a0001c0001t0007g0094a0001c0002t0001g0014a0001c0002t0001g0027others(7): Show | 10 | HG00733.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1303-55_1303-38dup others(18): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330265 | |||||
| chr4:159330265
|
A | ATGTGTGT others(13): Show |
13 | a0001c0002t0001g0007a0001c0002t0001g0030a0001c0002t0001g0031others(10): Show | 13 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.1303-57_1303-38dup others(20): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330265 | |||||
| chr4:159330265
|
A | ATGTGTGT others(15): Show |
3 | a0001c0002t0001g0017a0001c0002t0001g0052a0001c0002t0001g0053 | 3 | HG01943.hp1 HG01978.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1303-59_1303-38dup others(22): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330265 | |||||
| chr4:159330265
|
A | G | 12 | a0001c0003t0004g0009a0001c0003t0004g0019a0001c0003t0004g0045others(9): Show | 12 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1303-69A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | chr4 | 159330265 | ||||||
| chr4:159330265
|
ATG | A | 6 | a0001c0001t0002g0122a0001c0001t0009g0058a0001c0001t0009g0146others(3): Show | 6 | HG01981.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1303-39_1303-38del others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330265 | |||||
| chr4:159330265
|
ATGTG | A | 2 | a0001c0001t0002g0057a0001c0001t0009g0059 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1303-41_1303-38del others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330265 | |||||
| chr4:159330295
|
G | GTA | 2 | a0001c0001t0002g0088a0001c0001t0002g0097 | 2 | HG00280.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1303-31_1303-30dup others(2): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330295 | |||||
| chr4:159330295
|
G | GTGTGTGT others(3): Show |
4 | a0001c0001t0008g0070a0001c0001t0033g0113a0001c0001t0034g0115others(1): Show | 4 | HG02922.hp1 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1303-38_1303-37ins others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330295 | |||||
| chr4:159330295
|
G | GTGTGTGT others(5): Show |
4 | a0001c0001t0005g0012a0001c0001t0005g0092a0001c0001t0005g0093others(1): Show | 4 | HG03540.hp1 NA19043.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.1303-38_1303-37ins others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330295 | |||||
| chr4:159330295
|
G | GTGTGTGT others(7): Show |
2 | a0001c0001t0005g0051a0001c0001t0008g0062 | 2 | HG02818.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1303-38_1303-37ins others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330295 | |||||
| chr4:159330295
|
G | GTGTGTGT others(9): Show |
1 | a0001c0001t0008g0067 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1303-38_1303-37ins others(16): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330295 | |||||
| chr4:159330295
|
G | GTGTGTGT others(11): Show |
2 | a0001c0001t0008g0033a0001c0001t0008g0112 | 2 | HG01943.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1303-38_1303-37ins others(18): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330295 | |||||
| chr4:159330295
|
G | GTGTGTGT others(13): Show |
1 | a0001c0001t0008g0041 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1303-38_1303-37ins others(20): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr4 | 159330295 | |||||
| chr4:159330297
|
A | G | 73 | a0001c0001t0005g0086a0001c0001t0006g0170a0001c0001t0009g0035others(70): Show | 73 | HG00280.hp2 HG00597.hp1 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.1303-37A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | chr4 | 159330297 | ||||||
| chr4:159330299
|
A | G | 35 | a0001c0001t0005g0024a0001c0001t0005g0086a0001c0001t0025g0081others(32): Show | 35 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.1303-35A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | chr4 | 159330299 | ||||||
| chr4:159330301
|
A | T | 5 | a0001c0002t0001g0128a0001c0002t0001g0129a0001c0002t0001g0138others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303-33A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 12/29 | chr4 | 159330301 | ||||||
| chr4:159330832
|
G | A | 5 | a0001c0002t0001g0128a0001c0002t0001g0129a0001c0002t0001g0138others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1467+334G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 13/29 | chr4 | 159330832 | ||||||
| chr4:159331149
|
T | C | 12 | a0001c0001t0009g0035a0001c0001t0009g0058a0001c0001t0009g0059others(9): Show | 12 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1468-282T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 13/29 | chr4 | 159331149 | ||||||
| chr4:159331156
|
G | A | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1468-275G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 13/29 | chr4 | 159331156 | ||||||
| chr4:159331243
|
C | A | 10 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(7): Show | 10 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1468-188C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 13/29 | chr4 | 159331243 | ||||||
| chr4:159331265
|
C | G | 2 | a0001c0002t0001g0017a0001c0002t0001g0052 | 2 | HG01943.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1468-166C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 13/29 | chr4 | 159331265 | ||||||
| chr4:159331319
|
T | C | 5 | a0001c0002t0001g0128a0001c0002t0001g0129a0001c0002t0001g0138others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1468-112T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 13/29 | chr4 | 159331319 | ||||||
| chr4:159331389
|
G | A | 12 | a0001c0003t0004g0009a0001c0003t0004g0019a0001c0003t0004g0045others(9): Show | 12 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1468-42G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 13/29 | chr4 | 159331389 | ||||||
| chr4:159331864
|
A | T | 12 | a0001c0003t0004g0009a0001c0003t0004g0019a0001c0003t0004g0045others(9): Show | 12 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1779+31A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 15/29 | chr4 | 159331864 | ||||||
| chr4:159332930
|
T | A | 2 | a0001c0001t0002g0025a0001c0001t0005g0049 | 2 | NA18955.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.2135+233T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159332930 | ||||||
| chr4:159332968
|
TTTTATTT others(5): Show |
T | 2 | a0001c0007t0016g0140a0001c0007t0016g0141 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2135+287_2135+298d others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr4 | 159332968 | |||||
| chr4:159332991
|
T | C | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2135+294T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159332991 | ||||||
| chr4:159333040
|
C | T | 4 | a0001c0001t0002g0071a0001c0001t0011g0021a0001c0001t0011g0022others(1): Show | 4 | HG02258.hp2 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2135+343C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159333040 | ||||||
| chr4:159333042
|
C | T | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2135+345C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159333042 | ||||||
| chr4:159333049
|
G | A | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2135+352G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159333049 | ||||||
| chr4:159333321
|
C | T | 1 | a0001c0002t0012g0156 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2135+624C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159333321 | ||||||
| chr4:159333879
|
C | G | 9 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2135+1182C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159333879 | ||||||
| chr4:159333891
|
T | A | 1 | a0001c0001t0021g0028 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2135+1194T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159333891 | ||||||
| chr4:159334006
|
A | G | 34 | a0001c0001t0002g0025a0001c0001t0004g0193a0001c0001t0005g0049others(31): Show | 34 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.2135+1309A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159334006 | ||||||
| chr4:159334249
|
T | A | 1 | a0001c0001t0002g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2135+1552T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159334249 | ||||||
| chr4:159334368
|
C | T | 3 | a0001c0001t0005g0086a0001c0006t0014g0026a0001c0006t0014g0036 | 3 | HG03098.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2135+1671C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159334368 | ||||||
| chr4:159334423
|
T | A | 5 | a0001c0002t0001g0128a0001c0002t0001g0129a0001c0002t0001g0138others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2135+1726T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159334423 | ||||||
| chr4:159334619
|
T | C | 1 | a0001c0001t0005g0012 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2135+1922T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159334619 | ||||||
| chr4:159334650
|
T | C | 134 | a0001c0001t0002g0025a0001c0001t0002g0149a0001c0001t0004g0193others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.2135+1953T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159334650 | ||||||
| chr4:159334862
|
A | G | 2 | a0001c0007t0016g0140a0001c0007t0016g0141 | 2 | HG01884.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2135+2165A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159334862 | ||||||
| chr4:159334945
|
ATAAT | A | 9 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2135+2252_2135+225 others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr4 | 159334945 | |||||
| chr4:159335090
|
T | G | 9 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2135+2393T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159335090 | ||||||
| chr4:159335126
|
T | C | 1 | a0001c0002t0018g0148 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2135+2429T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159335126 | ||||||
| chr4:159335338
|
G | A | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2135+2641G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159335338 | ||||||
| chr4:159335351
|
A | T | 1 | a0001c0005t0012g0105 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2135+2654A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159335351 | ||||||
| chr4:159335357
|
A | G | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2135+2660A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159335357 | ||||||
| chr4:159335402
|
G | A | 125 | a0001c0001t0002g0025a0001c0001t0002g0149a0001c0001t0004g0193others(122): Show | 125 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.2135+2705G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159335402 | ||||||
| chr4:159335619
|
G | A | 16 | a0001c0001t0004g0194a0001c0001t0013g0083a0001c0001t0013g0084others(13): Show | 16 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2136-2692G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159335619 | ||||||
| chr4:159335644
|
G | A | 12 | a0001c0003t0004g0009a0001c0003t0004g0019a0001c0003t0004g0045others(9): Show | 12 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2136-2667G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159335644 | ||||||
| chr4:159335796
|
A | C | 2 | a0001c0001t0008g0033a0001c0001t0008g0041 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2136-2515A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159335796 | ||||||
| chr4:159335835
|
C | CA | 26 | a0001c0001t0002g0025a0001c0001t0002g0066a0001c0001t0002g0096others(23): Show | 26 | HG00099.hp1 HG00735.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.2136-2452dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr4 | 159335835 | |||||
| chr4:159335835
|
CA | C | 13 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(10): Show | 13 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2136-2452delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr4 | 159335835 | |||||
| chr4:159335882
|
C | G | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2136-2429C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159335882 | ||||||
| chr4:159336157
|
AT | A | 136 | a0001c0001t0002g0025a0001c0001t0002g0044a0001c0001t0002g0130others(133): Show | 136 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.2136-2142delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr4 | 159336157 | |||||
| chr4:159336256
|
G | A | 12 | a0001c0003t0004g0009a0001c0003t0004g0019a0001c0003t0004g0045others(9): Show | 12 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2136-2055G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159336256 | ||||||
| chr4:159336736
|
CA | C | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2136-1565delA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr4 | 159336736 | |||||
| chr4:159336914
|
G | A | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2136-1397G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159336914 | ||||||
| chr4:159337015
|
C | T | 1 | a0001c0001t0002g0010 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2136-1296C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159337015 | ||||||
| chr4:159337087
|
G | C | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2136-1224G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159337087 | ||||||
| chr4:159337230
|
A | G | 1 | a0001c0001t0002g0074 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2136-1081A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159337230 | ||||||
| chr4:159337338
|
A | C | 9 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2136-973A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159337338 | ||||||
| chr4:159337445
|
G | A | 9 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2136-866G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159337445 | ||||||
| chr4:159337475
|
A | G | 3 | a0001c0001t0005g0086a0001c0006t0014g0026a0001c0006t0014g0036 | 3 | HG03098.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2136-836A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159337475 | ||||||
| chr4:159337617
|
T | C | 15 | a0001c0001t0002g0149a0001c0001t0005g0012a0001c0001t0005g0051others(12): Show | 15 | HG00558.hp2 HG01943.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.2136-694T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159337617 | ||||||
| chr4:159337746
|
C | G | 15 | a0001c0001t0002g0149a0001c0001t0005g0012a0001c0001t0005g0051others(12): Show | 15 | HG00558.hp2 HG01943.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.2136-565C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159337746 | ||||||
| chr4:159337782
|
C | T | 37 | a0001c0001t0002g0025a0001c0001t0002g0066a0001c0001t0002g0132others(34): Show | 37 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.2136-529C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159337782 | ||||||
| chr4:159337783
|
A | G | 138 | a0001c0001t0002g0025a0001c0001t0002g0066a0001c0001t0002g0132others(135): Show | 138 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.2136-528A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159337783 | ||||||
| chr4:159337877
|
G | C | 5 | a0001c0001t0009g0058a0001c0001t0009g0059a0001c0001t0009g0146others(2): Show | 5 | HG02622.hp2 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2136-434G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159337877 | ||||||
| chr4:159337889
|
C | CA | 8 | a0001c0001t0002g0044a0001c0001t0005g0024a0001c0001t0020g0120others(5): Show | 8 | HG00735.hp1 HG01069.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.2136-398dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr4 | 159337889 | |||||
| chr4:159337889
|
C | CAAAAAAA others(3): Show |
3 | a0001c0001t0027g0104a0001c0002t0001g0052a0001c0002t0001g0056 | 3 | HG00642.hp2 HG01978.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2136-407_2136-398d others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr4 | 159337889 | |||||
| chr4:159337889
|
C | CAAAAAAA others(4): Show |
10 | a0001c0002t0001g0027a0001c0002t0001g0038a0001c0002t0001g0043others(7): Show | 10 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.2136-408_2136-398d others(13): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr4 | 159337889 | |||||
| chr4:159337889
|
C | CAAAAAAA others(5): Show |
14 | a0001c0002t0001g0006a0001c0002t0001g0014a0001c0002t0001g0030others(11): Show | 14 | HG01074.hp2 HG01109.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2136-409_2136-398d others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr4 | 159337889 | |||||
| chr4:159337889
|
C | CAAAAAAA others(6): Show |
8 | a0001c0002t0001g0017a0001c0002t0001g0031a0001c0002t0001g0034others(5): Show | 8 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.2136-410_2136-398d others(15): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr4 | 159337889 | |||||
| chr4:159337889
|
C | CAAAAAAA others(7): Show |
1 | a0001c0002t0001g0152 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2136-411_2136-398d others(16): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr4 | 159337889 | |||||
| chr4:159337889
|
C | CAAAAAAA others(8): Show |
2 | a0001c0002t0001g0153a0001c0002t0022g0106 | 2 | HG01516.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.2136-412_2136-398d others(17): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr4 | 159337889 | |||||
| chr4:159337889
|
C | CAAAAAAA others(20): Show |
1 | a0001c0002t0001g0139 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2136-398_2136-397i others(29): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr4 | 159337889 | |||||
| chr4:159337889
|
CAAA | C | 37 | a0001c0001t0004g0194a0001c0001t0007g0077a0001c0001t0007g0078others(34): Show | 37 | HG01081.hp2 HG01123.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2136-400_2136-398d others(5): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr4 | 159337889 | |||||
| chr4:159337910
|
A | AAG | 13 | a0001c0001t0002g0149a0001c0001t0005g0012a0001c0001t0005g0051others(10): Show | 13 | HG00558.hp2 HG01943.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.2136-400_2136-399i others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr4 | 159337910 | |||||
| chr4:159338057
|
C | G | 37 | a0001c0001t0004g0194a0001c0001t0007g0077a0001c0001t0007g0078others(34): Show | 37 | HG01081.hp2 HG01123.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.2136-254C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159338057 | ||||||
| chr4:159338100
|
CAAACAAA others(6): Show |
C | 9 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2136-199_2136-187d others(15): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr4 | 159338100 | |||||
| chr4:159338140
|
T | C | 3 | a0001c0001t0005g0086a0001c0006t0014g0026a0001c0006t0014g0036 | 3 | HG03098.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2136-171T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159338140 | ||||||
| chr4:159338254
|
T | G | 2 | a0001c0001t0002g0096a0001c0001t0002g0142 | 2 | HG00735.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2136-57T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159338254 | ||||||
| chr4:159338290
|
C | G | 4 | a0001c0002t0001g0107a0001c0002t0001g0133a0001c0002t0001g0134others(1): Show | 4 | HG00738.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.2136-21C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 17/29 | chr4 | 159338290 | ||||||
| chr4:159338561
|
A | G | 37 | a0001c0001t0002g0025a0001c0001t0002g0066a0001c0001t0002g0132others(34): Show | 37 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.2293+93A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 18/29 | chr4 | 159338561 | ||||||
| chr4:159338603
|
T | C | 37 | a0001c0001t0002g0025a0001c0001t0002g0066a0001c0001t0002g0132others(34): Show | 37 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.2293+135T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 18/29 | chr4 | 159338603 | ||||||
| chr4:159338732
|
G | A | 1 | a0001c0002t0003g0168 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2293+264G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 18/29 | chr4 | 159338732 | ||||||
| chr4:159338853
|
C | T | 3 | a0001c0001t0005g0086a0001c0006t0014g0026a0001c0006t0014g0036 | 3 | HG03098.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2294-261C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 18/29 | chr4 | 159338853 | ||||||
| chr4:159339057
|
G | T | 59 | a0001c0001t0002g0149a0001c0001t0005g0012a0001c0001t0005g0051others(56): Show | 59 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.2294-57G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 18/29 | chr4 | 159339057 | ||||||
| chr4:159339901
|
G | A | 134 | a0001c0001t0002g0025a0001c0001t0002g0149a0001c0001t0004g0193others(131): Show | 134 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.2534+547G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | chr4 | 159339901 | ||||||
| chr4:159340011
|
A | G | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2534+657A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | chr4 | 159340011 | ||||||
| chr4:159340573
|
A | G | 53 | a0001c0001t0002g0025a0001c0001t0002g0066a0001c0001t0002g0132others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2535-991A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | chr4 | 159340573 | ||||||
| chr4:159340667
|
C | CCA | 45 | a0001c0001t0002g0001a0001c0001t0002g0025a0001c0001t0002g0066others(42): Show | 45 | HG00099.hp2 HG00597.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.2535-858_2535-857d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340667 | |||||
| chr4:159340667
|
C | CCACA | 23 | a0001c0001t0002g0044a0001c0001t0002g0099a0001c0001t0002g0124others(20): Show | 23 | HG00558.hp2 HG00597.hp1 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.2535-860_2535-857d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340667 | |||||
| chr4:159340667
|
C | CCACACA | 24 | a0001c0001t0008g0033a0001c0001t0008g0041a0001c0001t0008g0067others(21): Show | 24 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.2535-862_2535-857d others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340667 | |||||
| chr4:159340667
|
C | CCACACAC others(1): Show |
17 | a0001c0001t0029g0002a0001c0002t0001g0007a0001c0002t0001g0032others(14): Show | 17 | HG00280.hp2 HG00733.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.2535-864_2535-857d others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340667 | |||||
| chr4:159340667
|
C | CCACACAC others(3): Show |
3 | a0001c0001t0005g0051a0001c0002t0001g0054a0001c0002t0001g0056 | 3 | HG00642.hp2 HG01993.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2535-866_2535-857d others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340667 | |||||
| chr4:159340667
|
C | CCACACAC others(5): Show |
1 | a0001c0004t0001g0020 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2535-868_2535-857d others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340667 | |||||
| chr4:159340667
|
C | CCACACAC others(7): Show |
1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2535-870_2535-857d others(16): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340667 | |||||
| chr4:159340667
|
CCA | C | 11 | a0001c0001t0002g0088a0001c0001t0002g0090a0001c0001t0002g0091others(8): Show | 11 | HG00099.hp1 HG00280.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.2535-858_2535-857d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340667 | |||||
| chr4:159340667
|
CCACA | C | 5 | a0001c0001t0007g0127a0001c0001t0021g0028a0001c0005t0012g0105others(2): Show | 5 | HG01884.hp1 HG02970.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2535-860_2535-857d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340667 | |||||
| chr4:159340667
|
CCACACA | C | 5 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(2): Show | 5 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2535-862_2535-857d others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340667 | |||||
| chr4:159340667
|
CCACACAC others(9): Show |
C | 1 | a0001c0002t0001g0006 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2535-872_2535-857d others(18): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340667 | |||||
| chr4:159340739
|
C | G | 135 | a0001c0001t0002g0025a0001c0001t0002g0066a0001c0001t0002g0132others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.2535-825C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | chr4 | 159340739 | ||||||
| chr4:159340741
|
AAAAAAC | A | 135 | a0001c0001t0002g0025a0001c0001t0002g0066a0001c0001t0002g0132others(132): Show | 135 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.2535-812_2535-807d others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340741 | |||||
| chr4:159340779
|
C | CCA | 6 | a0001c0001t0005g0049a0001c0002t0001g0037a0001c0002t0003g0179others(3): Show | 6 | HG02809.hp1 HG03139.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.2535-751_2535-750d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340779 | |||||
| chr4:159340779
|
C | CCACA | 7 | a0001c0001t0002g0149a0001c0001t0008g0033a0001c0001t0008g0041others(4): Show | 7 | HG00558.hp2 HG01081.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.2535-753_2535-750d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340779 | |||||
| chr4:159340779
|
C | CCACACA | 13 | a0001c0001t0005g0012a0001c0001t0005g0092a0001c0001t0005g0093others(10): Show | 13 | HG02451.hp2 HG02723.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.2535-755_2535-750d others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340779 | |||||
| chr4:159340779
|
C | CCACACAC others(1): Show |
4 | a0001c0001t0005g0051a0001c0001t0005g0086a0001c0001t0007g0082others(1): Show | 4 | HG01123.hp1 HG01891.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2535-757_2535-750d others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340779 | |||||
| chr4:159340779
|
CCA | C | 50 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(47): Show | 50 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2535-751_2535-750d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340779 | |||||
| chr4:159340779
|
CCACA | C | 16 | a0001c0001t0002g0044a0001c0001t0002g0060a0001c0001t0002g0076others(13): Show | 16 | HG00438.hp2 HG01069.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.2535-753_2535-750d others(6): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340779 | |||||
| chr4:159340779
|
CCACACA | C | 39 | a0001c0001t0021g0028a0001c0002t0001g0006a0001c0002t0001g0007others(36): Show | 39 | HG00280.hp2 HG00597.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.2535-755_2535-750d others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340779 | |||||
| chr4:159340779
|
CCACACAC others(3): Show |
C | 7 | a0001c0001t0009g0035a0001c0001t0010g0155a0001c0001t0010g0162others(4): Show | 7 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2535-759_2535-750d others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340779 | |||||
| chr4:159340779
|
CCACACAC others(5): Show |
C | 5 | a0001c0001t0009g0058a0001c0001t0009g0059a0001c0001t0009g0146others(2): Show | 5 | HG02622.hp2 HG02630.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2535-761_2535-750d others(14): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159340779 | |||||
| chr4:159341145
|
GATAAGAA others(1): Show |
G | 11 | a0001c0001t0009g0035a0001c0001t0009g0058a0001c0001t0009g0059others(8): Show | 11 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2535-405_2535-398d others(10): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | INFO_REALIGN_3_PRIME | chr4 | 159341145 | |||||
| chr4:159341331
|
C | T | 1 | a0001c0002t0003g0178 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2535-233C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | chr4 | 159341331 | ||||||
| chr4:159341447
|
C | A | 1 | a0001c0002t0001g0018 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2535-117C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | chr4 | 159341447 | ||||||
| chr4:159341454
|
T | G | 1 | a0001c0002t0003g0185 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2535-110T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 19/29 | chr4 | 159341454 | ||||||
| chr4:159342066
|
A | T | 3 | a0001c0001t0005g0086a0001c0006t0014g0026a0001c0006t0014g0036 | 3 | HG03098.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2918+119A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | chr4 | 159342066 | ||||||
| chr4:159342233
|
T | G | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2918+286T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | chr4 | 159342233 | ||||||
| chr4:159342254
|
C | T | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2918+307C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | chr4 | 159342254 | ||||||
| chr4:159342329
|
A | G | 1 | a0001c0002t0001g0043 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2918+382A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | chr4 | 159342329 | ||||||
| chr4:159342335
|
G | A | 15 | a0001c0001t0002g0149a0001c0001t0005g0012a0001c0001t0005g0051others(12): Show | 15 | HG00558.hp2 HG01943.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.2918+388G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | chr4 | 159342335 | ||||||
| chr4:159342526
|
C | CTTTTA | 13 | a0001c0001t0009g0035a0001c0002t0001g0006a0001c0002t0001g0017others(10): Show | 13 | HG00733.hp1 HG01109.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.2919-431_2919-427d others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342526 | |||||
| chr4:159342526
|
C | CTTTTATT others(3): Show |
7 | a0001c0001t0002g0025a0001c0001t0005g0049a0001c0002t0001g0013others(4): Show | 7 | HG00099.hp1 HG00735.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.2919-436_2919-427d others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342526 | |||||
| chr4:159342526
|
C | CTTTTATT others(8): Show |
1 | a0001c0001t0010g0162 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2919-441_2919-427d others(17): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342526 | |||||
| chr4:159342526
|
C | CTTTTATT others(33): Show |
1 | a0001c0002t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2919-427_2919-426i others(42): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342526 | |||||
| chr4:159342528
|
TTTATTTT others(18): Show |
T | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2919-426_2919-402d others(27): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342528 | |||||
| chr4:159342533
|
T | TTTATTTT others(18): Show |
4 | a0001c0002t0001g0034a0001c0002t0001g0043a0001c0002t0001g0056others(1): Show | 4 | HG00642.hp2 HG00738.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.2919-427_2919-426i others(27): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342533 | |||||
| chr4:159342533
|
TTTATTTT others(13): Show |
T | 8 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(5): Show | 8 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.2919-426_2919-407d others(22): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342533 | |||||
| chr4:159342538
|
T | TTTATTTT others(13): Show |
1 | a0001c0002t0001g0158 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2919-427_2919-426i others(22): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342538 | |||||
| chr4:159342538
|
T | TTTATTTT others(18): Show |
2 | a0001c0001t0021g0028a0001c0002t0003g0180 | 2 | HG02717.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2919-427_2919-426i others(27): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342538 | |||||
| chr4:159342538
|
TTTATTTT others(8): Show |
T | 2 | a0001c0001t0002g0149a0001c0011t0032g0114 | 2 | HG00558.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.2919-426_2919-412d others(17): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342538 | |||||
| chr4:159342543
|
T | TTTATTTT others(8): Show |
10 | a0001c0001t0010g0155a0001c0001t0010g0164a0001c0001t0010g0165others(7): Show | 10 | HG00639.hp1 HG00639.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.2919-427_2919-426i others(17): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342543 | |||||
| chr4:159342543
|
TTTATTTT others(3): Show |
T | 2 | a0001c0002t0022g0106a0001c0005t0012g0105 | 2 | HG01516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2919-426_2919-417d others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342543 | |||||
| chr4:159342548
|
T | TTTATTTT others(3): Show |
14 | a0001c0001t0027g0104a0001c0002t0001g0027a0001c0002t0001g0038others(11): Show | 14 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.2919-427_2919-426i others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342548 | |||||
| chr4:159342548
|
T | TTTATTTT others(8): Show |
2 | a0001c0002t0001g0048a0001c0002t0003g0166 | 2 | HG03195.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.2919-427_2919-426i others(17): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342548 | |||||
| chr4:159342548
|
TTTATA | T | 5 | a0001c0001t0004g0194a0001c0001t0005g0024a0001c0001t0005g0086others(2): Show | 5 | HG02717.hp1 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2919-426_2919-422d others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342548 | |||||
| chr4:159342553
|
A | ATTATT | 8 | a0001c0001t0002g0001a0001c0001t0002g0088a0001c0001t0002g0110others(5): Show | 8 | HG00280.hp1 HG02040.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.2919-365_2919-361d others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342553 | |||||
| chr4:159342553
|
A | ATTATTTT others(3): Show |
2 | a0001c0001t0002g0074a0001c0001t0002g0097 | 2 | HG01074.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2919-370_2919-361d others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342553 | |||||
| chr4:159342553
|
A | ATTATTTT others(8): Show |
1 | a0001c0001t0009g0059 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2919-375_2919-361d others(17): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342553 | |||||
| chr4:159342553
|
A | ATTATTTT others(33): Show |
1 | a0001c0001t0009g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2919-400_2919-361d others(42): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342553 | |||||
| chr4:159342553
|
A | T | 92 | a0001c0001t0002g0066a0001c0001t0002g0132a0001c0001t0004g0193others(89): Show | 92 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.2919-426A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | chr4 | 159342553 | ||||||
| chr4:159342553
|
ATTATT | A | 17 | a0001c0001t0002g0005a0001c0001t0002g0060a0001c0001t0002g0076others(14): Show | 17 | HG00438.hp2 HG00733.hp2 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.2919-365_2919-361d others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342553 | |||||
| chr4:159342553
|
ATTATTTT others(3): Show |
A | 2 | a0001c0001t0015g0190a0001c0001t0015g0191 | 2 | HG01099.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.2919-370_2919-361d others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342553 | |||||
| chr4:159342553
|
ATTATTTT others(8): Show |
A | 2 | a0001c0001t0002g0015a0001c0001t0006g0170 | 2 | HG01081.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.2919-375_2919-361d others(17): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342553 | |||||
| chr4:159342558
|
T | A | 14 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0025g0081others(11): Show | 14 | HG01934.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2919-421T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | chr4 | 159342558 | ||||||
| chr4:159342558
|
T | TTTATA | 22 | a0001c0001t0002g0132a0001c0001t0006g0163a0001c0002t0001g0004others(19): Show | 22 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.2919-417_2919-416i others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342558 | |||||
| chr4:159342558
|
T | TTTATTTT others(3): Show |
6 | a0001c0001t0008g0033a0001c0001t0008g0112a0001c0001t0029g0002others(3): Show | 6 | HG01943.hp2 HG02486.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2919-412_2919-411i others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342558 | |||||
| chr4:159342563
|
T | A | 10 | a0001c0001t0002g0066a0001c0001t0004g0193a0001c0001t0004g0194others(7): Show | 10 | HG02717.hp1 HG02809.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.2919-416T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | chr4 | 159342563 | ||||||
| chr4:159342563
|
T | TTTATA | 7 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0005g0092others(4): Show | 7 | HG01981.hp1 HG02165.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2919-412_2919-411i others(7): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342563 | |||||
| chr4:159342568
|
T | A | 4 | a0001c0001t0008g0041a0001c0001t0008g0070a0001c0002t0022g0106others(1): Show | 4 | HG01516.hp1 HG02145.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2919-411T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | chr4 | 159342568 | ||||||
| chr4:159342573
|
T | A | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2919-406T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | chr4 | 159342573 | ||||||
| chr4:159342578
|
T | A | 9 | a0001c0001t0002g0149a0001c0001t0007g0077a0001c0001t0007g0078others(6): Show | 9 | HG00558.hp2 HG01123.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.2919-401T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | chr4 | 159342578 | ||||||
| chr4:159342583
|
T | A | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2919-396T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | chr4 | 159342583 | ||||||
| chr4:159342593
|
T | TTTATCTT others(38): Show |
1 | a0001c0006t0014g0026 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2919-382_2919-381i others(47): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342593 | |||||
| chr4:159342593
|
T | TTTATTTT others(63): Show |
1 | a0001c0006t0014g0036 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2919-362_2919-361i others(72): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr4 | 159342593 | |||||
| chr4:159342722
|
C | T | 77 | a0001c0001t0002g0025a0001c0001t0002g0066a0001c0001t0002g0132others(74): Show | 77 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.2919-257C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | chr4 | 159342722 | ||||||
| chr4:159342768
|
C | G | 53 | a0001c0001t0002g0025a0001c0001t0002g0066a0001c0001t0002g0132others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2919-211C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | chr4 | 159342768 | ||||||
| chr4:159342874
|
T | A | 43 | a0001c0001t0027g0104a0001c0002t0001g0006a0001c0002t0001g0007others(40): Show | 43 | HG00280.hp2 HG00597.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.2919-105T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | chr4 | 159342874 | ||||||
| chr4:159342928
|
G | T | 9 | a0001c0002t0001g0107a0001c0002t0001g0108a0001c0002t0001g0111others(6): Show | 9 | HG00099.hp2 HG00735.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.2919-51G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 20/29 | chr4 | 159342928 | ||||||
| chr4:159343469
|
A | G | 1 | a0001c0001t0007g0082 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3254+65A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 22/29 | chr4 | 159343469 | ||||||
| chr4:159343475
|
T | C | 2 | a0001c0002t0001g0128a0001c0002t0001g0129 | 2 | HG02280.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.3254+71T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 22/29 | chr4 | 159343475 | ||||||
| chr4:159343510
|
G | A | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3254+106G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 22/29 | chr4 | 159343510 | ||||||
| chr4:159343565
|
A | G | 12 | a0001c0001t0009g0035a0001c0001t0009g0058a0001c0001t0009g0059others(9): Show | 12 | HG01884.hp2 HG02257.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.3254+161A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 22/29 | chr4 | 159343565 | ||||||
| chr4:159343925
|
T | C | 3 | a0001c0001t0005g0086a0001c0006t0014g0026a0001c0006t0014g0036 | 3 | HG03098.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3255-111T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 22/29 | chr4 | 159343925 | ||||||
| chr4:159344463
|
A | G | 2 | a0001c0001t0002g0060a0001c0001t0006g0175 | 2 | HG00438.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.3278+404A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 23/29 | chr4 | 159344463 | ||||||
| chr4:159345504
|
G | T | 71 | a0001c0001t0002g0025a0001c0001t0004g0193a0001c0001t0004g0194others(68): Show | 71 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.3502+175G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 24/29 | chr4 | 159345504 | ||||||
| chr4:159345728
|
T | A | 3 | a0001c0001t0005g0086a0001c0006t0014g0026a0001c0006t0014g0036 | 3 | HG03098.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3502+399T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 24/29 | chr4 | 159345728 | ||||||
| chr4:159345729
|
T | A | 3 | a0001c0001t0005g0086a0001c0006t0014g0026a0001c0006t0014g0036 | 3 | HG03098.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3502+400T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 24/29 | chr4 | 159345729 | ||||||
| chr4:159345730
|
T | A | 3 | a0001c0001t0005g0086a0001c0006t0014g0026a0001c0006t0014g0036 | 3 | HG03098.hp1 HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3502+401T>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 24/29 | chr4 | 159345730 | ||||||
| chr4:159345839
|
A | G | 12 | a0001c0003t0004g0009a0001c0003t0004g0019a0001c0003t0004g0045others(9): Show | 12 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.3502+510A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 24/29 | chr4 | 159345839 | ||||||
| chr4:159345851
|
G | GT | 5 | a0001c0001t0002g0130a0001c0005t0005g0016a0001c0006t0014g0026others(2): Show | 5 | HG02257.hp1 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.3502+535dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr4 | 159345851 | |||||
| chr4:159345864
|
T | C | 1 | a0001c0002t0001g0042 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3502+535T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 24/29 | chr4 | 159345864 | ||||||
| chr4:159345952
|
C | T | 3 | a0001c0002t0001g0027a0001c0002t0001g0038a0001c0002t0001g0039 | 3 | HG01069.hp2 HG01071.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.3502+623C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 24/29 | chr4 | 159345952 | ||||||
| chr4:159346063
|
G | A | 1 | a0001c0001t0021g0028 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3503-726G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 24/29 | chr4 | 159346063 | ||||||
| chr4:159346152
|
G | A | 3 | a0001c0002t0001g0031a0001c0002t0001g0050a0001c0002t0001g0143 | 3 | HG00639.hp1 HG01109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3503-637G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 24/29 | chr4 | 159346152 | ||||||
| chr4:159346182
|
T | C | 42 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0014others(39): Show | 42 | HG00280.hp2 HG00597.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.3503-607T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 24/29 | chr4 | 159346182 | ||||||
| chr4:159346585
|
T | G | 3 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0003g0186 | 3 | HG01516.hp2 HG01517.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3503-204T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 24/29 | chr4 | 159346585 | ||||||
| chr4:159346784
|
A | G | 9 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.3503-5A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 24/29 | chr4 | 159346784 | ||||||
| chr4:159347208
|
A | G | 2 | a0001c0001t0002g0044a0001c0001t0002g0099 | 2 | HG01069.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3712+210A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159347208 | ||||||
| chr4:159347223
|
G | C | 11 | a0001c0001t0009g0035a0001c0001t0009g0058a0001c0001t0009g0059others(8): Show | 11 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.3712+225G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159347223 | ||||||
| chr4:159347348
|
A | G | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3712+350A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159347348 | ||||||
| chr4:159347477
|
A | G | 42 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0014others(39): Show | 42 | HG00280.hp2 HG00597.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.3712+479A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159347477 | ||||||
| chr4:159347645
|
G | A | 1 | a0001c0001t0021g0028 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3712+647G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159347645 | ||||||
| chr4:159347657
|
G | A | 53 | a0001c0001t0002g0025a0001c0001t0002g0066a0001c0001t0002g0132others(50): Show | 53 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.3712+659G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159347657 | ||||||
| chr4:159347700
|
C | T | 1 | a0001c0001t0005g0051 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3712+702C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159347700 | ||||||
| chr4:159347978
|
C | G | 4 | a0001c0001t0005g0086a0001c0006t0014g0026a0001c0006t0014g0036others(1): Show | 4 | HG02257.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3712+980C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159347978 | ||||||
| chr4:159347992
|
G | A | 59 | a0001c0001t0002g0149a0001c0001t0005g0012a0001c0001t0005g0051others(56): Show | 59 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.3712+994G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159347992 | ||||||
| chr4:159348024
|
C | G | 11 | a0001c0001t0009g0035a0001c0001t0009g0058a0001c0001t0009g0059others(8): Show | 11 | HG01884.hp2 HG02615.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.3712+1026C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159348024 | ||||||
| chr4:159348218
|
C | CGATA | 6 | a0001c0001t0031g0116a0001c0003t0004g0019a0001c0003t0004g0045others(3): Show | 6 | HG01081.hp2 HG02257.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.3712+1244_3712+124 others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr4 | 159348218 | |||||
| chr4:159348218
|
C | CGATAGAT others(9): Show |
1 | a0001c0001t0013g0083 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3712+1232_3712+124 others(20): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr4 | 159348218 | |||||
| chr4:159348218
|
C | CGATAGAT others(13): Show |
1 | a0001c0001t0013g0084 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3712+1228_3712+124 others(24): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr4 | 159348218 | |||||
| chr4:159348218
|
CGATA | C | 6 | a0001c0001t0009g0035a0001c0001t0009g0058a0001c0001t0009g0146others(3): Show | 6 | HG02074.hp1 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3712+1244_3712+124 others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr4 | 159348218 | |||||
| chr4:159348238
|
AGATAGAT others(1): Show |
A | 6 | a0001c0001t0002g0015a0001c0001t0009g0059a0001c0001t0010g0155others(3): Show | 6 | HG01433.hp2 HG01884.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3712+1244_3712+125 others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr4 | 159348238 | |||||
| chr4:159348238
|
AGATAGAT others(9): Show |
A | 5 | a0001c0002t0001g0128a0001c0002t0001g0129a0001c0002t0001g0138others(2): Show | 5 | HG02055.hp2 HG02280.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.3712+1244_3712+125 others(20): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr4 | 159348238 | |||||
| chr4:159348242
|
A | AGATAGAT others(17): Show |
1 | a0001c0001t0013g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3712+1247_3712+124 others(28): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr4 | 159348242 | |||||
| chr4:159348242
|
A | AGATAGAT others(13): Show |
1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3712+1247_3712+124 others(24): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr4 | 159348242 | |||||
| chr4:159348242
|
A | AGATAGAT others(5): Show |
2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3712+1247_3712+124 others(16): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr4 | 159348242 | |||||
| chr4:159348242
|
A | AGATG | 8 | a0001c0001t0002g0066a0001c0001t0002g0132a0001c0001t0005g0086others(5): Show | 8 | HG00735.hp1 HG01981.hp1 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.3712+1284_3712+128 others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr4 | 159348242 | |||||
| chr4:159348242
|
A | AGATGGAT others(1): Show |
19 | a0001c0001t0004g0193a0001c0002t0001g0018a0001c0002t0001g0107others(16): Show | 19 | HG00099.hp2 HG00738.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.3712+1280_3712+128 others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr4 | 159348242 | |||||
| chr4:159348242
|
A | G | 1 | a0001c0001t0025g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3712+1244A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159348242 | ||||||
| chr4:159348242
|
AGATG | A | 47 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0010others(44): Show | 47 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.3712+1284_3712+128 others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr4 | 159348242 | |||||
| chr4:159348242
|
AGATGGAT others(1): Show |
A | 2 | a0001c0001t0005g0024a0001c0001t0029g0002 | 2 | HG02717.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3712+1280_3712+128 others(12): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr4 | 159348242 | |||||
| chr4:159348242
|
AGATGGAT others(5): Show |
A | 51 | a0001c0001t0002g0149a0001c0001t0005g0012a0001c0001t0005g0051others(48): Show | 51 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.3712+1276_3712+128 others(16): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr4 | 159348242 | |||||
| chr4:159348246
|
G | A | 24 | a0001c0001t0002g0145a0001c0001t0006g0184a0001c0001t0007g0078others(21): Show | 24 | HG00733.hp2 HG01081.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.3712+1248G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159348246 | ||||||
| chr4:159348250
|
G | A | 2 | a0001c0001t0021g0028a0001c0005t0012g0105 | 2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3712+1252G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159348250 | ||||||
| chr4:159348254
|
G | A | 1 | a0001c0001t0029g0002 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3712+1256G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159348254 | ||||||
| chr4:159348282
|
G | GGATGGAT others(5): Show |
1 | a0001c0002t0001g0157 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3712+1287_3712+128 others(16): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr4 | 159348282 | |||||
| chr4:159348511
|
A | G | 4 | a0001c0001t0005g0086a0001c0006t0014g0026a0001c0006t0014g0036others(1): Show | 4 | HG02257.hp1 HG03098.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3712+1513A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159348511 | ||||||
| chr4:159348568
|
G | A | 4 | a0001c0002t0001g0027a0001c0002t0001g0038a0001c0002t0001g0039others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.3713-1569G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159348568 | ||||||
| chr4:159348577
|
T | C | 1 | a0001c0002t0001g0018 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3713-1560T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159348577 | ||||||
| chr4:159348616
|
C | T | 2 | a0001c0006t0014g0026a0001c0006t0014g0036 | 2 | HG03130.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3713-1521C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159348616 | ||||||
| chr4:159348628
|
A | G | 1 | a0001c0001t0021g0028 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3713-1509A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159348628 | ||||||
| chr4:159348872
|
A | G | 1 | a0001c0001t0021g0028 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3713-1265A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159348872 | ||||||
| chr4:159348926
|
A | G | 3 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085 | 3 | HG02559.hp2 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3713-1211A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159348926 | ||||||
| chr4:159349032
|
A | G | 15 | a0001c0001t0002g0149a0001c0001t0005g0012a0001c0001t0005g0051others(12): Show | 15 | HG00558.hp2 HG01943.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.3713-1105A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159349032 | ||||||
| chr4:159349080
|
T | C | 63 | a0001c0001t0002g0149a0001c0001t0005g0012a0001c0001t0005g0024others(60): Show | 63 | HG00280.hp2 HG00558.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.3713-1057T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159349080 | ||||||
| chr4:159349224
|
G | A | 1 | a0001c0001t0008g0062 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.3713-913G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159349224 | ||||||
| chr4:159349494
|
GCTGGCT | G | 43 | a0001c0001t0027g0104a0001c0002t0001g0006a0001c0002t0001g0007others(40): Show | 43 | HG00280.hp2 HG00597.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.3713-641_3713-636d others(8): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr4 | 159349494 | |||||
| chr4:159349515
|
G | A | 1 | a0001c0001t0009g0035 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3713-622G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159349515 | ||||||
| chr4:159349530
|
G | A | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3713-607G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159349530 | ||||||
| chr4:159349572
|
C | T | 2 | a0001c0001t0008g0033a0001c0001t0008g0041 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3713-565C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159349572 | ||||||
| chr4:159349587
|
T | C | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3713-550T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159349587 | ||||||
| chr4:159349623
|
G | A | 1 | a0001c0002t0003g0182 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3713-514G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159349623 | ||||||
| chr4:159349830
|
C | T | 3 | a0001c0001t0005g0024a0001c0002t0012g0151a0001c0002t0012g0156 | 3 | HG02717.hp1 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3713-307C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159349830 | ||||||
| chr4:159349846
|
A | G | 3 | a0001c0001t0005g0024a0001c0002t0012g0151a0001c0002t0012g0156 | 3 | HG02717.hp1 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3713-291A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159349846 | ||||||
| chr4:159349865
|
C | T | 33 | a0001c0001t0002g0025a0001c0001t0004g0193a0001c0001t0005g0049others(30): Show | 33 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.3713-272C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | chr4 | 159349865 | ||||||
| chr4:159350116
|
G | GT | 15 | a0001c0001t0002g0149a0001c0001t0005g0012a0001c0001t0005g0051others(12): Show | 15 | HG00558.hp2 HG01943.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.3713-10dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr4 | 159350116 | |||||
| chr4:159350116
|
GT | G | 42 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0014others(39): Show | 42 | HG00280.hp2 HG00597.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.3713-10delT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr4 | 159350116 | |||||
| chr4:159350340
|
G | A | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3865+51G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 26/29 | chr4 | 159350340 | ||||||
| chr4:159350490
|
A | G | 12 | a0001c0003t0004g0009a0001c0003t0004g0019a0001c0003t0004g0045others(9): Show | 12 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.3865+201A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 26/29 | chr4 | 159350490 | ||||||
| chr4:159351302
|
C | CT | 25 | a0001c0001t0009g0035a0001c0001t0010g0155a0001c0001t0010g0162others(22): Show | 25 | HG01081.hp2 HG01884.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.3865+1025dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr4 | 159351302 | |||||
| chr4:159351401
|
A | G | 4 | a0001c0001t0002g0044a0001c0001t0002g0099a0001c0004t0001g0020others(1): Show | 4 | HG00280.hp2 HG01069.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.3865+1112A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 26/29 | chr4 | 159351401 | ||||||
| chr4:159351665
|
G | A | 5 | a0001c0001t0010g0155a0001c0001t0010g0162a0001c0001t0010g0164others(2): Show | 5 | HG01884.hp2 HG02615.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.3866-1020G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 26/29 | chr4 | 159351665 | ||||||
| chr4:159351680
|
C | T | 5 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085others(2): Show | 5 | HG02559.hp2 HG02647.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3866-1005C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 26/29 | chr4 | 159351680 | ||||||
| chr4:159351778
|
T | C | 3 | a0001c0001t0013g0083a0001c0001t0013g0084a0001c0001t0013g0085 | 3 | HG02559.hp2 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3866-907T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 26/29 | chr4 | 159351778 | ||||||
| chr4:159351789
|
C | CA | 13 | a0001c0001t0002g0044a0001c0001t0002g0060a0001c0001t0002g0076others(10): Show | 13 | HG00438.hp2 HG01069.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.3866-884dupA | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr4 | 159351789 | |||||
| chr4:159351951
|
A | T | 2 | a0001c0001t0021g0028a0001c0002t0003g0166 | 2 | HG02970.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3866-734A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 26/29 | chr4 | 159351951 | ||||||
| chr4:159352111
|
C | T | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3866-574C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 26/29 | chr4 | 159352111 | ||||||
| chr4:159352523
|
A | G | 1 | a0001c0001t0004g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3866-162A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 26/29 | chr4 | 159352523 | ||||||
| chr4:159353028
|
G | C | 128 | a0001c0001t0002g0066a0001c0001t0002g0132a0001c0001t0004g0193others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.4091+118G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 27/29 | chr4 | 159353028 | ||||||
| chr4:159353243
|
A | AT | 126 | a0001c0001t0002g0066a0001c0001t0002g0132a0001c0001t0004g0194others(123): Show | 126 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.4092-231dupT | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr4 | 159353243 | |||||
| chr4:159353265
|
G | A | 12 | a0001c0001t0005g0024a0001c0001t0008g0033a0001c0001t0008g0041others(9): Show | 12 | HG01943.hp2 HG02145.hp2 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.4092-222G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 27/29 | chr4 | 159353265 | ||||||
| chr4:159353323
|
A | G | 1 | a0001c0002t0001g0152 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.4092-164A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 27/29 | chr4 | 159353323 | ||||||
| chr4:159354481
|
T | C | 74 | a0001c0001t0002g0066a0001c0001t0002g0132a0001c0001t0006g0163others(71): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.4651+435T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 28/29 | chr4 | 159354481 | ||||||
| chr4:159354488
|
A | C | 1 | a0001c0001t0005g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4651+442A>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 28/29 | chr4 | 159354488 | ||||||
| chr4:159354580
|
C | T | 4 | a0001c0001t0008g0070a0001c0001t0029g0002a0001c0001t0033g0113others(1): Show | 4 | HG02922.hp1 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.4651+534C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 28/29 | chr4 | 159354580 | ||||||
| chr4:159354615
|
CCT | C | 10 | a0001c0001t0008g0033a0001c0001t0008g0041a0001c0001t0008g0062others(7): Show | 10 | HG01943.hp2 HG02145.hp2 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.4651+570_4651+571d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 28/29 | chr4 | 159354615 | ||||||
| chr4:159354764
|
C | T | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4651+718C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 28/29 | chr4 | 159354764 | ||||||
| chr4:159354899
|
G | A | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4651+853G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 28/29 | chr4 | 159354899 | ||||||
| chr4:159355172
|
A | G | 42 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0014others(39): Show | 42 | HG00280.hp2 HG00597.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.4652-681A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 28/29 | chr4 | 159355172 | ||||||
| chr4:159355234
|
A | G | 9 | a0001c0001t0008g0033a0001c0001t0008g0041a0001c0001t0008g0062others(6): Show | 9 | HG01943.hp2 HG02145.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.4652-619A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 28/29 | chr4 | 159355234 | ||||||
| chr4:159355241
|
G | T | 1 | a0001c0001t0002g0074 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4652-612G>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 28/29 | chr4 | 159355241 | ||||||
| chr4:159355302
|
T | C | 1 | a0001c0002t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4652-551T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 28/29 | chr4 | 159355302 | ||||||
| chr4:159355306
|
C | T | 1 | a0001c0002t0003g0136 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4652-547C>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 28/29 | chr4 | 159355306 | ||||||
| chr4:159355307
|
G | A | 9 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.4652-546G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 28/29 | chr4 | 159355307 | ||||||
| chr4:159355440
|
A | G | 5 | a0001c0001t0002g0025a0001c0001t0002g0125a0001c0001t0002g0131others(2): Show | 5 | HG00558.hp1 HG00597.hp2 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.4652-413A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 28/29 | chr4 | 159355440 | ||||||
| chr4:159355533
|
G | A | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4652-320G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 28/29 | chr4 | 159355533 | ||||||
| chr4:159355534
|
G | C | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4652-319G>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 28/29 | chr4 | 159355534 | ||||||
| chr4:159355535
|
T | C | 1 | a0001c0001t0026g0003 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4652-318T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 28/29 | chr4 | 159355535 | ||||||
| chr4:159355619
|
A | G | 2 | a0001c0001t0024g0087a0001c0001t0028g0167 | 2 | HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.4652-234A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 28/29 | chr4 | 159355619 | ||||||
| chr4:159356248
|
A | G | 7 | a0001c0002t0001g0157a0001c0002t0003g0172a0001c0002t0003g0178others(4): Show | 7 | HG02717.hp2 HG02723.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.4957+90A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | chr4 | 159356248 | ||||||
| chr4:159356330
|
T | C | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4957+172T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | chr4 | 159356330 | ||||||
| chr4:159356334
|
T | TTG | 9 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(6): Show | 9 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.4957+192_4957+193d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr4 | 159356334 | |||||
| chr4:159356335
|
T | G | 1 | a0001c0011t0032g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4957+177T>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | chr4 | 159356335 | ||||||
| chr4:159356505
|
C | G | 130 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0005g0012others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.4957+347C>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | chr4 | 159356505 | ||||||
| chr4:159356573
|
G | A | 2 | a0001c0002t0003g0172a0001c0002t0003g0179 | 2 | HG02897.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4957+415G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | chr4 | 159356573 | ||||||
| chr4:159356784
|
C | A | 4 | a0001c0002t0001g0013a0001c0002t0001g0102a0001c0002t0003g0136others(1): Show | 4 | HG01071.hp1 HG01123.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.4957+626C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | chr4 | 159356784 | ||||||
| chr4:159356891
|
ACT | A | 4 | a0001c0001t0005g0012a0001c0001t0005g0051a0001c0001t0005g0092others(1): Show | 4 | HG02818.hp2 NA19043.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.4957+736_4957+737d others(4): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr4 | 159356891 | |||||
| chr4:159356926
|
T | C | 128 | a0001c0001t0002g0066a0001c0001t0002g0132a0001c0001t0004g0193others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.4957+768T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | chr4 | 159356926 | ||||||
| chr4:159357158
|
G | A | 7 | a0001c0001t0007g0077a0001c0001t0007g0078a0001c0001t0007g0082others(4): Show | 7 | HG01123.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.4958-956G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | chr4 | 159357158 | ||||||
| chr4:159357222
|
G | A | 1 | a0001c0002t0022g0106 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4958-892G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | chr4 | 159357222 | ||||||
| chr4:159357239
|
T | C | 1 | a0001c0001t0021g0028 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4958-875T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | chr4 | 159357239 | ||||||
| chr4:159357372
|
G | A | 1 | a0001c0001t0005g0024 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4958-742G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | chr4 | 159357372 | ||||||
| chr4:159357433
|
G | A | 41 | a0001c0002t0001g0006a0001c0002t0001g0007a0001c0002t0001g0014others(38): Show | 41 | HG00280.hp2 HG00597.hp1 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.4958-681G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | chr4 | 159357433 | ||||||
| chr4:159357454
|
A | G | 35 | a0001c0001t0002g0066a0001c0001t0002g0132a0001c0001t0006g0163others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.4958-660A>G | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | chr4 | 159357454 | ||||||
| chr4:159357489
|
A | T | 128 | a0001c0001t0002g0066a0001c0001t0002g0132a0001c0001t0004g0193others(125): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.4958-625A>T | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | chr4 | 159357489 | ||||||
| chr4:159357821
|
C | A | 1 | a0001c0002t0003g0169 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.4958-293C>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | chr4 | 159357821 | ||||||
| chr4:159357826
|
G | A | 1 | a0001c0001t0027g0104 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4958-288G>A | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | chr4 | 159357826 | ||||||
| chr4:159357964
|
T | C | 1 | a0001c0002t0003g0160 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4958-150T>C | RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 29/29 | chr4 | 159357964 |