| geneid | 55103 |
|---|---|
| ensemblid | ENSG00000116191.19 |
| hgncid | 30279 |
| symbol | RALGPS2 |
| name | Ral GEF with PH domain and SH3 binding motif 2 |
| refseq_nuc | NM_152663.5 |
| refseq_prot | NP_689876.2 |
| ensembl_nuc | ENST00000367635.8 |
| ensembl_prot | ENSP00000356607.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 178725244 |
| end | 178921840 |
| strand | + |
| ver | v1.2 |
| region | chr1:178725244-178921840 |
| region5000 | chr1:178720244-178926840 |
| regionname0 | RALGPS2_chr1_178725244_178921840 |
| regionname5000 | RALGPS2_chr1_178720244_178926840 |
| 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 | 583 | 305 | 85 | 56 | 134 | 6 | 22 | 106 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0002 | 0/0 | 583 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| 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 | 1/1 | 1752 | 257 | 72 | 45 | 112 | 4 | 22 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| c0002 | 0/0 | 1752 | 45 | 11 | 10 | 22 | 2 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| c0003 | 0/0 | 1752 | 2 | 1 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| c0004 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| c0005 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 5744 | 133 | 21 | 25 | 70 | 3 | 14 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0002 | 0/0 | 5744 | 48 | 5 | 9 | 30 | 0 | 4 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0003 | 0/0 | 5740 | 22 | 0 | 1 | 21 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0004 | 0/0 | 5740 | 11 | 7 | 4 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0005 | 0/0 | 5744 | 8 | 1 | 5 | 0 | 2 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0006 | 0/0 | 5744 | 8 | 8 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0007 | 0/0 | 5741 | 7 | 6 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0008 | 0/0 | 5744 | 6 | 6 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0009 | 0/0 | 5744 | 6 | 6 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0010 | 0/0 | 5741 | 6 | 6 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0011 | 0/0 | 5750 | 4 | 0 | 1 | 3 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0012 | 0/0 | 5744 | 4 | 1 | 1 | 0 | 0 | 2 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0013 | 0/0 | 5744 | 4 | 0 | 4 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0014 | 0/0 | 5744 | 3 | 0 | 0 | 3 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0015 | 0/0 | 5744 | 2 | 0 | 0 | 0 | 1 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0016 | 0/0 | 5744 | 2 | 1 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0017 | 0/0 | 5744 | 2 | 1 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0018 | 0/0 | 5744 | 2 | 0 | 2 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0019 | 0/0 | 5744 | 2 | 2 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0020 | 0/0 | 5744 | 2 | 2 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0021 | 0/0 | 5744 | 2 | 2 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0022 | 1/0 | 5741 | 2 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0023 | 0/0 | 5741 | 2 | 2 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0024 | 0/0 | 5740 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0025 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0026 | 0/1 | 5744 | 1 | 0 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0027 | 0/0 | 5744 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0028 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0029 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0030 | 0/0 | 5744 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0031 | 0/0 | 5744 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0032 | 0/0 | 5744 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0033 | 0/0 | 5744 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0034 | 0/0 | 5744 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0035 | 0/0 | 5744 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0036 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0037 | 0/0 | 5744 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0038 | 0/0 | 5744 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0039 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0040 | 0/0 | 5744 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| t0041 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0061 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0271 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| 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 | 1/1 | 1752 | 257 | 72 | 45 | 112 | 4 | 22 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0002 | 0/0 | 1752 | 45 | 11 | 10 | 22 | 2 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0003 | 0/0 | 1752 | 2 | 1 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0004 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0002c0005 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7495 | 133 | 21 | 25 | 70 | 3 | 14 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0002 | 0/0 | 7495 | 48 | 5 | 9 | 30 | 0 | 4 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0006 | 0/0 | 7495 | 8 | 8 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0007 | 0/0 | 7492 | 7 | 6 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0008 | 0/0 | 7495 | 6 | 6 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0009 | 0/0 | 7495 | 6 | 6 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0010 | 0/0 | 7492 | 6 | 6 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0011 | 0/0 | 7501 | 4 | 0 | 1 | 3 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0012 | 0/0 | 7495 | 4 | 1 | 1 | 0 | 0 | 2 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0013 | 0/0 | 7495 | 4 | 0 | 4 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0014 | 0/0 | 7495 | 3 | 0 | 0 | 3 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0015 | 0/0 | 7495 | 2 | 0 | 0 | 0 | 1 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0016 | 0/0 | 7495 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0018 | 0/0 | 7495 | 2 | 0 | 2 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0019 | 0/0 | 7495 | 2 | 2 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0020 | 0/0 | 7495 | 2 | 2 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0021 | 0/0 | 7495 | 2 | 2 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0022 | 1/0 | 7492 | 2 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0026 | 0/1 | 7495 | 1 | 0 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0027 | 0/0 | 7495 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0028 | 0/0 | 7495 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0029 | 0/0 | 7495 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0030 | 0/0 | 7495 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0031 | 0/0 | 7495 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0032 | 0/0 | 7495 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0033 | 0/0 | 7495 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0034 | 0/0 | 7495 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0035 | 0/0 | 7495 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0036 | 0/0 | 7495 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0037 | 0/0 | 7495 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0038 | 0/0 | 7495 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0040 | 0/0 | 7495 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0001t0041 | 0/0 | 7492 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0002t0003 | 0/0 | 7491 | 22 | 0 | 1 | 21 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0002t0004 | 0/0 | 7491 | 10 | 6 | 4 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0002t0005 | 0/0 | 7495 | 8 | 1 | 5 | 0 | 2 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0002t0016 | 0/0 | 7495 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0002t0023 | 0/0 | 7492 | 2 | 2 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0002t0024 | 0/0 | 7491 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0002t0025 | 0/0 | 7495 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0003t0017 | 0/0 | 7495 | 2 | 1 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0001c0004t0004 | 0/0 | 7491 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| a0002c0005t0039 | 0/0 | 7495 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | copy fasta | chr1 | 178720244 | 178926840 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0006g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0006g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0007g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0007g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0008g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0008g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0008g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0008g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0008g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0009g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0009g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0009g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0009g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0010g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0010g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0010g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0010g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0010g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0010g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0011g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0011g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0011g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0011g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0012g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0012g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0012g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0012g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0013g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0013g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0013g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0013g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0014g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0014g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0014g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0015g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0015g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0016g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0018g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0018g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0019g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0019g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0020g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0020g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0021g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0021g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0022g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0022g0061 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0026g0271 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0027g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0028g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0029g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0030g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0031g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0032g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0033g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0034g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0035g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0036g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0037g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0038g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0040g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0041g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0005g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0005g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0005g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0005g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0005g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0005g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0005g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0016g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0023g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0023g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0024g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0025g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0003t0017g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0003t0017g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0004t0004g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0002c0005t0039g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0005 | g0007 | EUR | GBR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | FIN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00280 | hp2 | a0001 | c0001 | t0015 | g0108 | EUR | FIN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00423 | hp1 | a0001 | c0002 | t0016 | g0030 | EAS | CHS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00544 | hp1 | a0001 | c0002 | t0003 | g0028 | EAS | CHS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00544 | hp2 | a0001 | c0001 | t0014 | g0275 | EAS | CHS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0026 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00733 | hp1 | a0001 | c0002 | t0005 | g0011 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00738 | hp1 | a0001 | c0002 | t0005 | g0010 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00738 | hp2 | a0001 | c0001 | t0012 | g0041 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01069 | hp2 | a0001 | c0002 | t0005 | g0036 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01070 | hp2 | a0001 | c0002 | t0004 | g0127 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01071 | hp1 | a0001 | c0002 | t0005 | g0037 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01071 | hp2 | a0001 | c0002 | t0004 | g0128 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0296 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01074 | hp2 | a0001 | c0002 | t0004 | g0120 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01099 | hp1 | a0001 | c0003 | t0017 | g0151 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01106 | hp1 | a0001 | c0001 | t0013 | g0208 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01168 | hp1 | a0001 | c0001 | t0018 | g0080 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01169 | hp1 | a0001 | c0001 | t0018 | g0096 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01192 | hp1 | a0001 | c0002 | t0004 | g0124 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01243 | hp1 | a0001 | c0001 | t0037 | g0077 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01255 | hp1 | a0001 | c0001 | t0013 | g0211 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01256 | hp2 | a0001 | c0001 | t0032 | g0180 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01346 | hp2 | a0001 | c0001 | t0007 | g0073 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01361 | hp1 | a0001 | c0001 | t0011 | g0257 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01496 | hp1 | a0001 | c0002 | t0005 | g0009 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01516 | hp2 | a0001 | c0002 | t0005 | g0008 | EUR | IBS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0046 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01952 | hp2 | a0001 | c0001 | t0013 | g0207 | AMR | PEL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PEL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01978 | hp2 | a0001 | c0001 | t0013 | g0221 | AMR | PEL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02027 | hp2 | a0001 | c0002 | t0003 | g0021 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02040 | hp2 | a0001 | c0002 | t0003 | g0025 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02055 | hp2 | a0001 | c0001 | t0009 | g0144 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02129 | hp1 | a0001 | c0001 | t0035 | g0093 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02135 | hp2 | a0001 | c0002 | t0003 | g0024 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | CDX | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CDX | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0066 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02258 | hp1 | a0001 | c0001 | t0008 | g0113 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02258 | hp2 | a0001 | c0001 | t0009 | g0142 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0050 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02280 | hp2 | a0002 | c0005 | t0039 | g0042 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0065 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02451 | hp2 | a0001 | c0001 | t0028 | g0187 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02602 | hp1 | a0001 | c0001 | t0015 | g0109 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0122 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02615 | hp2 | a0001 | c0001 | t0008 | g0118 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02622 | hp2 | a0001 | c0001 | t0020 | g0004 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0063 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02698 | hp1 | a0001 | c0001 | t0012 | g0040 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02717 | hp2 | a0001 | c0001 | t0020 | g0038 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0047 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02735 | hp2 | a0001 | c0001 | t0027 | g0172 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0112 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02809 | hp2 | a0001 | c0001 | t0029 | g0156 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02818 | hp1 | a0001 | c0002 | t0004 | g0129 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02886 | hp1 | a0001 | c0001 | t0040 | g0148 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02895 | hp1 | a0001 | c0002 | t0004 | g0125 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02895 | hp2 | a0001 | c0001 | t0021 | g0075 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0062 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02897 | hp1 | a0001 | c0001 | t0021 | g0076 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0064 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02922 | hp2 | a0001 | c0002 | t0023 | g0005 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02965 | hp1 | a0001 | c0001 | t0019 | g0146 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02965 | hp2 | a0001 | c0001 | t0009 | g0138 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02970 | hp1 | a0001 | c0001 | t0036 | g0137 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0068 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0126 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03041 | hp2 | a0001 | c0001 | t0010 | g0074 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03098 | hp1 | a0001 | c0004 | t0004 | g0001 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0117 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03209 | hp1 | a0001 | c0002 | t0025 | g0149 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03225 | hp1 | a0001 | c0002 | t0005 | g0130 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0069 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03453 | hp1 | a0001 | c0002 | t0024 | g0123 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0048 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03486 | hp1 | a0001 | c0001 | t0041 | g0139 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0071 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0288 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03516 | hp2 | a0001 | c0002 | t0023 | g0006 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03540 | hp1 | a0001 | c0001 | t0009 | g0140 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0072 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03579 | hp1 | a0001 | c0001 | t0022 | g0059 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0049 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03669 | hp2 | a0001 | c0001 | t0012 | g0039 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | STU | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | STU | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0306 | SAS | BEB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0283 | SAS | BEB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | STU | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | STU | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18522 | hp1 | a0001 | c0002 | t0004 | g0121 | AFR | YRI | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | YRI | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18747 | hp1 | a0001 | c0001 | t0014 | g0267 | EAS | CHB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | YRI | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18906 | hp2 | a0001 | c0003 | t0017 | g0150 | AFR | YRI | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18939 | hp1 | a0001 | c0001 | t0034 | g0293 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18942 | hp1 | a0001 | c0002 | t0003 | g0020 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18943 | hp1 | a0001 | c0001 | t0033 | g0202 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18946 | hp2 | a0001 | c0001 | t0014 | g0268 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18952 | hp2 | a0001 | c0002 | t0003 | g0017 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18959 | hp1 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18960 | hp1 | a0001 | c0001 | t0031 | g0231 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18962 | hp2 | a0001 | c0002 | t0003 | g0035 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18969 | hp1 | a0001 | c0002 | t0003 | g0015 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18971 | hp1 | a0001 | c0001 | t0030 | g0169 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18971 | hp2 | a0001 | c0001 | t0011 | g0241 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18989 | hp2 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18991 | hp1 | a0001 | c0001 | t0011 | g0240 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18994 | hp1 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18999 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19000 | hp2 | a0001 | c0002 | t0003 | g0027 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19002 | hp2 | a0001 | c0002 | t0003 | g0013 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19009 | hp2 | a0001 | c0002 | t0003 | g0034 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19030 | hp1 | a0001 | c0001 | t0012 | g0152 | AFR | LWK | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | LWK | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0043 | AFR | LWK | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19043 | hp2 | a0001 | c0001 | t0016 | g0184 | AFR | LWK | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19057 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19060 | hp2 | a0001 | c0002 | t0003 | g0019 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19062 | hp2 | a0001 | c0002 | t0003 | g0023 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19065 | hp2 | a0001 | c0001 | t0011 | g0260 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19070 | hp2 | a0001 | c0001 | t0038 | g0292 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19085 | hp2 | a0001 | c0002 | t0003 | g0022 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19087 | hp2 | a0001 | c0002 | t0003 | g0029 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19091 | hp2 | a0001 | c0002 | t0003 | g0018 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0119 | AFR | YRI | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | YRI | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ASW | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA20129 | hp2 | a0001 | c0001 | t0010 | g0070 | AFR | ASW | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | GIH | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | GIH | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0012 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0141 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02486 | hp2 | a0001 | c0001 | t0019 | g0147 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0114 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0067 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | USA | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0045 | AFR | USA | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | USA | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | USA | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA21309 | hp1 | a0001 | c0001 | t0009 | g0143 | AFR | LWK | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0026 | g0271 | REF | REF | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0022 | g0061 | REF | REF | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:178877564
|
A | G | 1 | a0002 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.674A>G | p.Asn225Ser | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 9/20 | 933/7492 | 674/1752 | 225/583 | chr1 | 178877564 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:178776812
|
T | G | 2 | a0001c0002a0001c0004 | 46 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(43): Show |
synonymous_variant | LOW | c.48T>G | p.Thr16Thr | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/20 | 307/7492 | 48/1752 | 16/583 | chr1 | 178776812 | ||
| chr1:178877541
|
A | G | 1 | a0001c0003 | 2 | HG01099.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.651A>G | p.Pro217Pro | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 9/20 | 910/7492 | 651/1752 | 217/583 | chr1 | 178877541 | ||
| chr1:178878927
|
A | G | 1 | a0001c0004 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.771A>G | p.Gln257Gln | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/20 | 1030/7492 | 771/1752 | 257/583 | chr1 | 178878927 | ||
| chr1:178897669
|
A | T | 1 | a0002c0005 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.1437A>T | p.Ala479Ala | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/20 | 1696/7492 | 1437/1752 | 479/583 | chr1 | 178897669 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:178725264
|
A | AGCG | 1 | a0001c0001t0009 | 6 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-221_-219dupGGC | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/20 | 51480 | INFO_REALIGN_3_PRIME | chr1 | 178725264 | ||||
| chr1:178725264
|
A | AGCGGCAG others(2): Show |
1 | a0001c0001t0011 | 4 | HG01361.hp1 NA18971.hp2 NA18991.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-234_-233insAGCGGC others(3): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/20 | 51495 | INFO_REALIGN_3_PRIME | chr1 | 178725264 | ||||
| chr1:178725267
|
G | GGCA | 36 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(33): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
5_prime_UTR_variant | MODIFIER | c.-234_-233insAGC | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/20 | 51495 | INFO_REALIGN_3_PRIME | chr1 | 178725267 | ||||
| chr1:178725293
|
G | T | 3 | a0001c0001t0009a0001c0001t0021a0001c0001t0041 | 9 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-210G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/20 | 51472 | chr1 | 178725293 | |||||
| chr1:178916371
|
A | G | 2 | a0001c0001t0040a0002c0005t0039 | 2 | HG02280.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*12A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 12 | chr1 | 178916371 | |||||
| chr1:178916656
|
T | C | 1 | a0001c0001t0015 | 2 | HG00280.hp2 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*297T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 297 | chr1 | 178916656 | |||||
| chr1:178916745
|
A | C | 2 | a0001c0001t0040a0002c0005t0039 | 2 | HG02280.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*386A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 386 | chr1 | 178916745 | |||||
| chr1:178917054
|
C | T | 1 | a0001c0001t0013 | 4 | HG01106.hp1 HG01255.hp1 HG01952.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*695C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 695 | chr1 | 178917054 | |||||
| chr1:178917119
|
G | T | 1 | a0001c0001t0014 | 3 | HG00544.hp2 NA18747.hp1 NA18946.hp2 |
3_prime_UTR_variant | MODIFIER | c.*760G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 760 | chr1 | 178917119 | |||||
| chr1:178917783
|
T | C | 1 | a0001c0002t0003 | 22 | HG00544.hp1 HG00642.hp2 HG02027.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1424T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 1424 | chr1 | 178917783 | |||||
| chr1:178917869
|
T | C | 2 | a0001c0001t0040a0002c0005t0039 | 2 | HG02280.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1510T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 1510 | chr1 | 178917869 | |||||
| chr1:178917888
|
T | C | 6 | a0001c0002t0003a0001c0002t0004a0001c0002t0005others(3): Show | 43 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1529T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 1529 | chr1 | 178917888 | |||||
| chr1:178918050
|
A | G | 1 | a0001c0001t0020 | 2 | HG02622.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1691A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 1691 | chr1 | 178918050 | |||||
| chr1:178918073
|
A | T | 28 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(25): Show | 150 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(147): Show |
3_prime_UTR_variant | MODIFIER | c.*1714A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 1714 | chr1 | 178918073 | |||||
| chr1:178918345
|
A | C | 2 | a0001c0002t0005a0001c0002t0025 | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1986A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 1986 | chr1 | 178918345 | |||||
| chr1:178918347
|
T | C | 1 | a0001c0001t0020 | 2 | HG02622.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1988T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 1988 | chr1 | 178918347 | |||||
| chr1:178918391
|
A | T | 1 | a0001c0001t0038 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2032A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 2032 | chr1 | 178918391 | |||||
| chr1:178918428
|
C | T | 4 | a0001c0001t0006a0001c0001t0008a0001c0001t0009others(1): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2069C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 2069 | chr1 | 178918428 | |||||
| chr1:178918477
|
G | T | 4 | a0001c0001t0006a0001c0001t0008a0001c0001t0009others(1): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2118G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 2118 | chr1 | 178918477 | |||||
| chr1:178918619
|
C | T | 1 | a0001c0001t0033 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2260C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 2260 | chr1 | 178918619 | |||||
| chr1:178918847
|
A | G | 1 | a0001c0002t0024 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2488A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 2488 | chr1 | 178918847 | |||||
| chr1:178918983
|
A | G | 3 | a0001c0001t0008a0001c0001t0009a0001c0001t0041 | 13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2624A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 2624 | chr1 | 178918983 | |||||
| chr1:178919029
|
T | A | 1 | a0001c0001t0026 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2670T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 2670 | chr1 | 178919029 | |||||
| chr1:178919233
|
T | C | 1 | a0001c0001t0007 | 7 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2874T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 2874 | chr1 | 178919233 | |||||
| chr1:178919236
|
G | T | 1 | a0001c0001t0019 | 2 | HG02486.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2877G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 2877 | chr1 | 178919236 | |||||
| chr1:178919304
|
T | G | 1 | a0001c0003t0017 | 2 | HG01099.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2945T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 2945 | chr1 | 178919304 | |||||
| chr1:178919351
|
T | C | 1 | a0001c0001t0027 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2992T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 2992 | chr1 | 178919351 | |||||
| chr1:178919487
|
A | G | 1 | a0001c0001t0037 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3128A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 3128 | chr1 | 178919487 | |||||
| chr1:178919721
|
A | G | 30 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(27): Show | 152 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(149): Show |
3_prime_UTR_variant | MODIFIER | c.*3362A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 3362 | chr1 | 178919721 | |||||
| chr1:178919723
|
C | T | 2 | a0001c0001t0007a0001c0001t0010 | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3364C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 3364 | chr1 | 178919723 | |||||
| chr1:178919849
|
A | C | 1 | a0001c0001t0018 | 2 | HG01168.hp1 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3490A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 3490 | chr1 | 178919849 | |||||
| chr1:178919872
|
A | C | 1 | a0001c0001t0032 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3513A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 3513 | chr1 | 178919872 | |||||
| chr1:178919975
|
T | C | 1 | a0001c0001t0028 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3616T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 3616 | chr1 | 178919975 | |||||
| chr1:178920422
|
C | T | 1 | a0001c0001t0036 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4063C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 4063 | chr1 | 178920422 | |||||
| chr1:178920751
|
C | T | 1 | a0001c0001t0033 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4392C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 4392 | chr1 | 178920751 | |||||
| chr1:178920807
|
T | C | 1 | a0001c0001t0029 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4448T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 4448 | chr1 | 178920807 | |||||
| chr1:178920845
|
A | T | 1 | a0001c0001t0040 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4486A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 4486 | chr1 | 178920845 | |||||
| chr1:178920865
|
TTAAG | T | 4 | a0001c0002t0003a0001c0002t0004a0001c0002t0024others(1): Show | 34 | HG00544.hp1 HG00642.hp2 HG01070.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*4510_*4513delGTAA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 4510 | INFO_REALIGN_3_PRIME | chr1 | 178920865 | ||||
| chr1:178921129
|
T | C | 1 | a0001c0001t0034 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4770T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 4770 | chr1 | 178921129 | |||||
| chr1:178921408
|
T | C | 1 | a0001c0002t0025 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5049T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 5049 | chr1 | 178921408 | |||||
| chr1:178921415
|
G | A | 1 | a0001c0001t0035 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5056G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 5056 | chr1 | 178921415 | |||||
| chr1:178921517
|
G | A | 1 | a0001c0003t0017 | 2 | HG01099.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5158G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 5158 | chr1 | 178921517 | |||||
| chr1:178921564
|
C | T | 1 | a0001c0001t0020 | 2 | HG02622.hp2 HG02717.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5205C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 5205 | chr1 | 178921564 | |||||
| chr1:178921580
|
C | T | 1 | a0001c0001t0031 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5221C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 5221 | chr1 | 178921580 | |||||
| chr1:178921650
|
A | G | 7 | a0001c0001t0002a0001c0001t0015a0001c0001t0018others(4): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*5291A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 5291 | chr1 | 178921650 | |||||
| chr1:178921687
|
G | A | 1 | a0001c0001t0030 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5328G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 5328 | chr1 | 178921687 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:178725453
|
G | A | 1 | a0001c0004t0004g0001 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-84+34G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178725453 | ||||||
| chr1:178725689
|
C | T | 1 | a0001c0001t0002g0306 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-84+270C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178725689 | ||||||
| chr1:178725693
|
C | T | 154 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(151): Show | 154 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.-84+274C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178725693 | ||||||
| chr1:178725726
|
C | T | 1 | a0001c0001t0012g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-84+307C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178725726 | ||||||
| chr1:178725935
|
G | A | 154 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(151): Show | 154 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.-84+516G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178725935 | ||||||
| chr1:178725982
|
C | T | 6 | a0001c0001t0019g0146a0001c0001t0019g0147a0001c0001t0040g0148others(3): Show | 6 | HG01099.hp1 HG02486.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84+563C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178725982 | ||||||
| chr1:178726061
|
G | A | 1 | a0001c0001t0002g0153 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-84+642G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178726061 | ||||||
| chr1:178726335
|
C | G | 1 | a0001c0001t0001g0305 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-84+916C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178726335 | ||||||
| chr1:178726507
|
G | C | 3 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0020g0004 | 3 | HG02055.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-84+1088G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178726507 | ||||||
| chr1:178726542
|
T | TA | 40 | a0001c0001t0001g0155a0001c0001t0019g0146a0001c0001t0019g0147others(37): Show | 40 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.-84+1135dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178726542 | |||||
| chr1:178726555
|
C | A | 1 | a0001c0001t0001g0154 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-84+1136C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178726555 | ||||||
| chr1:178726850
|
A | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-84+1431A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178726850 | ||||||
| chr1:178726929
|
G | A | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-84+1510G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178726929 | ||||||
| chr1:178727042
|
G | A | 5 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(2): Show | 5 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-84+1623G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178727042 | ||||||
| chr1:178727195
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-84+1776A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178727195 | ||||||
| chr1:178727229
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-84+1810A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178727229 | ||||||
| chr1:178727230
|
C | CT | 8 | a0001c0001t0001g0303a0001c0001t0009g0138a0001c0001t0009g0140others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-84+1823dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178727230 | |||||
| chr1:178727230
|
CT | C | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-84+1823delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178727230 | |||||
| chr1:178727234
|
T | G | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-84+1815T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178727234 | ||||||
| chr1:178727309
|
C | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-84+1890C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178727309 | ||||||
| chr1:178727331
|
C | T | 6 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(3): Show | 6 | HG00438.hp1 HG00741.hp1 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84+1912C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178727331 | ||||||
| chr1:178727615
|
T | C | 168 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(165): Show | 168 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.-84+2196T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178727615 | ||||||
| chr1:178728151
|
ATGTT | A | 15 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-84+2735_-84+2738d others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178728151 | |||||
| chr1:178728321
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-84+2902A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178728321 | ||||||
| chr1:178728402
|
C | CT | 274 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.-84+2999dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178728402 | |||||
| chr1:178728402
|
C | CTT | 7 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(4): Show | 7 | HG04184.hp2 NA18964.hp2 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.-84+2998_-84+2999d others(4): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178728402 | |||||
| chr1:178728402
|
C | CTTTT | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-84+2996_-84+2999d others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178728402 | |||||
| chr1:178728513
|
A | T | 2 | a0001c0001t0001g0132a0001c0001t0002g0133 | 2 | HG01952.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.-84+3094A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178728513 | ||||||
| chr1:178728535
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-84+3116A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178728535 | ||||||
| chr1:178728588
|
A | G | 46 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(43): Show | 46 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.-84+3169A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178728588 | ||||||
| chr1:178728638
|
G | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-84+3219G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178728638 | ||||||
| chr1:178728684
|
T | C | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-84+3265T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178728684 | ||||||
| chr1:178728866
|
G | A | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-84+3447G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178728866 | ||||||
| chr1:178728917
|
T | C | 2 | a0001c0002t0023g0005a0001c0002t0023g0006 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-84+3498T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178728917 | ||||||
| chr1:178728961
|
A | G | 153 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(150): Show | 153 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.-84+3542A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178728961 | ||||||
| chr1:178729016
|
A | G | 303 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(300): Show | 303 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.-84+3597A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178729016 | ||||||
| chr1:178729201
|
T | G | 229 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(226): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-84+3782T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178729201 | ||||||
| chr1:178729390
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-84+3971C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178729390 | ||||||
| chr1:178729475
|
G | A | 2 | a0001c0001t0002g0078a0001c0001t0037g0077 | 2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-84+4056G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178729475 | ||||||
| chr1:178729500
|
A | T | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-84+4081A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178729500 | ||||||
| chr1:178729530
|
T | C | 10 | a0001c0001t0001g0157a0001c0002t0004g0120a0001c0002t0004g0121others(7): Show | 10 | HG00597.hp2 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-84+4111T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178729530 | ||||||
| chr1:178729540
|
A | G | 1 | a0001c0001t0001g0303 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-84+4121A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178729540 | ||||||
| chr1:178729569
|
C | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-84+4150C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178729569 | ||||||
| chr1:178729785
|
A | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84+4366A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178729785 | ||||||
| chr1:178729978
|
A | G | 5 | a0001c0001t0001g0060a0001c0001t0020g0004a0001c0001t0020g0038others(2): Show | 5 | HG01099.hp1 HG02523.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-84+4559A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178729978 | ||||||
| chr1:178730130
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-84+4711C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178730130 | ||||||
| chr1:178730131
|
G | T | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84+4712G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178730131 | ||||||
| chr1:178730191
|
C | T | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-84+4772C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178730191 | ||||||
| chr1:178730218
|
A | G | 2 | a0001c0002t0005g0036a0001c0002t0005g0037 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-84+4799A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178730218 | ||||||
| chr1:178730362
|
C | T | 63 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(60): Show | 63 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.-84+4943C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178730362 | ||||||
| chr1:178730396
|
G | A | 7 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(4): Show | 7 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-84+4977G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178730396 | ||||||
| chr1:178730556
|
A | AATTG | 25 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(22): Show | 25 | HG00738.hp2 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.-84+5139_-84+5142d others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178730556 | |||||
| chr1:178730573
|
T | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0297a0001c0001t0002g0079 | 3 | HG02083.hp1 HG02300.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-84+5154T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178730573 | ||||||
| chr1:178730573
|
TA | T | 29 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(26): Show | 29 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.-84+5166delA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178730573 | |||||
| chr1:178730615
|
T | C | 3 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045 | 3 | HG02886.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-84+5196T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178730615 | ||||||
| chr1:178730665
|
CT | C | 44 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(41): Show | 44 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.-84+5248delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178730665 | |||||
| chr1:178730690
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-84+5271T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178730690 | ||||||
| chr1:178730695
|
T | G | 1 | a0001c0002t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-84+5276T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178730695 | ||||||
| chr1:178730698
|
T | G | 10 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-84+5279T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178730698 | ||||||
| chr1:178730703
|
T | G | 1 | a0001c0001t0001g0160 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-84+5284T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178730703 | ||||||
| chr1:178730706
|
G | GT | 6 | a0001c0001t0001g0159a0001c0001t0002g0306a0001c0001t0019g0146others(3): Show | 6 | HG02135.hp1 HG02486.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-84+5298dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178730706 | |||||
| chr1:178730784
|
C | T | 5 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-84+5365C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178730784 | ||||||
| chr1:178730804
|
C | T | 1 | a0001c0002t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-84+5385C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178730804 | ||||||
| chr1:178730889
|
C | T | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-84+5470C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178730889 | ||||||
| chr1:178730890
|
G | A | 7 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(4): Show | 7 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-84+5471G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178730890 | ||||||
| chr1:178730989
|
C | T | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-84+5570C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178730989 | ||||||
| chr1:178731264
|
T | C | 1 | a0001c0002t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-84+5845T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178731264 | ||||||
| chr1:178731272
|
G | GT | 12 | a0001c0001t0001g0159a0001c0001t0001g0216a0001c0001t0001g0217others(9): Show | 12 | HG01978.hp2 HG02135.hp1 HG02293.hp1 others(9): Show |
intron_variant | MODIFIER | c.-84+5882dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178731272 | |||||
| chr1:178731272
|
G | GTTT | 28 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0060others(25): Show | 28 | HG00280.hp1 HG00423.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.-84+5880_-84+5882d others(5): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178731272 | |||||
| chr1:178731272
|
G | GTTTT | 36 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(33): Show | 36 | HG00438.hp2 HG00597.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.-84+5879_-84+5882d others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178731272 | |||||
| chr1:178731272
|
G | GTTTTT | 9 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0276others(6): Show | 9 | HG00544.hp2 HG01884.hp2 HG03579.hp1 others(6): Show |
intron_variant | MODIFIER | c.-84+5878_-84+5882d others(7): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178731272 | |||||
| chr1:178731272
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0019g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-84+5873_-84+5882d others(12): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178731272 | |||||
| chr1:178731272
|
GT | G | 52 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0162others(49): Show | 52 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.-84+5882delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178731272 | |||||
| chr1:178731272
|
GTT | G | 36 | a0001c0001t0001g0161a0001c0001t0006g0044a0001c0001t0006g0045others(33): Show | 36 | HG00558.hp2 HG00642.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.-84+5881_-84+5882d others(4): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178731272 | |||||
| chr1:178731272
|
GTTT | G | 31 | a0001c0001t0002g0079a0001c0001t0002g0100a0001c0001t0002g0101others(28): Show | 31 | HG00280.hp2 HG00642.hp1 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.-84+5880_-84+5882d others(5): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178731272 | |||||
| chr1:178731272
|
GTTTT | G | 40 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(37): Show | 40 | HG00639.hp2 HG00741.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.-84+5879_-84+5882d others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178731272 | |||||
| chr1:178731272
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0002g0287 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-84+5873_-84+5882d others(12): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178731272 | |||||
| chr1:178731272
|
GTTTTTTT others(6): Show |
G | 5 | a0001c0001t0006g0046a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-84+5870_-84+5882d others(15): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178731272 | |||||
| chr1:178731278
|
T | G | 1 | a0001c0001t0001g0051 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-84+5859T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178731278 | ||||||
| chr1:178731323
|
C | G | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-84+5904C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178731323 | ||||||
| chr1:178731336
|
G | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-84+5917G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178731336 | ||||||
| chr1:178731432
|
G | A | 5 | a0001c0001t0006g0046a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-84+6013G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178731432 | ||||||
| chr1:178731535
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-84+6116G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178731535 | ||||||
| chr1:178731538
|
C | T | 1 | a0001c0001t0001g0272 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-84+6119C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178731538 | ||||||
| chr1:178731662
|
C | T | 1 | a0001c0001t0026g0271 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-84+6243C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178731662 | ||||||
| chr1:178731700
|
A | G | 15 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-84+6281A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178731700 | ||||||
| chr1:178731775
|
C | G | 1 | a0001c0001t0001g0183 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-84+6356C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178731775 | ||||||
| chr1:178731934
|
G | A | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-84+6515G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178731934 | ||||||
| chr1:178731948
|
C | T | 1 | a0001c0001t0001g0215 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-84+6529C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178731948 | ||||||
| chr1:178731954
|
C | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-84+6535C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178731954 | ||||||
| chr1:178732008
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-84+6589A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178732008 | ||||||
| chr1:178732033
|
A | C | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84+6614A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178732033 | ||||||
| chr1:178732115
|
C | CATCATCT others(14): Show |
2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-84+6699_-84+6719d others(23): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178732115 | |||||
| chr1:178732236
|
G | A | 1 | a0001c0001t0016g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-84+6817G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178732236 | ||||||
| chr1:178732293
|
T | TTTTATTT others(1): Show |
83 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(80): Show | 83 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.-84+6890_-84+6897d others(10): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178732293 | |||||
| chr1:178732293
|
T | TTTTATTT others(5): Show |
4 | a0001c0001t0002g0100a0001c0001t0040g0148a0001c0002t0005g0130others(1): Show | 4 | HG02886.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-84+6886_-84+6897d others(14): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178732293 | |||||
| chr1:178732293
|
T | TTTTATTT others(9): Show |
40 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(37): Show | 40 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.-84+6882_-84+6897d others(18): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178732293 | |||||
| chr1:178732293
|
T | TTTTATTT others(13): Show |
2 | a0001c0002t0004g0129a0001c0002t0005g0007 | 2 | HG00099.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-84+6878_-84+6897d others(22): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178732293 | |||||
| chr1:178732293
|
TTTTA | T | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84+6894_-84+6897d others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178732293 | |||||
| chr1:178732293
|
TTTTATTT others(1): Show |
T | 15 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-84+6890_-84+6897d others(10): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178732293 | |||||
| chr1:178732445
|
C | G | 1 | a0001c0001t0026g0271 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-84+7026C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178732445 | ||||||
| chr1:178732523
|
T | C | 2 | a0001c0001t0021g0075a0001c0001t0021g0076 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-84+7104T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178732523 | ||||||
| chr1:178732577
|
G | A | 1 | a0001c0001t0008g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-84+7158G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178732577 | ||||||
| chr1:178732636
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-84+7217A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178732636 | ||||||
| chr1:178732732
|
GT | G | 15 | a0001c0001t0001g0223a0001c0001t0007g0064a0001c0001t0007g0065others(12): Show | 15 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.-84+7328delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178732732 | |||||
| chr1:178732821
|
T | C | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-84+7402T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178732821 | ||||||
| chr1:178732916
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-84+7497C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178732916 | ||||||
| chr1:178732917
|
G | T | 10 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-84+7498G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178732917 | ||||||
| chr1:178733045
|
T | C | 3 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0145 | 3 | HG00558.hp1 HG02040.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-84+7626T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178733045 | ||||||
| chr1:178733075
|
C | T | 5 | a0001c0002t0003g0027a0001c0002t0003g0033a0001c0002t0003g0034others(2): Show | 5 | HG02818.hp1 NA18962.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-84+7656C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178733075 | ||||||
| chr1:178733076
|
G | A | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-84+7657G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178733076 | ||||||
| chr1:178733281
|
G | T | 62 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(59): Show | 62 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.-84+7862G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178733281 | ||||||
| chr1:178733658
|
A | G | 2 | a0001c0002t0004g0127a0001c0002t0004g0128 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-84+8239A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178733658 | ||||||
| chr1:178733740
|
G | A | 152 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(149): Show | 152 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-84+8321G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178733740 | ||||||
| chr1:178733779
|
G | A | 1 | a0001c0001t0037g0077 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-84+8360G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178733779 | ||||||
| chr1:178733945
|
A | T | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-84+8526A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178733945 | ||||||
| chr1:178734020
|
T | C | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-84+8601T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178734020 | ||||||
| chr1:178734094
|
A | G | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-84+8675A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178734094 | ||||||
| chr1:178734111
|
A | G | 35 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(32): Show | 35 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-84+8692A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178734111 | ||||||
| chr1:178734152
|
C | G | 1 | a0002c0005t0039g0042 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-84+8733C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178734152 | ||||||
| chr1:178734331
|
C | T | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-84+8912C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178734331 | ||||||
| chr1:178734366
|
A | T | 1 | a0001c0002t0025g0149 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-84+8947A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178734366 | ||||||
| chr1:178734369
|
T | C | 1 | a0001c0001t0026g0271 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-84+8950T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178734369 | ||||||
| chr1:178734777
|
A | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84+9358A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178734777 | ||||||
| chr1:178734782
|
G | A | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84+9363G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178734782 | ||||||
| chr1:178734841
|
A | T | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-84+9422A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178734841 | ||||||
| chr1:178735431
|
C | CT | 89 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(86): Show | 89 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-84+10028dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178735431 | |||||
| chr1:178735431
|
CT | C | 9 | a0001c0001t0002g0134a0001c0001t0012g0039a0001c0001t0012g0040others(6): Show | 9 | HG00738.hp2 HG01099.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-84+10028delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178735431 | |||||
| chr1:178735436
|
T | C | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-84+10017T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178735436 | ||||||
| chr1:178735552
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-84+10133T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178735552 | ||||||
| chr1:178735571
|
G | A | 10 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-84+10152G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178735571 | ||||||
| chr1:178735599
|
TTC | T | 17 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(14): Show | 17 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-84+10182_-84+1018 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178735599 | |||||
| chr1:178735600
|
TC | T | 129 | a0001c0001t0001g0132a0001c0001t0001g0244a0001c0001t0002g0002others(126): Show | 129 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.-84+10182delC | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178735600 | ||||||
| chr1:178735601
|
C | CT | 7 | a0001c0001t0001g0243a0001c0001t0001g0270a0001c0001t0001g0278others(4): Show | 7 | HG00438.hp1 NA18973.hp2 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.-84+10203dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178735601 | |||||
| chr1:178735601
|
C | T | 7 | a0001c0001t0002g0099a0001c0001t0002g0111a0001c0001t0021g0075others(4): Show | 7 | HG00642.hp2 HG01361.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-84+10182C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178735601 | ||||||
| chr1:178735601
|
CT | C | 8 | a0001c0001t0001g0163a0001c0001t0001g0185a0001c0001t0001g0186others(5): Show | 8 | HG01256.hp1 HG02896.hp2 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.-84+10203delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178735601 | |||||
| chr1:178735638
|
C | T | 2 | a0001c0001t0021g0075a0001c0001t0021g0076 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-84+10219C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178735638 | ||||||
| chr1:178735673
|
T | A | 1 | a0001c0002t0003g0013 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-84+10254T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178735673 | ||||||
| chr1:178735774
|
A | G | 63 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(60): Show | 63 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.-84+10355A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178735774 | ||||||
| chr1:178735889
|
CATT | C | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-84+10474_-84+1047 others(7): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178735889 | |||||
| chr1:178736032
|
AGTAT | A | 45 | a0001c0001t0001g0244a0001c0002t0003g0013a0001c0002t0003g0014others(42): Show | 45 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-84+10616_-84+1061 others(8): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178736032 | |||||
| chr1:178736165
|
G | T | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84+10746G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178736165 | ||||||
| chr1:178736165
|
GT | G | 7 | a0001c0001t0001g0051a0001c0001t0001g0165a0001c0001t0012g0152others(4): Show | 7 | HG01070.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-84+10762delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178736165 | |||||
| chr1:178736181
|
T | C | 56 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.-84+10762T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178736181 | ||||||
| chr1:178736181
|
T | TC | 7 | a0001c0001t0002g0110a0001c0001t0002g0115a0001c0001t0002g0291others(4): Show | 7 | HG01978.hp1 NA18939.hp1 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.-84+10763dupC | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178736181 | |||||
| chr1:178736233
|
G | T | 28 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0154others(25): Show | 28 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.-84+10814G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178736233 | ||||||
| chr1:178736241
|
G | A | 36 | a0001c0001t0001g0244a0001c0002t0003g0013a0001c0002t0003g0014others(33): Show | 36 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.-84+10822G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178736241 | ||||||
| chr1:178736296
|
A | G | 290 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(287): Show | 290 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.-84+10877A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178736296 | ||||||
| chr1:178736414
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-84+10995G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178736414 | ||||||
| chr1:178736415
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-84+10996G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178736415 | ||||||
| chr1:178736529
|
C | T | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-84+11110C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178736529 | ||||||
| chr1:178736623
|
T | C | 10 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-84+11204T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178736623 | ||||||
| chr1:178736735
|
C | CA | 6 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-84+11323dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178736735 | |||||
| chr1:178736888
|
C | T | 1 | a0001c0001t0006g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-84+11469C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178736888 | ||||||
| chr1:178736975
|
A | G | 24 | a0001c0001t0001g0244a0001c0002t0003g0013a0001c0002t0003g0014others(21): Show | 24 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.-84+11556A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178736975 | ||||||
| chr1:178736976
|
C | G | 5 | a0001c0001t0006g0046a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-84+11557C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178736976 | ||||||
| chr1:178737248
|
C | T | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-84+11829C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178737248 | ||||||
| chr1:178737249
|
G | A | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-84+11830G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178737249 | ||||||
| chr1:178737302
|
G | A | 3 | a0001c0001t0019g0146a0001c0001t0019g0147a0001c0002t0005g0007 | 3 | HG00099.hp1 HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-84+11883G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178737302 | ||||||
| chr1:178737369
|
G | A | 1 | a0001c0002t0025g0149 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-84+11950G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178737369 | ||||||
| chr1:178737376
|
G | A | 1 | a0001c0001t0011g0260 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-84+11957G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178737376 | ||||||
| chr1:178737422
|
A | G | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-84+12003A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178737422 | ||||||
| chr1:178737440
|
G | A | 50 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0160others(47): Show | 50 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.-84+12021G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178737440 | ||||||
| chr1:178737497
|
C | T | 2 | a0001c0002t0004g0127a0001c0002t0004g0128 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-84+12078C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178737497 | ||||||
| chr1:178737618
|
C | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-84+12199C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178737618 | ||||||
| chr1:178737817
|
A | G | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-84+12398A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178737817 | ||||||
| chr1:178737858
|
G | T | 1 | a0001c0002t0005g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-84+12439G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178737858 | ||||||
| chr1:178738175
|
TCA | T | 50 | a0001c0001t0001g0155a0001c0001t0001g0158a0001c0001t0001g0160others(47): Show | 50 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.-84+12757_-84+1275 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178738175 | ||||||
| chr1:178738203
|
C | CT | 19 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0181others(16): Show | 19 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.-84+12807dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178738203 | |||||
| chr1:178738203
|
C | CTT | 9 | a0001c0001t0001g0162a0001c0001t0006g0043a0001c0001t0006g0044others(6): Show | 9 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-84+12806_-84+1280 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178738203 | |||||
| chr1:178738203
|
CT | C | 28 | a0001c0001t0001g0164a0001c0001t0002g0078a0001c0001t0002g0291others(25): Show | 28 | HG00738.hp2 HG01099.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.-84+12807delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178738203 | |||||
| chr1:178738397
|
CAG | C | 3 | a0001c0001t0009g0141a0001c0001t0009g0142a0001c0001t0009g0143 | 3 | HG02258.hp2 HG02486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-84+12981_-84+1298 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178738397 | |||||
| chr1:178738563
|
T | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0216 | 2 | HG02135.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-84+13144T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178738563 | ||||||
| chr1:178738675
|
A | G | 1 | a0001c0001t0008g0112 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-84+13256A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178738675 | ||||||
| chr1:178738851
|
G | C | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84+13432G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178738851 | ||||||
| chr1:178738906
|
T | C | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-84+13487T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178738906 | ||||||
| chr1:178739585
|
G | C | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-84+14166G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178739585 | ||||||
| chr1:178739822
|
A | G | 3 | a0001c0001t0001g0223a0001c0001t0001g0238a0001c0001t0001g0239 | 3 | NA18939.hp2 NA18953.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.-84+14403A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178739822 | ||||||
| chr1:178739895
|
G | A | 1 | a0001c0001t0012g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-84+14476G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178739895 | ||||||
| chr1:178740564
|
A | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84+15145A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178740564 | ||||||
| chr1:178740612
|
T | C | 7 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(4): Show | 7 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-84+15193T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178740612 | ||||||
| chr1:178740671
|
T | C | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-84+15252T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178740671 | ||||||
| chr1:178740745
|
C | T | 2 | a0001c0001t0001g0060a0001c0001t0001g0145 | 2 | HG00558.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-84+15326C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178740745 | ||||||
| chr1:178740831
|
C | T | 63 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(60): Show | 63 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.-84+15412C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178740831 | ||||||
| chr1:178740863
|
C | A | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-84+15444C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178740863 | ||||||
| chr1:178740998
|
G | A | 1 | a0001c0001t0014g0275 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-84+15579G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178740998 | ||||||
| chr1:178741021
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-84+15602G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178741021 | ||||||
| chr1:178741025
|
CAT | C | 25 | a0001c0001t0001g0055a0001c0001t0001g0244a0001c0002t0003g0013others(22): Show | 25 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.-84+15611_-84+1561 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178741025 | |||||
| chr1:178741154
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-84+15735T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178741154 | ||||||
| chr1:178741477
|
T | C | 1 | a0001c0001t0001g0303 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-84+16058T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178741477 | ||||||
| chr1:178741647
|
C | T | 2 | a0001c0001t0001g0237a0001c0001t0001g0259 | 2 | HG02293.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-84+16228C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178741647 | ||||||
| chr1:178741653
|
A | G | 2 | a0001c0001t0001g0242a0001c0001t0001g0269 | 2 | HG00423.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-84+16234A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178741653 | ||||||
| chr1:178741797
|
A | G | 1 | a0001c0001t0015g0109 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-84+16378A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178741797 | ||||||
| chr1:178741809
|
A | G | 63 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(60): Show | 63 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.-84+16390A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178741809 | ||||||
| chr1:178741909
|
G | A | 3 | a0001c0001t0001g0270a0001c0001t0001g0278a0001c0002t0005g0130 | 3 | HG03225.hp1 NA18995.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-84+16490G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178741909 | ||||||
| chr1:178742008
|
C | T | 5 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(2): Show | 5 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.-84+16589C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178742008 | ||||||
| chr1:178742078
|
G | C | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-84+16659G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178742078 | ||||||
| chr1:178742091
|
G | A | 2 | a0001c0001t0001g0215a0001c0001t0001g0285 | 2 | NA18967.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.-84+16672G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178742091 | ||||||
| chr1:178742110
|
T | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0194 | 2 | HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-84+16691T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178742110 | ||||||
| chr1:178742132
|
C | CA | 49 | a0001c0001t0001g0057a0001c0001t0001g0155a0001c0001t0001g0158others(46): Show | 49 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.-84+16732dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178742132 | |||||
| chr1:178742132
|
C | CAA | 12 | a0001c0001t0001g0167a0001c0001t0001g0195a0001c0001t0001g0220others(9): Show | 12 | HG01099.hp1 HG01106.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-84+16731_-84+1673 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178742132 | |||||
| chr1:178742132
|
CA | C | 9 | a0001c0001t0019g0146a0001c0001t0026g0271a0001c0002t0005g0007others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-84+16732delA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178742132 | |||||
| chr1:178742149
|
A | AG | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-84+16730_-84+1673 others(5): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178742149 | ||||||
| chr1:178742149
|
A | G | 4 | a0001c0001t0001g0249a0001c0001t0012g0152a0001c0001t0021g0075others(1): Show | 4 | HG01192.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-84+16730A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178742149 | ||||||
| chr1:178742159
|
A | C | 10 | a0001c0001t0001g0060a0001c0001t0001g0145a0001c0001t0008g0112others(7): Show | 10 | HG00558.hp1 HG02258.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.-84+16740A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178742159 | ||||||
| chr1:178742177
|
T | C | 15 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-84+16758T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178742177 | ||||||
| chr1:178742190
|
C | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-84+16771C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178742190 | ||||||
| chr1:178742281
|
T | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-84+16862T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178742281 | ||||||
| chr1:178742309
|
T | G | 1 | a0001c0001t0001g0196 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-84+16890T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178742309 | ||||||
| chr1:178742418
|
A | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0191 | 2 | NA18941.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.-84+16999A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178742418 | ||||||
| chr1:178742541
|
A | G | 1 | a0001c0001t0001g0204 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-84+17122A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178742541 | ||||||
| chr1:178742551
|
G | C | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-84+17132G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178742551 | ||||||
| chr1:178742552
|
A | G | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-84+17133A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178742552 | ||||||
| chr1:178742919
|
A | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84+17500A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178742919 | ||||||
| chr1:178743065
|
A | T | 1 | a0001c0001t0002g0079 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-84+17646A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178743065 | ||||||
| chr1:178743084
|
TGGTGACA others(14): Show |
T | 1 | a0001c0001t0001g0304 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-84+17666_-84+1768 others(25): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178743084 | ||||||
| chr1:178743182
|
G | A | 2 | a0001c0001t0002g0083a0001c0001t0002g0131 | 2 | HG01099.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-84+17763G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178743182 | ||||||
| chr1:178743383
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-84+17964A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178743383 | ||||||
| chr1:178743696
|
A | C | 5 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-84+18277A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178743696 | ||||||
| chr1:178744084
|
A | G | 6 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-84+18665A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178744084 | ||||||
| chr1:178744330
|
C | T | 1 | a0001c0001t0015g0108 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-84+18911C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178744330 | ||||||
| chr1:178744462
|
T | G | 1 | a0001c0001t0001g0162 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-84+19043T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178744462 | ||||||
| chr1:178744488
|
G | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-84+19069G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178744488 | ||||||
| chr1:178744538
|
G | T | 1 | a0001c0001t0007g0073 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-84+19119G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178744538 | ||||||
| chr1:178744670
|
A | T | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84+19251A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178744670 | ||||||
| chr1:178744673
|
G | A | 1 | a0001c0001t0026g0271 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-84+19254G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178744673 | ||||||
| chr1:178744699
|
C | T | 63 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(60): Show | 63 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.-84+19280C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178744699 | ||||||
| chr1:178744764
|
G | A | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-84+19345G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178744764 | ||||||
| chr1:178744796
|
C | T | 1 | a0001c0001t0008g0112 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-84+19377C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178744796 | ||||||
| chr1:178744817
|
C | CA | 24 | a0001c0001t0001g0192a0001c0001t0001g0224a0001c0001t0001g0252others(21): Show | 24 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(21): Show |
intron_variant | MODIFIER | c.-84+19418dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178744817 | |||||
| chr1:178744817
|
C | CAAA | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0019g0147others(3): Show | 6 | HG01099.hp1 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84+19416_-84+1941 others(7): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178744817 | |||||
| chr1:178744817
|
CA | C | 65 | a0001c0001t0001g0055a0001c0001t0001g0176a0001c0001t0001g0286others(62): Show | 65 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.-84+19418delA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178744817 | |||||
| chr1:178744817
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-84+19408_-84+1941 others(15): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178744817 | |||||
| chr1:178744834
|
A | G | 1 | a0001c0001t0015g0109 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-84+19415A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178744834 | ||||||
| chr1:178744894
|
G | A | 12 | a0001c0002t0004g0012a0001c0002t0004g0120a0001c0002t0004g0121others(9): Show | 12 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.-84+19475G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178744894 | ||||||
| chr1:178745044
|
A | G | 1 | a0001c0001t0008g0118 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-84+19625A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178745044 | ||||||
| chr1:178745182
|
A | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84+19763A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178745182 | ||||||
| chr1:178745251
|
GGGGGAAT others(4): Show |
G | 9 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(6): Show | 9 | HG01069.hp1 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-84+19833_-84+1984 others(15): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178745251 | ||||||
| chr1:178745296
|
T | C | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-84+19877T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178745296 | ||||||
| chr1:178745305
|
C | T | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-84+19886C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178745305 | ||||||
| chr1:178745342
|
A | G | 4 | a0001c0001t0001g0229a0001c0001t0001g0235a0001c0001t0001g0236others(1): Show | 4 | HG01243.hp2 HG01257.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.-84+19923A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178745342 | ||||||
| chr1:178745550
|
G | C | 1 | a0001c0001t0001g0285 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-84+20131G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178745550 | ||||||
| chr1:178745561
|
A | G | 2 | a0001c0002t0003g0023a0001c0002t0003g0025 | 2 | HG02040.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-84+20142A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178745561 | ||||||
| chr1:178745606
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-84+20187A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178745606 | ||||||
| chr1:178745633
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-84+20214A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178745633 | ||||||
| chr1:178745688
|
C | G | 1 | a0001c0001t0011g0257 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-84+20269C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178745688 | ||||||
| chr1:178745728
|
A | G | 1 | a0001c0001t0006g0044 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-84+20309A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178745728 | ||||||
| chr1:178745822
|
C | CT | 24 | a0001c0001t0001g0060a0001c0001t0001g0189a0001c0001t0001g0190others(21): Show | 24 | HG01346.hp2 HG01358.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.-84+20427dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178745822 | |||||
| chr1:178745822
|
CT | C | 112 | a0001c0001t0001g0055a0001c0001t0001g0132a0001c0001t0001g0217others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-84+20427delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178745822 | |||||
| chr1:178745822
|
CTT | C | 7 | a0001c0001t0002g0084a0001c0001t0002g0296a0001c0001t0020g0004others(4): Show | 7 | HG01074.hp1 HG01099.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-84+20426_-84+2042 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178745822 | |||||
| chr1:178745822
|
CTTTTTTT others(6): Show |
C | 15 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-84+20415_-84+2042 others(17): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178745822 | |||||
| chr1:178745861
|
C | T | 7 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(4): Show | 7 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-84+20442C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178745861 | ||||||
| chr1:178745865
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-84+20446C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178745865 | ||||||
| chr1:178746009
|
A | T | 2 | a0001c0001t0001g0228a0001c0001t0001g0234 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-84+20590A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178746009 | ||||||
| chr1:178746045
|
C | T | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-84+20626C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178746045 | ||||||
| chr1:178746226
|
T | C | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-84+20807T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178746226 | ||||||
| chr1:178746300
|
C | A | 1 | a0001c0002t0005g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-84+20881C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178746300 | ||||||
| chr1:178746301
|
G | A | 2 | a0001c0002t0023g0005a0001c0002t0023g0006 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-84+20882G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178746301 | ||||||
| chr1:178746564
|
G | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-84+21145G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178746564 | ||||||
| chr1:178746686
|
G | C | 1 | a0001c0001t0006g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-84+21267G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178746686 | ||||||
| chr1:178746871
|
T | G | 2 | a0001c0001t0018g0080a0001c0001t0018g0096 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-84+21452T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178746871 | ||||||
| chr1:178747021
|
T | A | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-84+21602T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178747021 | ||||||
| chr1:178747028
|
G | A | 73 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.-84+21609G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178747028 | ||||||
| chr1:178747079
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-84+21660C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178747079 | ||||||
| chr1:178747159
|
C | G | 35 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(32): Show | 35 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-84+21740C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178747159 | ||||||
| chr1:178747165
|
G | C | 2 | a0001c0002t0004g0012a0001c0002t0004g0129 | 2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-84+21746G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178747165 | ||||||
| chr1:178747261
|
A | G | 4 | a0001c0001t0001g0229a0001c0001t0001g0235a0001c0001t0001g0236others(1): Show | 4 | HG01243.hp2 HG01257.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.-84+21842A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178747261 | ||||||
| chr1:178747382
|
T | C | 19 | a0001c0001t0001g0154a0001c0001t0001g0157a0001c0001t0001g0242others(16): Show | 19 | HG00280.hp1 HG00423.hp2 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.-84+21963T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178747382 | ||||||
| chr1:178747392
|
G | A | 1 | a0001c0002t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-84+21973G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178747392 | ||||||
| chr1:178747581
|
G | A | 3 | a0001c0001t0010g0068a0001c0001t0010g0069a0001c0001t0010g0070 | 3 | HG02976.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-84+22162G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178747581 | ||||||
| chr1:178747691
|
A | G | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-84+22272A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178747691 | ||||||
| chr1:178747694
|
G | A | 63 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(60): Show | 63 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.-84+22275G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178747694 | ||||||
| chr1:178747776
|
C | T | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0284 | 3 | NA18747.hp2 NA19067.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-84+22357C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178747776 | ||||||
| chr1:178747777
|
G | A | 1 | a0001c0002t0005g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-84+22358G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178747777 | ||||||
| chr1:178747813
|
G | A | 1 | a0001c0002t0005g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-84+22394G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178747813 | ||||||
| chr1:178747920
|
A | G | 1 | a0001c0002t0005g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-84+22501A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178747920 | ||||||
| chr1:178747992
|
C | G | 15 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-84+22573C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178747992 | ||||||
| chr1:178748086
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-84+22667G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178748086 | ||||||
| chr1:178748148
|
T | C | 13 | a0001c0001t0001g0193a0001c0001t0001g0209a0001c0001t0001g0210others(10): Show | 13 | HG01106.hp1 HG01255.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.-84+22729T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178748148 | ||||||
| chr1:178748283
|
G | A | 15 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-84+22864G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178748283 | ||||||
| chr1:178748290
|
A | T | 2 | a0001c0002t0005g0036a0001c0002t0005g0037 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-84+22871A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178748290 | ||||||
| chr1:178748319
|
C | CA | 12 | a0001c0001t0001g0235a0001c0001t0001g0244a0001c0001t0006g0043others(9): Show | 12 | HG01496.hp2 HG01884.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-84+22916dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178748319 | |||||
| chr1:178748319
|
CA | C | 9 | a0001c0001t0001g0053a0001c0001t0001g0250a0001c0001t0001g0251others(6): Show | 9 | HG01496.hp1 HG02040.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.-84+22916delA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178748319 | |||||
| chr1:178748422
|
T | C | 1 | a0001c0001t0001g0225 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-84+23003T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178748422 | ||||||
| chr1:178748517
|
A | G | 1 | a0001c0002t0005g0011 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-84+23098A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178748517 | ||||||
| chr1:178748546
|
T | C | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-84+23127T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178748546 | ||||||
| chr1:178748725
|
C | T | 2 | a0001c0001t0001g0233a0001c0001t0001g0304 | 2 | HG01169.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.-84+23306C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178748725 | ||||||
| chr1:178748808
|
G | A | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-84+23389G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178748808 | ||||||
| chr1:178748850
|
C | CA | 72 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(69): Show | 72 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-84+23447dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178748850 | |||||
| chr1:178748850
|
C | CAA | 46 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(43): Show | 46 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.-84+23446_-84+2344 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178748850 | |||||
| chr1:178748937
|
G | A | 1 | a0001c0001t0006g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-84+23518G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178748937 | ||||||
| chr1:178749028
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-84+23609G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178749028 | ||||||
| chr1:178749079
|
C | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-84+23660C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178749079 | ||||||
| chr1:178749114
|
T | C | 5 | a0001c0001t0006g0046a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-84+23695T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178749114 | ||||||
| chr1:178749121
|
T | C | 15 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-84+23702T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178749121 | ||||||
| chr1:178749174
|
C | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-84+23755C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178749174 | ||||||
| chr1:178749401
|
A | G | 106 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(103): Show | 106 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.-84+23982A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178749401 | ||||||
| chr1:178749606
|
T | C | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-84+24187T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178749606 | ||||||
| chr1:178749606
|
T | G | 2 | a0001c0002t0004g0127a0001c0002t0004g0128 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-84+24187T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178749606 | ||||||
| chr1:178749621
|
C | T | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-84+24202C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178749621 | ||||||
| chr1:178749696
|
T | C | 7 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(4): Show | 7 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-84+24277T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178749696 | ||||||
| chr1:178749819
|
G | T | 37 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(34): Show | 37 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.-84+24400G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178749819 | ||||||
| chr1:178749991
|
G | A | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84+24572G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178749991 | ||||||
| chr1:178750070
|
C | T | 7 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(4): Show | 7 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.-84+24651C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178750070 | ||||||
| chr1:178750129
|
A | C | 1 | a0001c0001t0022g0059 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-84+24710A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178750129 | ||||||
| chr1:178750171
|
C | T | 57 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(54): Show | 57 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.-84+24752C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178750171 | ||||||
| chr1:178750189
|
T | C | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-84+24770T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178750189 | ||||||
| chr1:178750616
|
G | A | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-84+25197G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178750616 | ||||||
| chr1:178750663
|
T | TTTTTTTT others(186): Show |
1 | a0001c0001t0001g0302 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-84+25249_-84+2525 others(197): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178750663 | |||||
| chr1:178750809
|
A | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-84+25390A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178750809 | ||||||
| chr1:178751115
|
CACACACA others(3): Show |
C | 15 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-83-25557_-83-2554 others(14): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178751115 | |||||
| chr1:178751287
|
A | G | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-83-25395A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178751287 | ||||||
| chr1:178751399
|
A | T | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-83-25283A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178751399 | ||||||
| chr1:178751491
|
C | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-83-25191C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178751491 | ||||||
| chr1:178751492
|
C | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-83-25190C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178751492 | ||||||
| chr1:178751935
|
G | A | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-83-24747G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178751935 | ||||||
| chr1:178752067
|
G | T | 1 | a0001c0001t0006g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-83-24615G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178752067 | ||||||
| chr1:178752133
|
A | AT | 17 | a0001c0001t0001g0216a0001c0001t0002g0079a0001c0001t0006g0043others(14): Show | 17 | HG01884.hp1 HG02083.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.-83-24531dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178752133 | |||||
| chr1:178752133
|
AT | A | 26 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(23): Show | 26 | HG00544.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.-83-24531delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178752133 | |||||
| chr1:178752287
|
G | T | 1 | a0001c0001t0001g0174 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-83-24395G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178752287 | ||||||
| chr1:178752317
|
A | AT | 73 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0297others(70): Show | 73 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.-83-24352dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178752317 | |||||
| chr1:178752342
|
T | TG | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01099.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-83-24338dupG | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178752342 | |||||
| chr1:178752345
|
C | G | 19 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(16): Show | 19 | HG01099.hp1 HG01884.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-83-24337C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178752345 | ||||||
| chr1:178752346
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-83-24336G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178752346 | ||||||
| chr1:178752348
|
G | C | 2 | a0001c0001t0001g0194a0001c0002t0004g0129 | 2 | HG02818.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-83-24334G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178752348 | ||||||
| chr1:178752348
|
G | T | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-83-24334G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178752348 | ||||||
| chr1:178752592
|
G | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0216 | 2 | HG02135.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-83-24090G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178752592 | ||||||
| chr1:178752670
|
A | G | 43 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(40): Show | 43 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.-83-24012A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178752670 | ||||||
| chr1:178752673
|
T | G | 1 | a0001c0002t0003g0026 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-83-24009T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178752673 | ||||||
| chr1:178752821
|
G | T | 27 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(24): Show | 27 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.-83-23861G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178752821 | ||||||
| chr1:178753104
|
C | T | 7 | a0001c0001t0002g0082a0001c0001t0002g0094a0001c0001t0002g0095others(4): Show | 7 | NA18959.hp2 NA18966.hp1 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.-83-23578C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178753104 | ||||||
| chr1:178753358
|
G | A | 1 | a0001c0001t0001g0174 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-83-23324G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178753358 | ||||||
| chr1:178753361
|
A | G | 305 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.-83-23321A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178753361 | ||||||
| chr1:178753366
|
A | T | 1 | a0001c0001t0019g0147 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-83-23316A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178753366 | ||||||
| chr1:178753367
|
A | G | 5 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-83-23315A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178753367 | ||||||
| chr1:178753548
|
A | G | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-83-23134A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178753548 | ||||||
| chr1:178753614
|
T | A | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-23068T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178753614 | ||||||
| chr1:178753830
|
G | A | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-22852G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178753830 | ||||||
| chr1:178753841
|
T | C | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-83-22841T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178753841 | ||||||
| chr1:178753981
|
G | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(59): Show | 62 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.-83-22701G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178753981 | ||||||
| chr1:178753988
|
C | A | 15 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-83-22694C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178753988 | ||||||
| chr1:178753989
|
G | A | 1 | a0001c0001t0012g0040 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-83-22693G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178753989 | ||||||
| chr1:178754064
|
C | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-83-22618C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178754064 | ||||||
| chr1:178754065
|
G | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-83-22617G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178754065 | ||||||
| chr1:178754074
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-83-22608G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178754074 | ||||||
| chr1:178754076
|
C | G | 1 | a0001c0001t0001g0285 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-83-22606C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178754076 | ||||||
| chr1:178754196
|
A | G | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-83-22486A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178754196 | ||||||
| chr1:178754222
|
A | T | 15 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-83-22460A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178754222 | ||||||
| chr1:178754262
|
T | C | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-83-22420T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178754262 | ||||||
| chr1:178754416
|
A | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-22266A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178754416 | ||||||
| chr1:178754480
|
G | A | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-83-22202G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178754480 | ||||||
| chr1:178754553
|
T | G | 1 | a0001c0001t0001g0186 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-83-22129T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178754553 | ||||||
| chr1:178754575
|
A | G | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-83-22107A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178754575 | ||||||
| chr1:178754626
|
C | T | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-83-22056C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178754626 | ||||||
| chr1:178754817
|
T | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-21865T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178754817 | ||||||
| chr1:178754841
|
C | T | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-83-21841C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178754841 | ||||||
| chr1:178754874
|
A | G | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-83-21808A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178754874 | ||||||
| chr1:178754880
|
A | G | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-83-21802A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178754880 | ||||||
| chr1:178754934
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-83-21748G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178754934 | ||||||
| chr1:178754956
|
T | C | 2 | a0001c0001t0001g0215a0001c0001t0001g0285 | 2 | NA18967.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.-83-21726T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178754956 | ||||||
| chr1:178755008
|
C | G | 1 | a0001c0001t0008g0118 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-83-21674C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178755008 | ||||||
| chr1:178755088
|
A | C | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-83-21594A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178755088 | ||||||
| chr1:178755284
|
C | T | 44 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(41): Show | 44 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.-83-21398C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178755284 | ||||||
| chr1:178755300
|
A | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-21382A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178755300 | ||||||
| chr1:178755558
|
G | A | 137 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(134): Show | 137 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-83-21124G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178755558 | ||||||
| chr1:178755603
|
G | A | 1 | a0001c0001t0022g0059 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-83-21079G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178755603 | ||||||
| chr1:178755695
|
G | C | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-83-20987G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178755695 | ||||||
| chr1:178755757
|
G | A | 25 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(22): Show | 25 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-83-20925G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178755757 | ||||||
| chr1:178755776
|
A | G | 1 | a0001c0001t0027g0172 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-83-20906A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178755776 | ||||||
| chr1:178755940
|
G | A | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-83-20742G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178755940 | ||||||
| chr1:178756062
|
G | A | 25 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(22): Show | 25 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-83-20620G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178756062 | ||||||
| chr1:178756374
|
A | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-20308A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178756374 | ||||||
| chr1:178756385
|
G | A | 5 | a0001c0001t0002g0291a0001c0001t0002g0294a0001c0001t0002g0295others(2): Show | 5 | NA18939.hp1 NA18954.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-83-20297G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178756385 | ||||||
| chr1:178756392
|
C | G | 1 | a0001c0001t0001g0186 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-83-20290C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178756392 | ||||||
| chr1:178756660
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-83-20022A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178756660 | ||||||
| chr1:178756751
|
G | A | 305 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.-83-19931G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178756751 | ||||||
| chr1:178756754
|
G | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-83-19928G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178756754 | ||||||
| chr1:178756767
|
G | A | 35 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(32): Show | 35 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-83-19915G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178756767 | ||||||
| chr1:178757132
|
A | G | 1 | a0001c0001t0002g0107 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-83-19550A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178757132 | ||||||
| chr1:178757309
|
A | G | 2 | a0001c0001t0021g0075a0001c0001t0021g0076 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-83-19373A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178757309 | ||||||
| chr1:178757404
|
G | C | 2 | a0001c0001t0018g0080a0001c0001t0018g0096 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-83-19278G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178757404 | ||||||
| chr1:178757464
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-83-19218C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178757464 | ||||||
| chr1:178757510
|
G | C | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-83-19172G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178757510 | ||||||
| chr1:178757796
|
C | G | 7 | a0001c0001t0002g0082a0001c0001t0002g0094a0001c0001t0002g0095others(4): Show | 7 | NA18959.hp2 NA18966.hp1 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.-83-18886C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178757796 | ||||||
| chr1:178757923
|
T | G | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-83-18759T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178757923 | ||||||
| chr1:178758332
|
C | T | 1 | a0001c0002t0025g0149 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-83-18350C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178758332 | ||||||
| chr1:178758532
|
AC | A | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-83-18143delC | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178758532 | |||||
| chr1:178758734
|
G | A | 152 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(149): Show | 152 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-83-17948G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178758734 | ||||||
| chr1:178758810
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0002g0133 | 2 | HG01952.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.-83-17872G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178758810 | ||||||
| chr1:178758871
|
T | TG | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.-83-17809dupG | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178758871 | |||||
| chr1:178758896
|
T | C | 2 | a0001c0001t0021g0075a0001c0001t0021g0076 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-83-17786T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178758896 | ||||||
| chr1:178759054
|
C | T | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-83-17628C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178759054 | ||||||
| chr1:178759084
|
A | G | 1 | a0001c0001t0007g0072 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-83-17598A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178759084 | ||||||
| chr1:178759219
|
C | A | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-83-17463C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178759219 | ||||||
| chr1:178759483
|
A | G | 3 | a0001c0001t0001g0132a0001c0001t0002g0133a0001c0001t0035g0093 | 3 | HG01952.hp1 HG02129.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.-83-17199A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178759483 | ||||||
| chr1:178759527
|
C | CT | 10 | a0001c0001t0001g0056a0001c0001t0001g0216a0001c0001t0001g0283others(7): Show | 10 | HG00438.hp2 HG01168.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-83-17138dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178759527 | |||||
| chr1:178759527
|
CT | C | 84 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(81): Show | 84 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.-83-17138delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178759527 | |||||
| chr1:178759642
|
A | T | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-83-17040A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178759642 | ||||||
| chr1:178759687
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-83-16995A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178759687 | ||||||
| chr1:178759738
|
T | G | 6 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0145others(3): Show | 6 | HG00558.hp1 HG02040.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-16944T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178759738 | ||||||
| chr1:178760197
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-83-16485G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178760197 | ||||||
| chr1:178760204
|
AT | A | 3 | a0001c0001t0019g0146a0001c0001t0019g0147a0001c0001t0036g0137 | 3 | HG02486.hp2 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-83-16476delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178760204 | |||||
| chr1:178760228
|
A | C | 1 | a0001c0001t0001g0302 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-83-16454A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178760228 | ||||||
| chr1:178760347
|
T | G | 1 | a0001c0001t0001g0279 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-83-16335T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178760347 | ||||||
| chr1:178760485
|
A | G | 63 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(60): Show | 63 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.-83-16197A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178760485 | ||||||
| chr1:178760704
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-83-15978C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178760704 | ||||||
| chr1:178760739
|
C | G | 15 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-83-15943C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178760739 | ||||||
| chr1:178760768
|
GT | G | 15 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-83-15913delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178760768 | ||||||
| chr1:178760785
|
T | C | 9 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(6): Show | 9 | HG01069.hp1 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-83-15897T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178760785 | ||||||
| chr1:178760846
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-83-15836G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178760846 | ||||||
| chr1:178760938
|
C | T | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-83-15744C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178760938 | ||||||
| chr1:178760979
|
C | CT | 10 | a0001c0001t0001g0220a0001c0001t0001g0259a0001c0001t0009g0138others(7): Show | 10 | HG02055.hp2 HG02258.hp2 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.-83-15686dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178760979 | |||||
| chr1:178760979
|
CT | C | 7 | a0001c0001t0001g0174a0001c0001t0001g0238a0001c0001t0001g0304others(4): Show | 7 | HG01169.hp2 HG02280.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-83-15686delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178760979 | |||||
| chr1:178760983
|
T | A | 63 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(60): Show | 63 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.-83-15699T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178760983 | ||||||
| chr1:178761019
|
G | C | 1 | a0001c0001t0001g0298 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-83-15663G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761019 | ||||||
| chr1:178761172
|
G | A | 1 | a0001c0001t0009g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-83-15510G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761172 | ||||||
| chr1:178761191
|
G | A | 1 | a0001c0001t0006g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-83-15491G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761191 | ||||||
| chr1:178761229
|
G | A | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-83-15453G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761229 | ||||||
| chr1:178761313
|
C | G | 1 | a0001c0001t0001g0191 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-83-15369C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761313 | ||||||
| chr1:178761321
|
C | T | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-83-15361C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761321 | ||||||
| chr1:178761376
|
C | T | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-83-15306C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761376 | ||||||
| chr1:178761429
|
CA | C | 13 | a0001c0001t0006g0045a0001c0001t0006g0046a0001c0001t0006g0047others(10): Show | 13 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-83-15239delA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178761429 | |||||
| chr1:178761490
|
G | A | 15 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-83-15192G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761490 | ||||||
| chr1:178761551
|
G | A | 2 | a0001c0001t0001g0243a0001c0001t0001g0262 | 2 | NA18952.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.-83-15131G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761551 | ||||||
| chr1:178761560
|
T | C | 2 | a0001c0001t0019g0146a0001c0001t0019g0147 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-83-15122T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761560 | ||||||
| chr1:178761561
|
G | T | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-83-15121G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761561 | ||||||
| chr1:178761572
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0167 | 2 | HG00558.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-83-15110T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761572 | ||||||
| chr1:178761592
|
A | G | 152 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(149): Show | 152 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-83-15090A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761592 | ||||||
| chr1:178761670
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-83-15012C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761670 | ||||||
| chr1:178761722
|
G | A | 35 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(32): Show | 35 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-83-14960G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761722 | ||||||
| chr1:178761807
|
C | T | 11 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(8): Show | 11 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.-83-14875C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761807 | ||||||
| chr1:178761843
|
G | T | 1 | a0001c0002t0003g0031 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-83-14839G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761843 | ||||||
| chr1:178761891
|
C | T | 6 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-83-14791C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761891 | ||||||
| chr1:178761914
|
A | G | 6 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0104others(3): Show | 6 | NA18946.hp1 NA18993.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.-83-14768A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178761914 | ||||||
| chr1:178762086
|
A | G | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-83-14596A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178762086 | ||||||
| chr1:178762250
|
C | T | 1 | a0001c0002t0004g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-83-14432C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178762250 | ||||||
| chr1:178762340
|
G | A | 63 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(60): Show | 63 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.-83-14342G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178762340 | ||||||
| chr1:178762453
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0191 | 2 | NA18941.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.-83-14229C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178762453 | ||||||
| chr1:178762469
|
C | T | 11 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(8): Show | 11 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.-83-14213C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178762469 | ||||||
| chr1:178762511
|
G | A | 4 | a0001c0001t0013g0207a0001c0001t0013g0208a0001c0001t0013g0211others(1): Show | 4 | HG01106.hp1 HG01255.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.-83-14171G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178762511 | ||||||
| chr1:178762853
|
G | A | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-83-13829G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178762853 | ||||||
| chr1:178763178
|
T | C | 1 | a0001c0002t0025g0149 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-83-13504T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178763178 | ||||||
| chr1:178763319
|
C | T | 35 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(32): Show | 35 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-83-13363C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178763319 | ||||||
| chr1:178763452
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-83-13230A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178763452 | ||||||
| chr1:178763547
|
G | A | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-83-13135G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178763547 | ||||||
| chr1:178763874
|
G | T | 3 | a0001c0001t0001g0242a0001c0001t0001g0261a0001c0001t0001g0269 | 3 | HG00423.hp2 NA18947.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-83-12808G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178763874 | ||||||
| chr1:178763914
|
T | G | 1 | a0001c0001t0002g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-83-12768T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178763914 | ||||||
| chr1:178763920
|
G | A | 1 | a0001c0001t0006g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-83-12762G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178763920 | ||||||
| chr1:178764155
|
GGT | G | 202 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(199): Show | 202 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.-83-12520_-83-1251 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178764155 | |||||
| chr1:178764158
|
G | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-83-12524G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178764158 | ||||||
| chr1:178764473
|
A | G | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-83-12209A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178764473 | ||||||
| chr1:178764609
|
T | C | 1 | a0001c0002t0003g0026 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-83-12073T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178764609 | ||||||
| chr1:178764710
|
G | A | 1 | a0001c0001t0037g0077 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-83-11972G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178764710 | ||||||
| chr1:178764879
|
A | G | 2 | a0001c0001t0008g0112a0001c0001t0008g0114 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-83-11803A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178764879 | ||||||
| chr1:178765159
|
C | CT | 9 | a0001c0001t0001g0239a0001c0001t0001g0269a0001c0001t0001g0281others(6): Show | 9 | HG01069.hp1 HG01099.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-83-11509dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178765159 | |||||
| chr1:178765159
|
CTT | C | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-11510_-83-1150 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178765159 | |||||
| chr1:178765223
|
C | T | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-11459C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178765223 | ||||||
| chr1:178765243
|
A | G | 3 | a0001c0001t0001g0237a0001c0003t0017g0150a0001c0003t0017g0151 | 3 | HG01099.hp1 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-83-11439A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178765243 | ||||||
| chr1:178765281
|
C | T | 1 | a0001c0001t0016g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-83-11401C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178765281 | ||||||
| chr1:178765313
|
A | G | 1 | a0001c0001t0031g0231 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-83-11369A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178765313 | ||||||
| chr1:178765372
|
G | A | 1 | a0001c0002t0005g0008 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-83-11310G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178765372 | ||||||
| chr1:178765528
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-83-11154G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178765528 | ||||||
| chr1:178765553
|
A | C | 1 | a0001c0001t0001g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-83-11129A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178765553 | ||||||
| chr1:178765649
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0200 | 2 | HG02027.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.-83-11033C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178765649 | ||||||
| chr1:178765658
|
A | G | 1 | a0001c0001t0034g0293 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-83-11024A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178765658 | ||||||
| chr1:178765698
|
G | T | 1 | a0001c0001t0002g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-83-10984G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178765698 | ||||||
| chr1:178765830
|
T | G | 1 | a0001c0001t0037g0077 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-83-10852T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178765830 | ||||||
| chr1:178765943
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-83-10739G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178765943 | ||||||
| chr1:178765985
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-83-10697G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178765985 | ||||||
| chr1:178766129
|
A | G | 9 | a0001c0002t0004g0120a0001c0002t0004g0121a0001c0002t0004g0122others(6): Show | 9 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.-83-10553A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178766129 | ||||||
| chr1:178766386
|
A | AT | 6 | a0001c0001t0001g0285a0001c0001t0012g0039a0001c0001t0012g0040others(3): Show | 6 | HG00738.hp2 HG02698.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-10282dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178766386 | |||||
| chr1:178766386
|
AT | A | 129 | a0001c0001t0001g0132a0001c0001t0001g0215a0001c0001t0002g0002others(126): Show | 129 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.-83-10282delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178766386 | |||||
| chr1:178766467
|
G | C | 50 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(47): Show | 50 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.-83-10215G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178766467 | ||||||
| chr1:178766515
|
C | T | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-83-10167C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178766515 | ||||||
| chr1:178766526
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-83-10156G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178766526 | ||||||
| chr1:178766701
|
G | A | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-83-9981G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178766701 | ||||||
| chr1:178766738
|
T | A | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-83-9944T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178766738 | ||||||
| chr1:178766811
|
A | G | 1 | a0001c0001t0001g0263 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-83-9871A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178766811 | ||||||
| chr1:178766812
|
T | A | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-83-9870T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178766812 | ||||||
| chr1:178766850
|
C | T | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-9832C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178766850 | ||||||
| chr1:178767072
|
C | A | 1 | a0001c0001t0002g0136 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-83-9610C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178767072 | ||||||
| chr1:178767262
|
A | G | 2 | a0001c0001t0014g0267a0001c0001t0014g0268 | 2 | NA18747.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.-83-9420A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178767262 | ||||||
| chr1:178767358
|
C | CT | 48 | a0001c0001t0001g0052a0001c0001t0001g0159a0001c0001t0001g0175others(45): Show | 48 | HG00423.hp1 HG00544.hp1 HG01261.hp2 others(45): Show |
intron_variant | MODIFIER | c.-83-9301dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178767358 | |||||
| chr1:178767358
|
C | CTT | 8 | a0001c0001t0002g0295a0001c0001t0007g0071a0001c0001t0012g0039others(5): Show | 8 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.-83-9302_-83-9301d others(4): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178767358 | |||||
| chr1:178767358
|
CT | C | 41 | a0001c0001t0001g0051a0001c0001t0001g0055a0001c0001t0001g0160others(38): Show | 41 | HG00099.hp1 HG00733.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.-83-9301delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178767358 | |||||
| chr1:178767358
|
CTT | C | 10 | a0001c0001t0008g0113a0001c0001t0008g0119a0001c0001t0009g0138others(7): Show | 10 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-83-9302_-83-9301d others(4): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178767358 | |||||
| chr1:178767461
|
T | C | 35 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(32): Show | 35 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-83-9221T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178767461 | ||||||
| chr1:178767547
|
C | T | 63 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(60): Show | 63 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.-83-9135C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178767547 | ||||||
| chr1:178767671
|
G | C | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-9011G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178767671 | ||||||
| chr1:178767800
|
T | C | 10 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-83-8882T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178767800 | ||||||
| chr1:178767822
|
A | G | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-83-8860A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178767822 | ||||||
| chr1:178767901
|
G | A | 1 | a0001c0001t0009g0142 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-83-8781G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178767901 | ||||||
| chr1:178767943
|
A | G | 6 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-83-8739A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178767943 | ||||||
| chr1:178768122
|
T | C | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-83-8560T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178768122 | ||||||
| chr1:178768371
|
T | A | 1 | a0001c0001t0008g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-83-8311T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178768371 | ||||||
| chr1:178768405
|
G | A | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-83-8277G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178768405 | ||||||
| chr1:178768543
|
A | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-8139A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178768543 | ||||||
| chr1:178768730
|
C | T | 15 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0145others(12): Show | 15 | HG00558.hp1 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.-83-7952C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178768730 | ||||||
| chr1:178768848
|
T | C | 1 | a0001c0001t0001g0264 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-83-7834T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178768848 | ||||||
| chr1:178768850
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-83-7832G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178768850 | ||||||
| chr1:178768895
|
G | C | 1 | a0001c0001t0002g0133 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-83-7787G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178768895 | ||||||
| chr1:178769099
|
A | G | 3 | a0001c0001t0002g0089a0001c0001t0002g0100a0001c0001t0002g0136 | 3 | NA18974.hp1 NA19012.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-83-7583A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178769099 | ||||||
| chr1:178769449
|
A | T | 7 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0251others(4): Show | 7 | NA18951.hp2 NA18954.hp1 NA18974.hp2 others(4): Show |
intron_variant | MODIFIER | c.-83-7233A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178769449 | ||||||
| chr1:178769531
|
G | C | 1 | a0001c0001t0026g0271 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-83-7151G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178769531 | ||||||
| chr1:178769621
|
G | T | 1 | a0001c0001t0001g0191 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-83-7061G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178769621 | ||||||
| chr1:178769868
|
A | G | 1 | a0001c0001t0001g0274 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-83-6814A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178769868 | ||||||
| chr1:178769929
|
G | A | 37 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(34): Show | 37 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.-83-6753G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178769929 | ||||||
| chr1:178769955
|
G | A | 15 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-83-6727G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178769955 | ||||||
| chr1:178770018
|
CT | C | 123 | a0001c0001t0001g0213a0001c0001t0001g0281a0001c0001t0002g0002others(120): Show | 123 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.-83-6648delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178770018 | |||||
| chr1:178770018
|
CTT | C | 25 | a0001c0001t0002g0135a0001c0001t0006g0043a0001c0001t0006g0044others(22): Show | 25 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.-83-6649_-83-6648d others(4): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178770018 | |||||
| chr1:178770076
|
G | A | 15 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(12): Show | 15 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-83-6606G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178770076 | ||||||
| chr1:178770150
|
G | A | 25 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(22): Show | 25 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-83-6532G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178770150 | ||||||
| chr1:178770154
|
C | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0222 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-83-6528C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178770154 | ||||||
| chr1:178770194
|
T | C | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-83-6488T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178770194 | ||||||
| chr1:178770274
|
T | C | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.-83-6408T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178770274 | ||||||
| chr1:178770279
|
C | T | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-83-6403C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178770279 | ||||||
| chr1:178770315
|
T | C | 2 | a0001c0001t0001g0230a0001c0001t0001g0254 | 2 | NA19057.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-83-6367T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178770315 | ||||||
| chr1:178770422
|
A | G | 2 | a0001c0001t0002g0002a0001c0001t0002g0003 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-83-6260A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178770422 | ||||||
| chr1:178770485
|
A | G | 1 | a0001c0001t0001g0299 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-83-6197A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178770485 | ||||||
| chr1:178770507
|
CT | C | 25 | a0001c0001t0001g0173a0001c0001t0001g0218a0001c0001t0001g0264others(22): Show | 25 | HG01069.hp2 HG01074.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.-83-6156delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178770507 | |||||
| chr1:178770641
|
A | C | 1 | a0001c0001t0035g0093 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-83-6041A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178770641 | ||||||
| chr1:178770651
|
A | G | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.-83-6031A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178770651 | ||||||
| chr1:178770692
|
G | A | 1 | a0001c0002t0004g0120 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-83-5990G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178770692 | ||||||
| chr1:178770762
|
G | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-83-5920G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178770762 | ||||||
| chr1:178770764
|
A | G | 1 | a0001c0001t0016g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-83-5918A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178770764 | ||||||
| chr1:178770838
|
G | GT | 26 | a0001c0001t0001g0194a0001c0001t0001g0223a0001c0001t0001g0270others(23): Show | 26 | HG01192.hp1 HG01346.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.-83-5827dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178770838 | |||||
| chr1:178770930
|
G | A | 23 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.-83-5752G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178770930 | ||||||
| chr1:178770931
|
C | T | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.-83-5751C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178770931 | ||||||
| chr1:178770977
|
T | C | 5 | a0001c0001t0006g0046a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-83-5705T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178770977 | ||||||
| chr1:178770995
|
C | T | 43 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(40): Show | 43 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.-83-5687C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178770995 | ||||||
| chr1:178771059
|
G | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0222 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-83-5623G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178771059 | ||||||
| chr1:178771236
|
T | A | 2 | a0001c0001t0009g0138a0001c0001t0041g0139 | 2 | HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-83-5446T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178771236 | ||||||
| chr1:178771292
|
A | C | 203 | a0001c0001t0001g0056a0001c0001t0001g0132a0001c0001t0001g0155others(200): Show | 203 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.-83-5390A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178771292 | ||||||
| chr1:178771461
|
G | A | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-83-5221G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178771461 | ||||||
| chr1:178771574
|
A | AT | 33 | a0001c0001t0001g0222a0001c0001t0006g0043a0001c0001t0006g0044others(30): Show | 33 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-83-5099dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178771574 | |||||
| chr1:178771692
|
G | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-83-4990G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178771692 | ||||||
| chr1:178772001
|
G | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-83-4681G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178772001 | ||||||
| chr1:178772152
|
T | C | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-83-4530T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178772152 | ||||||
| chr1:178772197
|
A | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0259 | 2 | HG02293.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-83-4485A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178772197 | ||||||
| chr1:178772289
|
G | T | 1 | a0001c0001t0001g0232 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-83-4393G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178772289 | ||||||
| chr1:178772430
|
G | A | 57 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(54): Show | 57 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.-83-4252G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178772430 | ||||||
| chr1:178772446
|
A | G | 5 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-83-4236A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178772446 | ||||||
| chr1:178772762
|
A | C | 1 | a0001c0001t0001g0283 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-83-3920A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178772762 | ||||||
| chr1:178772795
|
A | G | 1 | a0001c0001t0006g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-83-3887A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178772795 | ||||||
| chr1:178773041
|
A | G | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-83-3641A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178773041 | ||||||
| chr1:178773084
|
G | A | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-83-3598G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178773084 | ||||||
| chr1:178773307
|
A | G | 289 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(286): Show | 289 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(286): Show |
intron_variant | MODIFIER | c.-83-3375A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178773307 | ||||||
| chr1:178773401
|
A | G | 46 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(43): Show | 46 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.-83-3281A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178773401 | ||||||
| chr1:178773432
|
A | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-3250A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178773432 | ||||||
| chr1:178773537
|
A | T | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-3145A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178773537 | ||||||
| chr1:178773545
|
T | A | 3 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045 | 3 | HG02886.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-83-3137T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178773545 | ||||||
| chr1:178773553
|
C | T | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-83-3129C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178773553 | ||||||
| chr1:178773620
|
C | T | 2 | a0001c0001t0002g0002a0001c0001t0002g0003 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-83-3062C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178773620 | ||||||
| chr1:178773706
|
G | C | 1 | a0001c0001t0002g0116 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-83-2976G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178773706 | ||||||
| chr1:178773769
|
C | G | 1 | a0001c0001t0026g0271 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-83-2913C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178773769 | ||||||
| chr1:178773770
|
T | A | 1 | a0001c0001t0026g0271 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-83-2912T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178773770 | ||||||
| chr1:178773774
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-83-2908C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178773774 | ||||||
| chr1:178773787
|
C | G | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-83-2895C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178773787 | ||||||
| chr1:178773795
|
C | CA | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-2873dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178773795 | |||||
| chr1:178773803
|
A | C | 1 | a0001c0001t0001g0157 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-83-2879A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178773803 | ||||||
| chr1:178773821
|
T | C | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-83-2861T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178773821 | ||||||
| chr1:178774052
|
C | T | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-2630C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178774052 | ||||||
| chr1:178774057
|
A | G | 6 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0104others(3): Show | 6 | NA18946.hp1 NA18993.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.-83-2625A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178774057 | ||||||
| chr1:178774060
|
G | A | 1 | a0001c0001t0001g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-83-2622G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178774060 | ||||||
| chr1:178774284
|
A | G | 50 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(47): Show | 50 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.-83-2398A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178774284 | ||||||
| chr1:178774472
|
T | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-83-2210T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178774472 | ||||||
| chr1:178774514
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-83-2168G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178774514 | ||||||
| chr1:178774599
|
C | T | 10 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-83-2083C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178774599 | ||||||
| chr1:178774702
|
T | A | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-83-1980T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178774702 | ||||||
| chr1:178774707
|
C | T | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-83-1975C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178774707 | ||||||
| chr1:178774898
|
C | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0222 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-83-1784C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178774898 | ||||||
| chr1:178775116
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-83-1566A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178775116 | ||||||
| chr1:178775129
|
C | T | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-83-1553C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178775129 | ||||||
| chr1:178775170
|
C | T | 2 | a0001c0001t0015g0108a0001c0001t0015g0109 | 2 | HG00280.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.-83-1512C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178775170 | ||||||
| chr1:178775192
|
A | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0216 | 2 | HG02135.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-83-1490A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178775192 | ||||||
| chr1:178775249
|
T | G | 1 | a0001c0001t0001g0165 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-83-1433T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178775249 | ||||||
| chr1:178775353
|
A | G | 1 | a0001c0001t0001g0305 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-83-1329A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178775353 | ||||||
| chr1:178775589
|
T | A | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-83-1093T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178775589 | ||||||
| chr1:178775630
|
T | C | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-83-1052T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178775630 | ||||||
| chr1:178775690
|
A | G | 2 | a0001c0002t0004g0126a0001c0002t0024g0123 | 2 | HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-83-992A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178775690 | ||||||
| chr1:178775740
|
A | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-83-942A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178775740 | ||||||
| chr1:178775920
|
C | CA | 11 | a0001c0001t0001g0250a0001c0001t0001g0285a0001c0001t0006g0048others(8): Show | 11 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.-83-746dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178775920 | |||||
| chr1:178776003
|
A | G | 9 | a0001c0001t0001g0162a0001c0001t0001g0173a0001c0001t0001g0181others(6): Show | 9 | HG00597.hp1 HG02027.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.-83-679A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178776003 | ||||||
| chr1:178776018
|
G | A | 73 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(70): Show | 73 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.-83-664G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178776018 | ||||||
| chr1:178776055
|
G | A | 2 | a0001c0001t0019g0146a0001c0001t0019g0147 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-83-627G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178776055 | ||||||
| chr1:178776090
|
G | C | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-83-592G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178776090 | ||||||
| chr1:178776290
|
T | G | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-83-392T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178776290 | ||||||
| chr1:178776476
|
A | T | 46 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(43): Show | 46 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.-83-206A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178776476 | ||||||
| chr1:178776566
|
T | A | 1 | a0001c0001t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-83-116T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178776566 | ||||||
| chr1:178776588
|
T | C | 3 | a0001c0001t0014g0267a0001c0001t0014g0268a0001c0001t0014g0275 | 3 | HG00544.hp2 NA18747.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.-83-94T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178776588 | ||||||
| chr1:178776663
|
CT | C | 167 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(164): Show | 167 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(164): Show |
splice_region_variant&intron_variant | LOW | c.-83-5delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178776663 | |||||
| chr1:178776663
|
CTT | C | 35 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(32): Show | 35 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(32): Show |
splice_region_variant&intron_variant | LOW | c.-83-6_-83-5delTT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr1 | 178776663 | |||||
| chr1:178776896
|
C | T | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.57+75C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178776896 | ||||||
| chr1:178776944
|
T | C | 2 | a0001c0002t0023g0005a0001c0002t0023g0006 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.57+123T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178776944 | ||||||
| chr1:178776966
|
T | TA | 7 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0027others(4): Show | 7 | HG00544.hp1 NA18962.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+146dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr1 | 178776966 | |||||
| chr1:178776986
|
A | G | 37 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(34): Show | 37 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.57+165A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178776986 | ||||||
| chr1:178777040
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.57+219C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178777040 | ||||||
| chr1:178777085
|
A | G | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.57+264A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178777085 | ||||||
| chr1:178777102
|
T | C | 1 | a0001c0001t0011g0240 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.57+281T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178777102 | ||||||
| chr1:178777117
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.57+296A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178777117 | ||||||
| chr1:178777282
|
C | A | 1 | a0001c0001t0002g0110 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.57+461C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178777282 | ||||||
| chr1:178777381
|
G | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0212a0001c0001t0001g0222 | 3 | HG02970.hp2 NA18906.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.57+560G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178777381 | ||||||
| chr1:178777423
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.57+602C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178777423 | ||||||
| chr1:178777447
|
G | C | 2 | a0001c0001t0001g0160a0001c0001t0001g0206 | 2 | NA18962.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.57+626G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178777447 | ||||||
| chr1:178777510
|
A | G | 9 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(6): Show | 9 | HG01069.hp1 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+689A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178777510 | ||||||
| chr1:178777652
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.57+831G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178777652 | ||||||
| chr1:178777779
|
A | T | 1 | a0001c0002t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.57+958A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178777779 | ||||||
| chr1:178777787
|
C | T | 2 | a0001c0001t0022g0059a0001c0002t0004g0012 | 2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.57+966C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178777787 | ||||||
| chr1:178777880
|
A | C | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.57+1059A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178777880 | ||||||
| chr1:178777900
|
G | C | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.57+1079G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178777900 | ||||||
| chr1:178777915
|
C | T | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.57+1094C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178777915 | ||||||
| chr1:178777932
|
T | G | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.57+1111T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178777932 | ||||||
| chr1:178778028
|
A | C | 1 | a0001c0001t0011g0257 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.57+1207A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778028 | ||||||
| chr1:178778131
|
C | T | 13 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.57+1310C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778131 | ||||||
| chr1:178778132
|
A | G | 82 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(79): Show | 82 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.57+1311A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778132 | ||||||
| chr1:178778154
|
T | G | 3 | a0001c0002t0003g0015a0001c0002t0023g0005a0001c0002t0023g0006 | 3 | HG02922.hp2 HG03516.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.57+1333T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778154 | ||||||
| chr1:178778197
|
G | T | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.57+1376G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778197 | ||||||
| chr1:178778283
|
A | T | 1 | a0001c0002t0024g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.57+1462A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778283 | ||||||
| chr1:178778303
|
T | C | 2 | a0001c0001t0018g0080a0001c0001t0018g0096 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.57+1482T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778303 | ||||||
| chr1:178778310
|
G | C | 305 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.57+1489G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778310 | ||||||
| chr1:178778336
|
A | G | 1 | a0001c0002t0005g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.57+1515A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778336 | ||||||
| chr1:178778393
|
A | G | 13 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(10): Show | 13 | HG00738.hp2 HG01884.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.57+1572A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778393 | ||||||
| chr1:178778429
|
C | G | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+1608C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778429 | ||||||
| chr1:178778487
|
G | A | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+1666G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778487 | ||||||
| chr1:178778513
|
A | T | 1 | a0001c0004t0004g0001 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.57+1692A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778513 | ||||||
| chr1:178778557
|
G | T | 3 | a0001c0001t0001g0250a0001c0001t0020g0004a0001c0001t0020g0038 | 3 | HG02622.hp2 HG02717.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.57+1736G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778557 | ||||||
| chr1:178778594
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.57+1773C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778594 | ||||||
| chr1:178778600
|
T | G | 1 | a0001c0001t0001g0250 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.57+1779T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778600 | ||||||
| chr1:178778617
|
C | T | 3 | a0001c0001t0002g0084a0001c0001t0002g0087a0001c0001t0002g0103 | 3 | NA18995.hp1 NA19009.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.57+1796C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778617 | ||||||
| chr1:178778688
|
T | G | 1 | a0001c0001t0033g0202 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.57+1867T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778688 | ||||||
| chr1:178778692
|
C | T | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+1871C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778692 | ||||||
| chr1:178778715
|
T | TA | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+1900dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr1 | 178778715 | |||||
| chr1:178778753
|
A | T | 1 | a0001c0001t0011g0240 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.57+1932A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778753 | ||||||
| chr1:178779042
|
T | C | 2 | a0001c0002t0003g0018a0001c0002t0003g0019 | 2 | NA19060.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.57+2221T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178779042 | ||||||
| chr1:178779207
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.57+2386G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178779207 | ||||||
| chr1:178779401
|
A | G | 1 | a0001c0001t0001g0237 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.57+2580A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178779401 | ||||||
| chr1:178779426
|
A | T | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.57+2605A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178779426 | ||||||
| chr1:178779698
|
A | G | 1 | a0001c0001t0016g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.57+2877A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178779698 | ||||||
| chr1:178779738
|
T | C | 2 | a0001c0002t0004g0012a0001c0002t0004g0129 | 2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.57+2917T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178779738 | ||||||
| chr1:178779772
|
T | C | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.57+2951T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178779772 | ||||||
| chr1:178780119
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.57+3298T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178780119 | ||||||
| chr1:178780260
|
A | G | 7 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(4): Show | 7 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+3439A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178780260 | ||||||
| chr1:178780262
|
C | T | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.57+3441C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178780262 | ||||||
| chr1:178780704
|
A | G | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.58-3714A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178780704 | ||||||
| chr1:178780848
|
TCCTATTT others(3): Show |
T | 1 | a0001c0001t0002g0290 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.58-3569_58-3560del others(10): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178780848 | ||||||
| chr1:178781012
|
T | TTA | 7 | a0001c0001t0001g0229a0001c0001t0001g0235a0001c0001t0001g0236others(4): Show | 7 | HG01099.hp1 HG01243.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.58-3392_58-3391dup others(2): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr1 | 178781012 | |||||
| chr1:178781122
|
C | A | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.58-3296C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178781122 | ||||||
| chr1:178781133
|
A | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-3285A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178781133 | ||||||
| chr1:178781389
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.58-3029G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178781389 | ||||||
| chr1:178781492
|
A | G | 46 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(43): Show | 46 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.58-2926A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178781492 | ||||||
| chr1:178781631
|
C | A | 1 | a0001c0002t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.58-2787C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178781631 | ||||||
| chr1:178781812
|
A | G | 1 | a0001c0001t0019g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.58-2606A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178781812 | ||||||
| chr1:178782010
|
C | T | 1 | a0001c0002t0024g0123 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.58-2408C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178782010 | ||||||
| chr1:178782096
|
A | G | 62 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(59): Show | 62 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.58-2322A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178782096 | ||||||
| chr1:178782349
|
C | T | 5 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(2): Show | 5 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-2069C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178782349 | ||||||
| chr1:178782462
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.58-1956A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178782462 | ||||||
| chr1:178782523
|
C | T | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-1895C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178782523 | ||||||
| chr1:178782647
|
A | C | 151 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(148): Show | 151 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.58-1771A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178782647 | ||||||
| chr1:178783000
|
A | G | 70 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0057others(67): Show | 70 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.58-1418A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178783000 | ||||||
| chr1:178783096
|
A | C | 1 | a0001c0001t0001g0252 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.58-1322A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178783096 | ||||||
| chr1:178783103
|
A | G | 1 | a0001c0001t0035g0093 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.58-1315A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178783103 | ||||||
| chr1:178783208
|
G | A | 9 | a0001c0001t0001g0154a0001c0001t0006g0043a0001c0001t0006g0044others(6): Show | 9 | HG00280.hp1 HG01884.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.58-1210G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178783208 | ||||||
| chr1:178783248
|
G | C | 35 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(32): Show | 35 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.58-1170G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178783248 | ||||||
| chr1:178783615
|
G | T | 1 | a0001c0001t0001g0170 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.58-803G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178783615 | ||||||
| chr1:178783627
|
C | T | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.58-791C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178783627 | ||||||
| chr1:178783777
|
C | A | 1 | a0001c0001t0002g0306 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.58-641C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178783777 | ||||||
| chr1:178783815
|
G | A | 44 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(41): Show | 44 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.58-603G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178783815 | ||||||
| chr1:178783848
|
C | T | 2 | a0001c0001t0001g0228a0001c0001t0001g0234 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.58-570C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178783848 | ||||||
| chr1:178783850
|
A | G | 151 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(148): Show | 151 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.58-568A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178783850 | ||||||
| chr1:178784027
|
G | A | 151 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(148): Show | 151 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.58-391G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178784027 | ||||||
| chr1:178784143
|
T | G | 46 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(43): Show | 46 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.58-275T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178784143 | ||||||
| chr1:178784261
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.58-157C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178784261 | ||||||
| chr1:178784285
|
A | G | 2 | a0001c0001t0021g0075a0001c0001t0021g0076 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.58-133A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178784285 | ||||||
| chr1:178784393
|
G | C | 2 | a0001c0002t0005g0036a0001c0002t0005g0037 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.58-25G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178784393 | ||||||
| chr1:178784858
|
G | T | 11 | a0001c0001t0001g0162a0001c0001t0001g0173a0001c0001t0001g0181others(8): Show | 11 | HG00597.hp1 HG01123.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+336G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 3/19 | chr1 | 178784858 | ||||||
| chr1:178784865
|
T | A | 1 | a0001c0001t0006g0044 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.162+343T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 3/19 | chr1 | 178784865 | ||||||
| chr1:178785095
|
A | G | 2 | a0001c0001t0019g0146a0001c0001t0019g0147 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.163-462A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 3/19 | chr1 | 178785095 | ||||||
| chr1:178785523
|
A | C | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.163-34A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 3/19 | chr1 | 178785523 | ||||||
| chr1:178785789
|
G | A | 5 | a0001c0001t0001g0162a0001c0001t0001g0181a0001c0001t0001g0182others(2): Show | 5 | HG00597.hp1 NA18966.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+182G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178785789 | ||||||
| chr1:178785839
|
G | A | 1 | a0001c0001t0006g0044 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.213+232G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178785839 | ||||||
| chr1:178785878
|
T | G | 1 | a0001c0002t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.213+271T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178785878 | ||||||
| chr1:178785879
|
T | C | 1 | a0001c0002t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.213+272T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178785879 | ||||||
| chr1:178785899
|
T | A | 1 | a0001c0001t0002g0290 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.213+292T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178785899 | ||||||
| chr1:178786024
|
A | G | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.213+417A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786024 | ||||||
| chr1:178786068
|
G | A | 1 | a0001c0001t0002g0290 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.213+461G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786068 | ||||||
| chr1:178786069
|
G | C | 1 | a0001c0001t0002g0290 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.213+462G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786069 | ||||||
| chr1:178786072
|
G | A | 1 | a0001c0001t0008g0118 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.213+465G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786072 | ||||||
| chr1:178786072
|
G | C | 1 | a0001c0001t0002g0290 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.213+465G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786072 | ||||||
| chr1:178786073
|
C | T | 1 | a0001c0001t0002g0290 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.213+466C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786073 | ||||||
| chr1:178786074
|
G | A | 2 | a0001c0001t0002g0290a0001c0002t0005g0007 | 2 | HG00099.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.213+467G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786074 | ||||||
| chr1:178786079
|
A | T | 1 | a0001c0001t0002g0290 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.213+472A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786079 | ||||||
| chr1:178786080
|
T | G | 1 | a0001c0001t0002g0290 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.213+473T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786080 | ||||||
| chr1:178786081
|
C | T | 1 | a0001c0001t0002g0290 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.213+474C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786081 | ||||||
| chr1:178786082
|
A | T | 1 | a0001c0001t0002g0290 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.213+475A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786082 | ||||||
| chr1:178786180
|
C | T | 1 | a0001c0001t0006g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.213+573C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786180 | ||||||
| chr1:178786250
|
A | G | 1 | a0001c0002t0004g0120 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.213+643A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786250 | ||||||
| chr1:178786289
|
A | G | 1 | a0001c0001t0002g0133 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.213+682A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786289 | ||||||
| chr1:178786297
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.213+690A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786297 | ||||||
| chr1:178786347
|
A | T | 1 | a0001c0001t0010g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.213+740A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786347 | ||||||
| chr1:178786428
|
G | A | 1 | a0001c0001t0007g0066 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.213+821G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786428 | ||||||
| chr1:178786487
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.213+880G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786487 | ||||||
| chr1:178786493
|
A | G | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.213+886A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786493 | ||||||
| chr1:178786555
|
A | G | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.213+948A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786555 | ||||||
| chr1:178786563
|
A | G | 1 | a0001c0001t0031g0231 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.213+956A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178786563 | ||||||
| chr1:178787089
|
A | G | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.213+1482A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178787089 | ||||||
| chr1:178787101
|
A | T | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.213+1494A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178787101 | ||||||
| chr1:178787187
|
A | T | 1 | a0001c0001t0001g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.213+1580A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178787187 | ||||||
| chr1:178787221
|
C | G | 1 | a0001c0001t0002g0133 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.213+1614C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178787221 | ||||||
| chr1:178787285
|
T | C | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+1678T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178787285 | ||||||
| chr1:178787420
|
G | A | 58 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(55): Show | 58 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.213+1813G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178787420 | ||||||
| chr1:178787634
|
A | T | 151 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(148): Show | 151 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.213+2027A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178787634 | ||||||
| chr1:178787785
|
C | A | 1 | a0001c0001t0010g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.213+2178C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178787785 | ||||||
| chr1:178787870
|
A | G | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+2263A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178787870 | ||||||
| chr1:178787887
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.213+2280G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178787887 | ||||||
| chr1:178787921
|
C | A | 1 | a0001c0001t0006g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.213+2314C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178787921 | ||||||
| chr1:178787991
|
T | G | 1 | a0001c0001t0001g0249 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.213+2384T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178787991 | ||||||
| chr1:178788047
|
A | G | 1 | a0001c0001t0001g0215 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.213+2440A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178788047 | ||||||
| chr1:178788103
|
T | A | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.213+2496T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178788103 | ||||||
| chr1:178788241
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.213+2634G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178788241 | ||||||
| chr1:178788272
|
T | G | 46 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(43): Show | 46 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.213+2665T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178788272 | ||||||
| chr1:178788353
|
A | C | 5 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+2746A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178788353 | ||||||
| chr1:178788458
|
G | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+2851G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178788458 | ||||||
| chr1:178788497
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.213+2890A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178788497 | ||||||
| chr1:178788608
|
G | A | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.213+3001G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178788608 | ||||||
| chr1:178788617
|
G | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+3010G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178788617 | ||||||
| chr1:178788756
|
G | A | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+3149G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178788756 | ||||||
| chr1:178788758
|
G | A | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.213+3151G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178788758 | ||||||
| chr1:178788804
|
C | CTTTCT | 12 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(9): Show | 12 | HG01884.hp1 HG02280.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.213+3216_213+3220d others(7): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178788804 | |||||
| chr1:178788821
|
TTC | T | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.213+3216_213+3217d others(4): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178788821 | |||||
| chr1:178788828
|
G | C | 3 | a0001c0001t0001g0158a0001c0001t0006g0047a0001c0001t0036g0137 | 3 | HG02723.hp1 HG02970.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.213+3221G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178788828 | ||||||
| chr1:178788829
|
T | TTTTC | 39 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0160others(36): Show | 39 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.213+3238_213+3241d others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178788829 | |||||
| chr1:178788833
|
C | T | 2 | a0001c0001t0006g0047a0001c0001t0036g0137 | 2 | HG02723.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.213+3226C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178788833 | ||||||
| chr1:178788833
|
CTTTCTTT others(6): Show |
C | 1 | a0001c0003t0017g0151 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.213+3234_213+3246d others(15): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178788833 | |||||
| chr1:178788837
|
CTTTCTTT others(7): Show |
C | 1 | a0001c0001t0002g0131 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.213+3238_213+3251d others(16): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178788837 | |||||
| chr1:178788837
|
CTTTCTTT others(12): Show |
C | 1 | a0001c0001t0002g0083 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.213+3238_213+3256d others(21): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178788837 | |||||
| chr1:178788841
|
C | CTTTCT | 9 | a0001c0001t0001g0055a0001c0001t0001g0185a0001c0001t0001g0229others(6): Show | 9 | HG00438.hp1 HG01257.hp2 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.213+3272_213+3276d others(7): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178788841 | |||||
| chr1:178788841
|
C | CTTTCTTT others(2): Show |
8 | a0001c0001t0001g0173a0001c0001t0001g0195a0001c0001t0001g0220others(5): Show | 8 | HG01106.hp2 HG01256.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+3241_213+3242i others(11): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178788841 | |||||
| chr1:178788841
|
C | CTTTCTTT others(7): Show |
2 | a0001c0001t0006g0048a0001c0001t0006g0049 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.213+3241_213+3242i others(16): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178788841 | |||||
| chr1:178788841
|
C | CTTTCTTT others(32): Show |
2 | a0001c0001t0021g0075a0001c0001t0021g0076 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.213+3241_213+3242i others(41): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178788841 | |||||
| chr1:178788841
|
C | CTTTCTTT others(3): Show |
3 | a0001c0001t0001g0258a0001c0001t0006g0043a0001c0001t0006g0044 | 3 | HG01243.hp2 HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.213+3267_213+3276d others(12): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178788841 | |||||
| chr1:178788841
|
C | CTTTCTTT others(13): Show |
1 | a0001c0001t0006g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.213+3257_213+3276d others(22): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178788841 | |||||
| chr1:178788841
|
C | CTTTTCTT others(9): Show |
2 | a0001c0002t0023g0005a0001c0002t0023g0006 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.213+3237_213+3238i others(18): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178788841 | |||||
| chr1:178788841
|
CTTTCT | C | 22 | a0001c0001t0001g0225a0001c0001t0001g0246a0001c0001t0001g0247others(19): Show | 22 | HG00099.hp1 HG00280.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.213+3272_213+3276d others(7): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178788841 | |||||
| chr1:178788841
|
CTTTCTTT others(3): Show |
C | 114 | a0001c0001t0001g0132a0001c0001t0001g0219a0001c0001t0001g0224others(111): Show | 114 | HG00423.hp1 HG00544.hp1 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.213+3267_213+3276d others(12): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178788841 | |||||
| chr1:178788841
|
CTTTCTTT others(8): Show |
C | 8 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+3262_213+3276d others(17): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178788841 | |||||
| chr1:178788845
|
CT | C | 3 | a0001c0001t0001g0166a0001c0001t0001g0182a0001c0001t0006g0047 | 3 | HG02723.hp1 HG03704.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.213+3242delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178788845 | |||||
| chr1:178788851
|
T | C | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.213+3244T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178788851 | ||||||
| chr1:178788985
|
CA | C | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+3380delA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178788985 | |||||
| chr1:178788988
|
C | T | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+3381C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178788988 | ||||||
| chr1:178788989
|
C | T | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+3382C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178788989 | ||||||
| chr1:178789019
|
A | C | 44 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(41): Show | 44 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.213+3412A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178789019 | ||||||
| chr1:178789020
|
C | T | 1 | a0001c0001t0010g0062 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.213+3413C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178789020 | ||||||
| chr1:178789072
|
A | G | 5 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+3465A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178789072 | ||||||
| chr1:178789091
|
C | G | 63 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(60): Show | 63 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.213+3484C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178789091 | ||||||
| chr1:178789222
|
A | G | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+3615A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178789222 | ||||||
| chr1:178789230
|
G | A | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.213+3623G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178789230 | ||||||
| chr1:178789434
|
T | C | 1 | a0001c0001t0027g0172 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.213+3827T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178789434 | ||||||
| chr1:178789464
|
C | T | 5 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.213+3857C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178789464 | ||||||
| chr1:178789534
|
G | A | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.213+3927G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178789534 | ||||||
| chr1:178789633
|
A | G | 1 | a0001c0002t0005g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.213+4026A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178789633 | ||||||
| chr1:178790024
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.213+4417C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178790024 | ||||||
| chr1:178790042
|
A | G | 46 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(43): Show | 46 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.213+4435A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178790042 | ||||||
| chr1:178790114
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.213+4507A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178790114 | ||||||
| chr1:178790200
|
C | T | 11 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0145others(8): Show | 11 | HG00558.hp1 HG01243.hp2 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.213+4593C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178790200 | ||||||
| chr1:178790243
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.213+4636G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178790243 | ||||||
| chr1:178790311
|
A | G | 7 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(4): Show | 7 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.213+4704A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178790311 | ||||||
| chr1:178790510
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.213+4903T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178790510 | ||||||
| chr1:178790910
|
C | T | 1 | a0001c0001t0008g0118 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.213+5303C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178790910 | ||||||
| chr1:178790923
|
A | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.213+5316A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178790923 | ||||||
| chr1:178790993
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.213+5386A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178790993 | ||||||
| chr1:178791049
|
C | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0222 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.213+5442C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178791049 | ||||||
| chr1:178791266
|
A | G | 5 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(2): Show | 5 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.213+5659A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178791266 | ||||||
| chr1:178791287
|
A | AT | 100 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0157others(97): Show | 100 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.213+5700dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178791287 | |||||
| chr1:178791326
|
A | T | 1 | a0001c0001t0002g0133 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.213+5719A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178791326 | ||||||
| chr1:178791357
|
G | A | 1 | a0001c0002t0004g0121 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.213+5750G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178791357 | ||||||
| chr1:178791540
|
C | G | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.213+5933C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178791540 | ||||||
| chr1:178791612
|
A | G | 1 | a0001c0001t0002g0153 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.213+6005A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178791612 | ||||||
| chr1:178791619
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.213+6012A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178791619 | ||||||
| chr1:178791658
|
C | G | 1 | a0001c0002t0016g0030 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.213+6051C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178791658 | ||||||
| chr1:178791728
|
G | A | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+6121G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178791728 | ||||||
| chr1:178791737
|
A | G | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+6130A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178791737 | ||||||
| chr1:178791884
|
C | T | 1 | a0001c0001t0002g0095 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.213+6277C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178791884 | ||||||
| chr1:178791885
|
G | A | 3 | a0001c0001t0002g0082a0001c0001t0002g0094a0001c0001t0002g0287 | 3 | NA18966.hp1 NA18968.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.213+6278G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178791885 | ||||||
| chr1:178792143
|
G | A | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.213+6536G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178792143 | ||||||
| chr1:178792244
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.213+6637T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178792244 | ||||||
| chr1:178792264
|
G | C | 2 | a0001c0001t0001g0246a0001c0001t0001g0273 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.213+6657G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178792264 | ||||||
| chr1:178792680
|
G | T | 44 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(41): Show | 44 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.213+7073G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178792680 | ||||||
| chr1:178792687
|
C | G | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+7080C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178792687 | ||||||
| chr1:178792691
|
G | T | 44 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(41): Show | 44 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.213+7084G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178792691 | ||||||
| chr1:178792704
|
G | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.213+7097G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178792704 | ||||||
| chr1:178792803
|
C | T | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.213+7196C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178792803 | ||||||
| chr1:178792856
|
G | A | 17 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(14): Show | 17 | HG01884.hp1 HG02055.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.213+7249G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178792856 | ||||||
| chr1:178792936
|
C | T | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.213+7329C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178792936 | ||||||
| chr1:178792974
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.213+7367A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178792974 | ||||||
| chr1:178793115
|
A | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.213+7508A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178793115 | ||||||
| chr1:178793133
|
G | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0191 | 2 | NA18941.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.213+7526G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178793133 | ||||||
| chr1:178793167
|
G | A | 1 | a0001c0002t0003g0023 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.213+7560G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178793167 | ||||||
| chr1:178793263
|
G | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0255a0001c0001t0001g0304 | 3 | HG01123.hp1 HG01169.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.213+7656G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178793263 | ||||||
| chr1:178793401
|
C | CT | 13 | a0001c0001t0001g0216a0001c0001t0001g0251a0001c0001t0001g0266others(10): Show | 13 | HG00741.hp2 HG01099.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.213+7814dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178793401 | |||||
| chr1:178793401
|
CT | C | 19 | a0001c0001t0001g0054a0001c0001t0001g0158a0001c0001t0001g0164others(16): Show | 19 | HG01069.hp1 HG01070.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.213+7814delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178793401 | |||||
| chr1:178793436
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.213+7829C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178793436 | ||||||
| chr1:178793437
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.213+7830G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178793437 | ||||||
| chr1:178793453
|
T | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.213+7846T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178793453 | ||||||
| chr1:178793796
|
G | A | 287 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0056others(284): Show | 287 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.213+8189G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178793796 | ||||||
| chr1:178793800
|
T | C | 1 | a0002c0005t0039g0042 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.213+8193T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178793800 | ||||||
| chr1:178793870
|
T | C | 2 | a0001c0001t0019g0146a0001c0001t0019g0147 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.213+8263T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178793870 | ||||||
| chr1:178793926
|
A | G | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.213+8319A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178793926 | ||||||
| chr1:178793934
|
T | A | 62 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(59): Show | 62 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.213+8327T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178793934 | ||||||
| chr1:178794027
|
T | C | 1 | a0001c0002t0004g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.213+8420T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178794027 | ||||||
| chr1:178794058
|
C | T | 4 | a0001c0001t0001g0229a0001c0001t0001g0235a0001c0001t0001g0236others(1): Show | 4 | HG01243.hp2 HG01257.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.213+8451C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178794058 | ||||||
| chr1:178794233
|
C | T | 1 | a0001c0002t0005g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.213+8626C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178794233 | ||||||
| chr1:178794334
|
G | T | 76 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(73): Show | 76 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.213+8727G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178794334 | ||||||
| chr1:178794391
|
G | A | 1 | a0001c0001t0006g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.213+8784G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178794391 | ||||||
| chr1:178794671
|
A | G | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.213+9064A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178794671 | ||||||
| chr1:178794727
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.213+9120A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178794727 | ||||||
| chr1:178795018
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.213+9411A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178795018 | ||||||
| chr1:178795039
|
G | A | 9 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(6): Show | 9 | HG01069.hp1 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.213+9432G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178795039 | ||||||
| chr1:178795102
|
C | T | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.213+9495C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178795102 | ||||||
| chr1:178795179
|
C | CA | 25 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.213+9584dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178795179 | |||||
| chr1:178795276
|
T | C | 4 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0178others(1): Show | 4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+9669T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178795276 | ||||||
| chr1:178795760
|
C | T | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.213+10153C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178795760 | ||||||
| chr1:178795803
|
T | C | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.213+10196T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178795803 | ||||||
| chr1:178795895
|
G | A | 1 | a0001c0001t0034g0293 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.213+10288G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178795895 | ||||||
| chr1:178795987
|
C | T | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.213+10380C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178795987 | ||||||
| chr1:178796013
|
T | G | 42 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(39): Show | 42 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.213+10406T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178796013 | ||||||
| chr1:178796889
|
A | G | 2 | a0001c0001t0002g0002a0001c0001t0002g0003 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.214-11156A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178796889 | ||||||
| chr1:178796919
|
A | T | 1 | a0001c0001t0006g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.214-11126A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178796919 | ||||||
| chr1:178796932
|
T | C | 1 | a0001c0001t0008g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.214-11113T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178796932 | ||||||
| chr1:178796955
|
C | T | 2 | a0001c0002t0005g0036a0001c0002t0005g0037 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.214-11090C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178796955 | ||||||
| chr1:178797175
|
T | A | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.214-10870T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178797175 | ||||||
| chr1:178797343
|
A | C | 3 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045 | 3 | HG02886.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.214-10702A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178797343 | ||||||
| chr1:178797344
|
G | C | 3 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045 | 3 | HG02886.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.214-10701G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178797344 | ||||||
| chr1:178797490
|
T | C | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.214-10555T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178797490 | ||||||
| chr1:178797524
|
A | G | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-10521A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178797524 | ||||||
| chr1:178797617
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.214-10428C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178797617 | ||||||
| chr1:178797652
|
C | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.214-10393C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178797652 | ||||||
| chr1:178797656
|
C | A | 1 | a0002c0005t0039g0042 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.214-10389C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178797656 | ||||||
| chr1:178797657
|
A | G | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.214-10388A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178797657 | ||||||
| chr1:178797686
|
A | G | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.214-10359A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178797686 | ||||||
| chr1:178797718
|
A | T | 19 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(16): Show | 19 | HG01099.hp1 HG01884.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.214-10327A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178797718 | ||||||
| chr1:178797759
|
A | G | 51 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(48): Show | 51 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.214-10286A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178797759 | ||||||
| chr1:178797813
|
A | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-10232A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178797813 | ||||||
| chr1:178797985
|
T | TA | 70 | a0001c0001t0001g0055a0001c0001t0001g0132a0001c0001t0001g0145others(67): Show | 70 | HG00280.hp2 HG00558.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.214-10040dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178797985 | |||||
| chr1:178797985
|
T | TAA | 30 | a0001c0001t0002g0003a0001c0001t0002g0078a0001c0001t0002g0092others(27): Show | 30 | HG00738.hp2 HG01346.hp2 HG01361.hp2 others(27): Show |
intron_variant | MODIFIER | c.214-10041_214-1004 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178797985 | |||||
| chr1:178797985
|
T | TAAA | 10 | a0001c0001t0007g0066a0001c0001t0009g0144a0001c0001t0010g0074others(7): Show | 10 | HG01099.hp1 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.214-10042_214-1004 others(7): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178797985 | |||||
| chr1:178797985
|
T | TAAAA | 27 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(24): Show | 27 | HG00544.hp1 HG00642.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.214-10043_214-1004 others(8): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178797985 | |||||
| chr1:178797985
|
T | TAAAAA | 6 | a0001c0001t0020g0038a0001c0002t0003g0021a0001c0002t0003g0024others(3): Show | 6 | HG00423.hp1 HG02027.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.214-10044_214-1004 others(9): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178797985 | |||||
| chr1:178797985
|
TA | T | 9 | a0001c0001t0001g0254a0001c0001t0012g0152a0001c0002t0005g0007others(6): Show | 9 | HG00099.hp1 HG01069.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.214-10040delA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178797985 | |||||
| chr1:178798006
|
C | A | 1 | a0001c0001t0006g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.214-10039C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178798006 | ||||||
| chr1:178798291
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.214-9754G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178798291 | ||||||
| chr1:178798303
|
C | T | 1 | a0001c0001t0006g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.214-9742C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178798303 | ||||||
| chr1:178798414
|
C | G | 1 | a0001c0001t0001g0259 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.214-9631C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178798414 | ||||||
| chr1:178798645
|
T | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-9400T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178798645 | ||||||
| chr1:178798646
|
A | T | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-9399A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178798646 | ||||||
| chr1:178798880
|
C | T | 3 | a0001c0001t0010g0068a0001c0001t0010g0069a0001c0001t0010g0070 | 3 | HG02976.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.214-9165C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178798880 | ||||||
| chr1:178798916
|
T | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | NA18954.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.214-9129T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178798916 | ||||||
| chr1:178798975
|
G | C | 51 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(48): Show | 51 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.214-9070G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178798975 | ||||||
| chr1:178799036
|
T | C | 2 | a0001c0001t0021g0075a0001c0001t0021g0076 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.214-9009T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178799036 | ||||||
| chr1:178799063
|
G | A | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.214-8982G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178799063 | ||||||
| chr1:178799127
|
C | A | 2 | a0001c0001t0019g0146a0001c0001t0019g0147 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.214-8918C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178799127 | ||||||
| chr1:178799201
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.214-8844G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178799201 | ||||||
| chr1:178799335
|
A | AACAAGTT others(316): Show |
1 | a0001c0001t0020g0038 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.214-8700_214-8699i others(325): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178799335 | |||||
| chr1:178799335
|
A | AACAAGTT others(317): Show |
1 | a0001c0001t0020g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.214-8700_214-8699i others(326): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178799335 | |||||
| chr1:178799347
|
A | G | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-8698A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178799347 | ||||||
| chr1:178799361
|
G | A | 3 | a0001c0001t0002g0082a0001c0001t0002g0094a0001c0001t0002g0287 | 3 | NA18966.hp1 NA18968.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.214-8684G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178799361 | ||||||
| chr1:178799373
|
A | G | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.214-8672A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178799373 | ||||||
| chr1:178799392
|
G | T | 44 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(41): Show | 44 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.214-8653G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178799392 | ||||||
| chr1:178799422
|
C | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.214-8623C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178799422 | ||||||
| chr1:178799477
|
G | A | 7 | a0001c0001t0006g0045a0001c0001t0008g0112a0001c0001t0008g0113others(4): Show | 7 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.214-8568G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178799477 | ||||||
| chr1:178799676
|
G | T | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01099.hp1 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.214-8369G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178799676 | ||||||
| chr1:178799703
|
C | T | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.214-8342C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178799703 | ||||||
| chr1:178799708
|
G | A | 1 | a0001c0001t0001g0299 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.214-8337G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178799708 | ||||||
| chr1:178800013
|
A | G | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.214-8032A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178800013 | ||||||
| chr1:178800104
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.214-7941C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178800104 | ||||||
| chr1:178800185
|
A | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.214-7860A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178800185 | ||||||
| chr1:178800253
|
A | G | 27 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(24): Show | 27 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.214-7792A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178800253 | ||||||
| chr1:178800448
|
A | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.214-7597A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178800448 | ||||||
| chr1:178800465
|
A | C | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.214-7580A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178800465 | ||||||
| chr1:178800471
|
G | A | 6 | a0001c0001t0002g0090a0001c0001t0002g0091a0001c0001t0002g0104others(3): Show | 6 | NA18946.hp1 NA18993.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.214-7574G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178800471 | ||||||
| chr1:178800503
|
C | T | 1 | a0001c0001t0002g0153 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.214-7542C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178800503 | ||||||
| chr1:178800517
|
TCTTC | T | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-7524_214-7521d others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178800517 | |||||
| chr1:178800588
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.214-7457T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178800588 | ||||||
| chr1:178800694
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0167 | 2 | HG00558.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.214-7351A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178800694 | ||||||
| chr1:178800884
|
C | T | 1 | a0001c0001t0041g0139 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.214-7161C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178800884 | ||||||
| chr1:178800928
|
C | CT | 15 | a0001c0001t0001g0132a0001c0001t0001g0194a0001c0001t0002g0084others(12): Show | 15 | HG01099.hp1 HG01952.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.214-7102dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178800928 | |||||
| chr1:178801089
|
G | A | 1 | a0001c0001t0002g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.214-6956G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178801089 | ||||||
| chr1:178801094
|
T | C | 29 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0154others(26): Show | 29 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.214-6951T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178801094 | ||||||
| chr1:178801338
|
C | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.214-6707C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178801338 | ||||||
| chr1:178801383
|
A | C | 1 | a0001c0001t0006g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.214-6662A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178801383 | ||||||
| chr1:178801474
|
C | T | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.214-6571C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178801474 | ||||||
| chr1:178801490
|
G | A | 51 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(48): Show | 51 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.214-6555G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178801490 | ||||||
| chr1:178801538
|
A | T | 3 | a0001c0001t0002g0095a0001c0002t0023g0005a0001c0002t0023g0006 | 3 | HG02922.hp2 HG03516.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.214-6507A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178801538 | ||||||
| chr1:178801594
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.214-6451G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178801594 | ||||||
| chr1:178801816
|
AAGGG | A | 203 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(200): Show | 203 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.214-6210_214-6207d others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178801816 | |||||
| chr1:178802126
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.214-5919A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178802126 | ||||||
| chr1:178802354
|
A | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.214-5691A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178802354 | ||||||
| chr1:178802443
|
G | C | 2 | a0001c0001t0002g0002a0001c0001t0002g0003 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.214-5602G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178802443 | ||||||
| chr1:178802464
|
A | G | 3 | a0001c0001t0001g0204a0001c0001t0011g0241a0001c0001t0011g0260 | 3 | NA18971.hp2 NA18991.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.214-5581A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178802464 | ||||||
| chr1:178802499
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.214-5546C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178802499 | ||||||
| chr1:178802735
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.214-5310A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178802735 | ||||||
| chr1:178802751
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.214-5294T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178802751 | ||||||
| chr1:178802792
|
CTT | C | 3 | a0001c0001t0006g0048a0001c0001t0006g0049a0001c0001t0006g0050 | 3 | HG02280.hp1 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.214-5248_214-5247d others(4): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178802792 | |||||
| chr1:178802812
|
T | C | 1 | a0001c0002t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.214-5233T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178802812 | ||||||
| chr1:178802821
|
T | G | 2 | a0001c0001t0010g0062a0001c0001t0010g0063 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.214-5224T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178802821 | ||||||
| chr1:178803176
|
G | A | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.214-4869G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178803176 | ||||||
| chr1:178803200
|
A | G | 1 | a0001c0001t0002g0134 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.214-4845A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178803200 | ||||||
| chr1:178803236
|
A | G | 1 | a0001c0001t0001g0175 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.214-4809A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178803236 | ||||||
| chr1:178803309
|
T | C | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.214-4736T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178803309 | ||||||
| chr1:178803456
|
A | ATCCTAAA others(22): Show |
3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.214-4563_214-4562i others(31): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178803456 | |||||
| chr1:178803701
|
ATTTC | A | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.214-4339_214-4336d others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178803701 | |||||
| chr1:178803945
|
A | G | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.214-4100A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178803945 | ||||||
| chr1:178803946
|
T | C | 1 | a0001c0001t0008g0113 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.214-4099T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178803946 | ||||||
| chr1:178803958
|
C | T | 1 | a0001c0002t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.214-4087C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178803958 | ||||||
| chr1:178803974
|
G | A | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-4071G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178803974 | ||||||
| chr1:178804069
|
C | CT | 26 | a0001c0001t0001g0193a0001c0001t0001g0210a0001c0001t0001g0213others(23): Show | 26 | HG00738.hp2 HG01099.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.214-3963dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178804069 | |||||
| chr1:178804069
|
CT | C | 57 | a0001c0001t0001g0238a0001c0001t0002g0002a0001c0001t0002g0003others(54): Show | 57 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.214-3963delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178804069 | |||||
| chr1:178804253
|
C | CT | 13 | a0001c0001t0001g0246a0001c0001t0001g0248a0001c0001t0001g0273others(10): Show | 13 | HG01884.hp2 HG02155.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.214-3776dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178804253 | |||||
| chr1:178804253
|
C | CTT | 52 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(49): Show | 52 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.214-3777_214-3776d others(4): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178804253 | |||||
| chr1:178804253
|
CT | C | 84 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0055others(81): Show | 84 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.214-3776delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178804253 | |||||
| chr1:178804293
|
A | G | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.214-3752A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178804293 | ||||||
| chr1:178804323
|
T | A | 1 | a0001c0001t0001g0197 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.214-3722T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178804323 | ||||||
| chr1:178804370
|
G | A | 1 | a0001c0001t0002g0131 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.214-3675G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178804370 | ||||||
| chr1:178804411
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.214-3634A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178804411 | ||||||
| chr1:178804422
|
C | T | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.214-3623C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178804422 | ||||||
| chr1:178804505
|
C | T | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.214-3540C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178804505 | ||||||
| chr1:178804545
|
G | A | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.214-3500G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178804545 | ||||||
| chr1:178804546
|
C | T | 9 | a0001c0001t0001g0178a0001c0001t0006g0043a0001c0001t0006g0044others(6): Show | 9 | HG01884.hp1 HG02280.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.214-3499C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178804546 | ||||||
| chr1:178804597
|
G | A | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.214-3448G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178804597 | ||||||
| chr1:178804624
|
T | C | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.214-3421T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178804624 | ||||||
| chr1:178804635
|
C | T | 23 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.214-3410C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178804635 | ||||||
| chr1:178804692
|
G | A | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.214-3353G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178804692 | ||||||
| chr1:178804726
|
C | T | 2 | a0001c0002t0005g0036a0001c0002t0005g0037 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.214-3319C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178804726 | ||||||
| chr1:178804727
|
G | A | 3 | a0001c0001t0006g0048a0001c0001t0006g0049a0001c0001t0006g0050 | 3 | HG02280.hp1 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.214-3318G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178804727 | ||||||
| chr1:178804740
|
G | A | 2 | a0001c0001t0002g0002a0001c0001t0002g0003 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.214-3305G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178804740 | ||||||
| chr1:178804875
|
C | T | 1 | a0001c0001t0010g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.214-3170C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178804875 | ||||||
| chr1:178805031
|
G | A | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.214-3014G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178805031 | ||||||
| chr1:178805063
|
G | A | 1 | a0001c0002t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.214-2982G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178805063 | ||||||
| chr1:178805149
|
T | C | 1 | a0001c0001t0009g0141 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.214-2896T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178805149 | ||||||
| chr1:178805222
|
G | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.214-2823G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178805222 | ||||||
| chr1:178805259
|
G | C | 41 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(38): Show | 41 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(38): Show |
intron_variant | MODIFIER | c.214-2786G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178805259 | ||||||
| chr1:178805276
|
A | G | 151 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(148): Show | 151 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.214-2769A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178805276 | ||||||
| chr1:178805306
|
G | T | 9 | a0001c0001t0001g0167a0001c0001t0006g0043a0001c0001t0006g0044others(6): Show | 9 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.214-2739G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178805306 | ||||||
| chr1:178805322
|
C | T | 1 | a0001c0001t0011g0240 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.214-2723C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178805322 | ||||||
| chr1:178805330
|
G | A | 1 | a0001c0001t0009g0142 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.214-2715G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178805330 | ||||||
| chr1:178805381
|
G | A | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.214-2664G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178805381 | ||||||
| chr1:178805471
|
G | A | 37 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(34): Show | 37 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.214-2574G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178805471 | ||||||
| chr1:178805550
|
G | T | 35 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(32): Show | 35 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.214-2495G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178805550 | ||||||
| chr1:178805554
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.214-2491G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178805554 | ||||||
| chr1:178805768
|
A | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.214-2277A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178805768 | ||||||
| chr1:178806090
|
A | T | 2 | a0001c0002t0023g0005a0001c0002t0023g0006 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.214-1955A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178806090 | ||||||
| chr1:178806090
|
AT | A | 15 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(12): Show | 15 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.214-1947delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | 178806090 | |||||
| chr1:178806181
|
A | G | 5 | a0001c0001t0002g0291a0001c0001t0002g0294a0001c0001t0002g0295others(2): Show | 5 | NA18939.hp1 NA18954.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.214-1864A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178806181 | ||||||
| chr1:178806257
|
T | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.214-1788T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178806257 | ||||||
| chr1:178806512
|
C | A | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.214-1533C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178806512 | ||||||
| chr1:178806674
|
G | A | 25 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.214-1371G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178806674 | ||||||
| chr1:178806697
|
T | G | 2 | a0001c0001t0001g0057a0001c0001t0001g0058 | 2 | NA18954.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.214-1348T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178806697 | ||||||
| chr1:178806698
|
G | T | 2 | a0001c0001t0019g0146a0001c0001t0019g0147 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.214-1347G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178806698 | ||||||
| chr1:178806872
|
C | T | 2 | a0001c0002t0005g0036a0001c0002t0005g0037 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.214-1173C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178806872 | ||||||
| chr1:178807039
|
A | G | 2 | a0001c0002t0003g0014a0001c0002t0003g0017 | 2 | NA18952.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.214-1006A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178807039 | ||||||
| chr1:178807227
|
T | C | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.214-818T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178807227 | ||||||
| chr1:178807536
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.214-509T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178807536 | ||||||
| chr1:178807682
|
A | G | 1 | a0001c0001t0002g0289 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.214-363A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178807682 | ||||||
| chr1:178807787
|
T | C | 2 | a0001c0001t0001g0233a0001c0001t0001g0304 | 2 | HG01169.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.214-258T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178807787 | ||||||
| chr1:178807811
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.214-234C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178807811 | ||||||
| chr1:178807836
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.214-209A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178807836 | ||||||
| chr1:178807850
|
G | A | 305 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.214-195G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178807850 | ||||||
| chr1:178808255
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.297+127T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178808255 | ||||||
| chr1:178808495
|
A | C | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.297+367A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178808495 | ||||||
| chr1:178808540
|
T | G | 1 | a0001c0001t0037g0077 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.297+412T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178808540 | ||||||
| chr1:178808559
|
C | G | 5 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.297+431C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178808559 | ||||||
| chr1:178808806
|
A | G | 46 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(43): Show | 46 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.297+678A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178808806 | ||||||
| chr1:178808967
|
C | T | 3 | a0001c0001t0002g0084a0001c0001t0002g0087a0001c0001t0002g0103 | 3 | NA18995.hp1 NA19009.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.297+839C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178808967 | ||||||
| chr1:178809072
|
A | T | 1 | a0001c0001t0001g0196 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.297+944A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178809072 | ||||||
| chr1:178809124
|
G | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.297+996G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178809124 | ||||||
| chr1:178809162
|
T | C | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.297+1034T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178809162 | ||||||
| chr1:178809356
|
A | G | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.297+1228A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178809356 | ||||||
| chr1:178809527
|
A | T | 12 | a0001c0002t0004g0012a0001c0002t0004g0120a0001c0002t0004g0121others(9): Show | 12 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.297+1399A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178809527 | ||||||
| chr1:178809796
|
T | G | 47 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0057others(44): Show | 47 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.298-1519T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178809796 | ||||||
| chr1:178809902
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.298-1413C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178809902 | ||||||
| chr1:178810008
|
C | T | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.298-1307C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178810008 | ||||||
| chr1:178810043
|
T | TG | 17 | a0001c0002t0003g0013a0001c0002t0003g0015a0001c0002t0003g0016others(14): Show | 17 | HG00423.hp1 HG00544.hp1 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.298-1272_298-1271i others(3): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178810043 | ||||||
| chr1:178810199
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.298-1116C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178810199 | ||||||
| chr1:178810452
|
G | A | 37 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(34): Show | 37 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.298-863G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178810452 | ||||||
| chr1:178810530
|
A | AT | 24 | a0001c0001t0001g0201a0001c0001t0001g0269a0001c0001t0006g0043others(21): Show | 24 | HG01884.hp1 HG01978.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.298-769dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr1 | 178810530 | |||||
| chr1:178810530
|
AT | A | 13 | a0001c0001t0001g0298a0001c0001t0002g0295a0001c0001t0007g0064others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.298-769delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | INFO_REALIGN_3_PRIME | chr1 | 178810530 | |||||
| chr1:178810617
|
G | T | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.298-698G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178810617 | ||||||
| chr1:178810672
|
T | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0259 | 2 | HG02293.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.298-643T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178810672 | ||||||
| chr1:178810739
|
C | G | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.298-576C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178810739 | ||||||
| chr1:178810866
|
T | A | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.298-449T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178810866 | ||||||
| chr1:178810884
|
A | G | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.298-431A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178810884 | ||||||
| chr1:178811043
|
T | A | 5 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-272T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178811043 | ||||||
| chr1:178811107
|
A | G | 2 | a0001c0001t0019g0146a0001c0001t0019g0147 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.298-208A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178811107 | ||||||
| chr1:178811114
|
A | C | 13 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.298-201A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178811114 | ||||||
| chr1:178811122
|
C | T | 3 | a0001c0001t0006g0048a0001c0001t0006g0049a0001c0001t0006g0050 | 3 | HG02280.hp1 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.298-193C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 5/19 | chr1 | 178811122 | ||||||
| chr1:178811515
|
A | G | 202 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(199): Show | 202 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.387+111A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178811515 | ||||||
| chr1:178811554
|
C | G | 1 | a0001c0001t0007g0072 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.387+150C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178811554 | ||||||
| chr1:178811558
|
C | A | 1 | a0001c0001t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.387+154C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178811558 | ||||||
| chr1:178811950
|
G | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.387+546G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178811950 | ||||||
| chr1:178811992
|
G | T | 1 | a0001c0001t0006g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.387+588G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178811992 | ||||||
| chr1:178812123
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.387+719T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178812123 | ||||||
| chr1:178812168
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.387+764T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178812168 | ||||||
| chr1:178812364
|
G | A | 27 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(24): Show | 27 | HG01099.hp1 HG01884.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.387+960G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178812364 | ||||||
| chr1:178812466
|
G | C | 1 | a0001c0001t0001g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.387+1062G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178812466 | ||||||
| chr1:178812513
|
T | C | 35 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(32): Show | 35 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.387+1109T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178812513 | ||||||
| chr1:178812558
|
G | A | 1 | a0001c0002t0025g0149 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.387+1154G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178812558 | ||||||
| chr1:178812672
|
G | A | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.387+1268G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178812672 | ||||||
| chr1:178812696
|
A | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.387+1292A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178812696 | ||||||
| chr1:178812740
|
A | T | 1 | a0001c0001t0002g0287 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.387+1336A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178812740 | ||||||
| chr1:178812907
|
T | C | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.387+1503T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178812907 | ||||||
| chr1:178812927
|
A | C | 1 | a0001c0001t0006g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.387+1523A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178812927 | ||||||
| chr1:178812928
|
C | CT | 20 | a0001c0001t0001g0204a0001c0001t0001g0210a0001c0001t0001g0264others(17): Show | 20 | HG00423.hp1 HG01884.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.387+1545dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 178812928 | |||||
| chr1:178812928
|
C | CTT | 7 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(4): Show | 7 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.387+1544_387+1545d others(4): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 178812928 | |||||
| chr1:178812928
|
CT | C | 125 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0155others(122): Show | 125 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.387+1545delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 178812928 | |||||
| chr1:178812995
|
C | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.387+1591C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178812995 | ||||||
| chr1:178813035
|
T | G | 3 | a0001c0001t0002g0082a0001c0001t0002g0094a0001c0001t0002g0287 | 3 | NA18966.hp1 NA18968.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.387+1631T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178813035 | ||||||
| chr1:178813313
|
T | A | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.387+1909T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178813313 | ||||||
| chr1:178813397
|
G | A | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.387+1993G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178813397 | ||||||
| chr1:178813473
|
G | A | 3 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0145 | 3 | HG00558.hp1 HG02040.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.387+2069G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178813473 | ||||||
| chr1:178813477
|
C | T | 2 | a0001c0002t0005g0036a0001c0002t0005g0037 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.387+2073C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178813477 | ||||||
| chr1:178813490
|
A | G | 51 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(48): Show | 51 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.387+2086A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178813490 | ||||||
| chr1:178813699
|
A | G | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.387+2295A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178813699 | ||||||
| chr1:178813856
|
G | A | 1 | a0001c0001t0002g0107 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.387+2452G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178813856 | ||||||
| chr1:178814093
|
A | G | 9 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(6): Show | 9 | HG01069.hp1 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.387+2689A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178814093 | ||||||
| chr1:178814124
|
A | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.387+2720A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178814124 | ||||||
| chr1:178814412
|
G | A | 6 | a0001c0001t0001g0055a0001c0001t0001g0132a0001c0001t0001g0189others(3): Show | 6 | HG00438.hp1 HG01952.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.387+3008G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178814412 | ||||||
| chr1:178814540
|
A | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.387+3136A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178814540 | ||||||
| chr1:178814560
|
C | T | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.387+3156C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178814560 | ||||||
| chr1:178814611
|
T | TTTTTG | 3 | a0001c0001t0019g0146a0001c0001t0019g0147a0001c0001t0036g0137 | 3 | HG02486.hp2 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.387+3224_387+3228d others(7): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 178814611 | |||||
| chr1:178814725
|
C | A | 3 | a0001c0001t0001g0230a0001c0001t0001g0254a0001c0001t0031g0231 | 3 | NA18960.hp1 NA19057.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.387+3321C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178814725 | ||||||
| chr1:178814738
|
C | T | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.387+3334C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178814738 | ||||||
| chr1:178814754
|
G | A | 305 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.387+3350G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178814754 | ||||||
| chr1:178814854
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0191 | 2 | NA18941.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.387+3450C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178814854 | ||||||
| chr1:178815082
|
T | G | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.387+3678T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178815082 | ||||||
| chr1:178815084
|
A | T | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.387+3680A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178815084 | ||||||
| chr1:178815231
|
C | G | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.387+3827C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178815231 | ||||||
| chr1:178815375
|
G | A | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.387+3971G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178815375 | ||||||
| chr1:178815714
|
C | T | 13 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.387+4310C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178815714 | ||||||
| chr1:178815801
|
T | G | 1 | a0001c0001t0011g0257 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.387+4397T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178815801 | ||||||
| chr1:178815850
|
A | G | 1 | a0001c0001t0002g0107 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.387+4446A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178815850 | ||||||
| chr1:178815857
|
A | G | 152 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(149): Show | 152 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.387+4453A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178815857 | ||||||
| chr1:178815933
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.387+4529G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178815933 | ||||||
| chr1:178816077
|
A | G | 1 | a0001c0001t0002g0133 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.387+4673A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178816077 | ||||||
| chr1:178816096
|
T | C | 1 | a0001c0001t0001g0244 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.387+4692T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178816096 | ||||||
| chr1:178816169
|
C | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.387+4765C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178816169 | ||||||
| chr1:178816220
|
T | C | 1 | a0002c0005t0039g0042 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.387+4816T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178816220 | ||||||
| chr1:178816243
|
G | T | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.387+4839G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178816243 | ||||||
| chr1:178816445
|
A | C | 1 | a0001c0001t0001g0161 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.387+5041A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178816445 | ||||||
| chr1:178816511
|
G | T | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.388-5101G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178816511 | ||||||
| chr1:178816645
|
T | C | 152 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(149): Show | 152 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.388-4967T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178816645 | ||||||
| chr1:178816769
|
C | T | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.388-4843C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178816769 | ||||||
| chr1:178816794
|
T | C | 233 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0055others(230): Show | 233 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.388-4818T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178816794 | ||||||
| chr1:178817033
|
G | A | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.388-4579G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178817033 | ||||||
| chr1:178817292
|
C | G | 2 | a0001c0001t0015g0108a0001c0001t0015g0109 | 2 | HG00280.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.388-4320C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178817292 | ||||||
| chr1:178817345
|
TAA | T | 11 | a0001c0001t0001g0243a0001c0001t0001g0264a0001c0001t0001g0277others(8): Show | 11 | HG00642.hp1 HG00738.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.388-4242_388-4241d others(4): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 178817345 | |||||
| chr1:178817345
|
TAAA | T | 269 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(266): Show | 269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.388-4243_388-4241d others(5): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 178817345 | |||||
| chr1:178817345
|
TAAAA | T | 20 | a0001c0001t0001g0210a0001c0001t0002g0078a0001c0001t0006g0048others(17): Show | 20 | HG01256.hp2 HG01346.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.388-4244_388-4241d others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 178817345 | |||||
| chr1:178817345
|
TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0006g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.388-4250_388-4241d others(12): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 178817345 | |||||
| chr1:178817443
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.388-4169G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178817443 | ||||||
| chr1:178817453
|
G | T | 35 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(32): Show | 35 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.388-4159G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178817453 | ||||||
| chr1:178817699
|
T | G | 1 | a0001c0001t0014g0268 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.388-3913T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178817699 | ||||||
| chr1:178817700
|
C | T | 1 | a0001c0002t0023g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.388-3912C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178817700 | ||||||
| chr1:178817736
|
C | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.388-3876C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178817736 | ||||||
| chr1:178817738
|
A | G | 2 | a0001c0002t0023g0005a0001c0002t0023g0006 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.388-3874A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178817738 | ||||||
| chr1:178817873
|
C | A | 1 | a0001c0001t0001g0162 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.388-3739C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178817873 | ||||||
| chr1:178817913
|
G | A | 1 | a0002c0005t0039g0042 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.388-3699G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178817913 | ||||||
| chr1:178818098
|
C | T | 1 | a0001c0002t0025g0149 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.388-3514C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178818098 | ||||||
| chr1:178818228
|
G | C | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.388-3384G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178818228 | ||||||
| chr1:178818346
|
C | G | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.388-3266C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178818346 | ||||||
| chr1:178818512
|
C | T | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.388-3100C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178818512 | ||||||
| chr1:178818556
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0145 | 2 | HG00558.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.388-3056G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178818556 | ||||||
| chr1:178818604
|
A | AGTTCCAT others(7): Show |
21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.388-3006_388-2993d others(16): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 178818604 | |||||
| chr1:178818889
|
T | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.388-2723T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178818889 | ||||||
| chr1:178818990
|
C | CT | 24 | a0001c0001t0001g0216a0001c0001t0001g0251a0001c0001t0001g0264others(21): Show | 24 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.388-2606dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 178818990 | |||||
| chr1:178818990
|
CT | C | 100 | a0001c0001t0001g0194a0001c0001t0001g0263a0001c0001t0002g0002others(97): Show | 100 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.388-2606delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr1 | 178818990 | |||||
| chr1:178819047
|
G | A | 46 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(43): Show | 46 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.388-2565G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819047 | ||||||
| chr1:178819053
|
A | G | 2 | a0001c0002t0023g0005a0001c0002t0023g0006 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.388-2559A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819053 | ||||||
| chr1:178819062
|
C | T | 1 | a0001c0001t0031g0231 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.388-2550C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819062 | ||||||
| chr1:178819145
|
C | T | 2 | a0001c0001t0001g0212a0001c0001t0001g0222 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.388-2467C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819145 | ||||||
| chr1:178819190
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.388-2422G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819190 | ||||||
| chr1:178819208
|
T | G | 151 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(148): Show | 151 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.388-2404T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819208 | ||||||
| chr1:178819240
|
G | C | 1 | a0001c0001t0002g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.388-2372G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819240 | ||||||
| chr1:178819249
|
G | T | 23 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.388-2363G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819249 | ||||||
| chr1:178819257
|
T | C | 1 | a0001c0001t0010g0063 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.388-2355T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819257 | ||||||
| chr1:178819436
|
C | T | 1 | a0001c0001t0001g0191 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.388-2176C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819436 | ||||||
| chr1:178819448
|
G | T | 2 | a0001c0001t0008g0112a0001c0001t0008g0114 | 2 | HG02559.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.388-2164G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819448 | ||||||
| chr1:178819567
|
A | G | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.388-2045A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819567 | ||||||
| chr1:178819568
|
A | G | 2 | a0001c0002t0023g0005a0001c0002t0023g0006 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.388-2044A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819568 | ||||||
| chr1:178819591
|
T | A | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.388-2021T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819591 | ||||||
| chr1:178819625
|
A | C | 2 | a0001c0001t0018g0080a0001c0001t0018g0096 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.388-1987A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819625 | ||||||
| chr1:178819743
|
G | A | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.388-1869G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819743 | ||||||
| chr1:178819778
|
T | G | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.388-1834T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819778 | ||||||
| chr1:178819826
|
G | A | 1 | a0001c0001t0006g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.388-1786G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819826 | ||||||
| chr1:178819932
|
A | G | 1 | a0001c0001t0007g0067 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.388-1680A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178819932 | ||||||
| chr1:178820066
|
A | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.388-1546A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178820066 | ||||||
| chr1:178820264
|
G | A | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.388-1348G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178820264 | ||||||
| chr1:178820636
|
T | C | 33 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(30): Show | 33 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.388-976T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178820636 | ||||||
| chr1:178821419
|
G | C | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.388-193G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178821419 | ||||||
| chr1:178821448
|
T | C | 152 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(149): Show | 152 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.388-164T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178821448 | ||||||
| chr1:178821797
|
T | A | 1 | a0001c0001t0026g0271 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.480+93T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178821797 | ||||||
| chr1:178821972
|
G | A | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.480+268G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178821972 | ||||||
| chr1:178821993
|
A | T | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.480+289A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178821993 | ||||||
| chr1:178822342
|
T | C | 1 | a0001c0001t0012g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.480+638T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178822342 | ||||||
| chr1:178822501
|
C | CTTTT | 31 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(28): Show | 31 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.480+800_480+801ins others(4): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 178822501 | |||||
| chr1:178822623
|
A | G | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.480+919A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178822623 | ||||||
| chr1:178822771
|
A | G | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.480+1067A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178822771 | ||||||
| chr1:178822810
|
T | G | 1 | a0001c0001t0001g0262 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.480+1106T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178822810 | ||||||
| chr1:178822944
|
C | T | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.480+1240C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178822944 | ||||||
| chr1:178822959
|
C | T | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.480+1255C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178822959 | ||||||
| chr1:178823124
|
A | G | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.480+1420A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178823124 | ||||||
| chr1:178823194
|
G | T | 1 | a0001c0001t0026g0271 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.480+1490G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178823194 | ||||||
| chr1:178823420
|
A | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.480+1716A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178823420 | ||||||
| chr1:178823443
|
ATGCTC | A | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.480+1742_480+1746d others(7): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 178823443 | |||||
| chr1:178823578
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.480+1874A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178823578 | ||||||
| chr1:178823589
|
A | G | 3 | a0001c0001t0001g0246a0001c0001t0001g0248a0001c0001t0001g0273 | 3 | HG01884.hp2 HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.480+1885A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178823589 | ||||||
| chr1:178823990
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.480+2286A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178823990 | ||||||
| chr1:178824277
|
A | G | 13 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.480+2573A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178824277 | ||||||
| chr1:178824528
|
G | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.480+2824G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178824528 | ||||||
| chr1:178824584
|
G | A | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.480+2880G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178824584 | ||||||
| chr1:178824635
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.480+2931C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178824635 | ||||||
| chr1:178824669
|
C | T | 2 | a0001c0001t0001g0166a0001c0001t0001g0194 | 2 | HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.480+2965C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178824669 | ||||||
| chr1:178824700
|
T | G | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.480+2996T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178824700 | ||||||
| chr1:178824788
|
G | A | 1 | a0001c0002t0003g0023 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.480+3084G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178824788 | ||||||
| chr1:178824808
|
CAAAAAAA others(3): Show |
C | 46 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(43): Show | 46 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.480+3119_480+3128d others(12): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 178824808 | |||||
| chr1:178824941
|
C | T | 2 | a0001c0001t0018g0080a0001c0001t0018g0096 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.480+3237C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178824941 | ||||||
| chr1:178825026
|
G | A | 1 | a0001c0004t0004g0001 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.480+3322G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178825026 | ||||||
| chr1:178825090
|
A | G | 6 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.480+3386A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178825090 | ||||||
| chr1:178825407
|
A | G | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.480+3703A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178825407 | ||||||
| chr1:178825430
|
G | A | 3 | a0001c0001t0019g0146a0001c0001t0019g0147a0001c0001t0036g0137 | 3 | HG02486.hp2 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.480+3726G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178825430 | ||||||
| chr1:178825447
|
G | A | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.480+3743G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178825447 | ||||||
| chr1:178825473
|
A | G | 7 | a0001c0001t0001g0224a0001c0001t0001g0226a0001c0001t0001g0245others(4): Show | 7 | HG01069.hp1 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.480+3769A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178825473 | ||||||
| chr1:178825840
|
C | T | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.480+4136C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178825840 | ||||||
| chr1:178825841
|
A | T | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.480+4137A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178825841 | ||||||
| chr1:178826107
|
T | C | 1 | a0001c0001t0008g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.480+4403T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178826107 | ||||||
| chr1:178826294
|
A | T | 5 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.480+4590A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178826294 | ||||||
| chr1:178826333
|
A | G | 31 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(28): Show | 31 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.480+4629A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178826333 | ||||||
| chr1:178826377
|
A | G | 1 | a0002c0005t0039g0042 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.480+4673A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178826377 | ||||||
| chr1:178826391
|
C | T | 5 | a0001c0001t0001g0155a0001c0001t0001g0170a0001c0001t0001g0174others(2): Show | 5 | NA18942.hp2 NA18964.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+4687C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178826391 | ||||||
| chr1:178826596
|
T | C | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.480+4892T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178826596 | ||||||
| chr1:178826609
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.480+4905A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178826609 | ||||||
| chr1:178826723
|
A | T | 1 | a0001c0001t0001g0272 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.480+5019A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178826723 | ||||||
| chr1:178826766
|
A | G | 1 | a0001c0001t0002g0100 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.480+5062A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178826766 | ||||||
| chr1:178826821
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.480+5117A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178826821 | ||||||
| chr1:178826874
|
A | C | 2 | a0001c0001t0001g0228a0001c0001t0001g0234 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.480+5170A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178826874 | ||||||
| chr1:178826889
|
C | T | 1 | a0001c0001t0006g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.480+5185C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178826889 | ||||||
| chr1:178827034
|
T | A | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.480+5330T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178827034 | ||||||
| chr1:178827114
|
A | G | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.480+5410A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178827114 | ||||||
| chr1:178827375
|
A | G | 1 | a0001c0001t0001g0282 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.480+5671A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178827375 | ||||||
| chr1:178827380
|
T | C | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.480+5676T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178827380 | ||||||
| chr1:178827387
|
C | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.480+5683C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178827387 | ||||||
| chr1:178827392
|
A | AT | 87 | a0001c0001t0001g0155a0001c0001t0001g0177a0001c0001t0001g0194others(84): Show | 87 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.480+5708dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 178827392 | |||||
| chr1:178827392
|
A | ATT | 19 | a0001c0001t0009g0143a0001c0001t0012g0039a0001c0001t0012g0040others(16): Show | 19 | HG00099.hp1 HG00738.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.480+5707_480+5708d others(4): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 178827392 | |||||
| chr1:178827417
|
C | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.480+5713C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178827417 | ||||||
| chr1:178827434
|
G | A | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.480+5730G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178827434 | ||||||
| chr1:178827454
|
G | A | 13 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.480+5750G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178827454 | ||||||
| chr1:178827480
|
C | T | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.480+5776C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178827480 | ||||||
| chr1:178827495
|
C | T | 9 | a0001c0001t0001g0191a0001c0001t0006g0043a0001c0001t0006g0044others(6): Show | 9 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.480+5791C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178827495 | ||||||
| chr1:178827556
|
G | A | 2 | a0001c0001t0001g0158a0002c0005t0039g0042 | 2 | HG02280.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.480+5852G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178827556 | ||||||
| chr1:178827597
|
A | G | 33 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(30): Show | 33 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.481-5827A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178827597 | ||||||
| chr1:178827691
|
G | A | 1 | a0001c0001t0006g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.481-5733G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178827691 | ||||||
| chr1:178827769
|
T | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.481-5655T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178827769 | ||||||
| chr1:178827808
|
C | T | 3 | a0001c0001t0019g0146a0001c0001t0019g0147a0001c0001t0036g0137 | 3 | HG02486.hp2 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.481-5616C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178827808 | ||||||
| chr1:178828036
|
T | C | 1 | a0001c0001t0032g0180 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.481-5388T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828036 | ||||||
| chr1:178828089
|
A | G | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.481-5335A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828089 | ||||||
| chr1:178828094
|
C | T | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.481-5330C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828094 | ||||||
| chr1:178828196
|
A | T | 4 | a0001c0001t0006g0046a0001c0001t0006g0048a0001c0001t0006g0049others(1): Show | 4 | HG01884.hp1 HG02280.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-5228A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828196 | ||||||
| chr1:178828226
|
G | C | 3 | a0001c0001t0006g0048a0001c0001t0006g0049a0001c0001t0006g0050 | 3 | HG02280.hp1 HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.481-5198G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828226 | ||||||
| chr1:178828257
|
C | T | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.481-5167C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828257 | ||||||
| chr1:178828274
|
T | C | 152 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(149): Show | 152 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.481-5150T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828274 | ||||||
| chr1:178828275
|
G | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.481-5149G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828275 | ||||||
| chr1:178828344
|
C | A | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.481-5080C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828344 | ||||||
| chr1:178828426
|
G | T | 1 | a0001c0001t0002g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.481-4998G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828426 | ||||||
| chr1:178828532
|
G | A | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.481-4892G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828532 | ||||||
| chr1:178828630
|
A | C | 23 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.481-4794A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828630 | ||||||
| chr1:178828643
|
C | T | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.481-4781C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828643 | ||||||
| chr1:178828654
|
C | T | 1 | a0001c0001t0006g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.481-4770C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828654 | ||||||
| chr1:178828669
|
G | A | 1 | a0002c0005t0039g0042 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.481-4755G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828669 | ||||||
| chr1:178828813
|
A | G | 23 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.481-4611A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828813 | ||||||
| chr1:178828828
|
A | G | 43 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(40): Show | 43 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.481-4596A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828828 | ||||||
| chr1:178828828
|
A | T | 1 | a0001c0001t0006g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.481-4596A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828828 | ||||||
| chr1:178828883
|
T | C | 2 | a0001c0002t0005g0036a0001c0002t0005g0037 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.481-4541T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828883 | ||||||
| chr1:178828939
|
A | G | 1 | a0001c0001t0022g0059 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.481-4485A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178828939 | ||||||
| chr1:178829298
|
G | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.481-4126G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178829298 | ||||||
| chr1:178829299
|
G | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.481-4125G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178829299 | ||||||
| chr1:178829393
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.481-4031C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178829393 | ||||||
| chr1:178829450
|
T | C | 16 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0168others(13): Show | 16 | HG00438.hp2 HG00741.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.481-3974T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178829450 | ||||||
| chr1:178829458
|
A | G | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.481-3966A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178829458 | ||||||
| chr1:178829563
|
C | G | 1 | a0001c0002t0005g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.481-3861C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178829563 | ||||||
| chr1:178829641
|
A | G | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.481-3783A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178829641 | ||||||
| chr1:178829679
|
A | G | 1 | a0001c0001t0041g0139 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.481-3745A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178829679 | ||||||
| chr1:178829825
|
A | G | 13 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.481-3599A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178829825 | ||||||
| chr1:178830005
|
A | C | 1 | a0001c0001t0001g0225 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.481-3419A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178830005 | ||||||
| chr1:178830081
|
T | C | 1 | a0001c0002t0005g0008 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.481-3343T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178830081 | ||||||
| chr1:178830305
|
G | C | 33 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(30): Show | 33 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.481-3119G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178830305 | ||||||
| chr1:178830317
|
G | C | 31 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(28): Show | 31 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.481-3107G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178830317 | ||||||
| chr1:178830333
|
G | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.481-3091G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178830333 | ||||||
| chr1:178830536
|
A | G | 3 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0300 | 3 | HG00438.hp1 NA18969.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.481-2888A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178830536 | ||||||
| chr1:178830541
|
G | T | 7 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(4): Show | 7 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.481-2883G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178830541 | ||||||
| chr1:178830739
|
A | G | 1 | a0001c0001t0009g0140 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.481-2685A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178830739 | ||||||
| chr1:178830886
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.481-2538C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178830886 | ||||||
| chr1:178831211
|
G | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.481-2213G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178831211 | ||||||
| chr1:178831346
|
C | T | 194 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(191): Show | 194 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(191): Show |
intron_variant | MODIFIER | c.481-2078C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178831346 | ||||||
| chr1:178831426
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.481-1998G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178831426 | ||||||
| chr1:178831441
|
T | C | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.481-1983T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178831441 | ||||||
| chr1:178831612
|
T | C | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.481-1812T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178831612 | ||||||
| chr1:178831622
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.481-1802G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178831622 | ||||||
| chr1:178831625
|
CCG | C | 20 | a0001c0001t0006g0045a0001c0001t0008g0113a0001c0001t0008g0114others(17): Show | 20 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.481-1797_481-1796d others(4): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr1 | 178831625 | |||||
| chr1:178831626
|
C | T | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.481-1798C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178831626 | ||||||
| chr1:178831626
|
CG | C | 7 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0048others(4): Show | 7 | HG02055.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-1797delG | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178831626 | ||||||
| chr1:178831627
|
G | C | 5 | a0001c0001t0006g0046a0001c0001t0006g0047a0001c0001t0006g0049others(2): Show | 5 | HG01884.hp1 HG02723.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-1797G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178831627 | ||||||
| chr1:178831713
|
T | A | 1 | a0001c0001t0001g0282 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.481-1711T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178831713 | ||||||
| chr1:178831748
|
G | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.481-1676G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178831748 | ||||||
| chr1:178832024
|
G | A | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.481-1400G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178832024 | ||||||
| chr1:178832040
|
G | T | 1 | a0001c0001t0032g0180 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.481-1384G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178832040 | ||||||
| chr1:178832224
|
C | T | 4 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0217others(1): Show | 4 | HG01070.hp1 HG01261.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-1200C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178832224 | ||||||
| chr1:178832247
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.481-1177G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178832247 | ||||||
| chr1:178832278
|
C | T | 2 | a0001c0001t0019g0146a0001c0001t0019g0147 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.481-1146C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178832278 | ||||||
| chr1:178832345
|
C | T | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.481-1079C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178832345 | ||||||
| chr1:178832375
|
C | G | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.481-1049C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178832375 | ||||||
| chr1:178832639
|
T | C | 57 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(54): Show | 57 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.481-785T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178832639 | ||||||
| chr1:178832663
|
G | C | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.481-761G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178832663 | ||||||
| chr1:178832702
|
A | T | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.481-722A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178832702 | ||||||
| chr1:178832703
|
T | A | 4 | a0001c0001t0001g0224a0001c0001t0001g0226a0001c0001t0001g0245others(1): Show | 4 | HG01069.hp1 HG02717.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-721T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178832703 | ||||||
| chr1:178832710
|
G | C | 1 | a0001c0001t0011g0240 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.481-714G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178832710 | ||||||
| chr1:178832778
|
T | G | 9 | a0001c0002t0004g0120a0001c0002t0004g0121a0001c0002t0004g0122others(6): Show | 9 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.481-646T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178832778 | ||||||
| chr1:178832779
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.481-645G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178832779 | ||||||
| chr1:178833112
|
A | T | 3 | a0001c0001t0001g0233a0001c0001t0001g0255a0001c0001t0001g0304 | 3 | HG01123.hp1 HG01169.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.481-312A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178833112 | ||||||
| chr1:178833274
|
G | C | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.481-150G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178833274 | ||||||
| chr1:178833298
|
A | G | 1 | a0001c0001t0001g0183 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.481-126A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178833298 | ||||||
| chr1:178833310
|
G | T | 1 | a0001c0001t0006g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.481-114G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178833310 | ||||||
| chr1:178833589
|
T | C | 1 | a0001c0001t0009g0140 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.607+39T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178833589 | ||||||
| chr1:178833597
|
C | G | 1 | a0001c0001t0001g0200 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.607+47C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178833597 | ||||||
| chr1:178833786
|
G | C | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.607+236G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178833786 | ||||||
| chr1:178833854
|
C | T | 153 | a0001c0001t0001g0132a0001c0001t0001g0177a0001c0001t0002g0002others(150): Show | 153 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.607+304C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178833854 | ||||||
| chr1:178833855
|
G | T | 1 | a0001c0001t0001g0286 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.607+305G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178833855 | ||||||
| chr1:178833985
|
C | G | 53 | a0001c0001t0001g0132a0001c0001t0002g0079a0001c0001t0002g0081others(50): Show | 53 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.607+435C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178833985 | ||||||
| chr1:178834039
|
A | C | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.607+489A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178834039 | ||||||
| chr1:178834232
|
A | C | 23 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.607+682A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178834232 | ||||||
| chr1:178834232
|
A | G | 1 | a0001c0001t0022g0059 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.607+682A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178834232 | ||||||
| chr1:178834359
|
A | G | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.607+809A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178834359 | ||||||
| chr1:178834494
|
A | G | 1 | a0001c0001t0008g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.607+944A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178834494 | ||||||
| chr1:178834688
|
T | C | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.607+1138T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178834688 | ||||||
| chr1:178834836
|
A | G | 152 | a0001c0001t0001g0177a0001c0001t0002g0002a0001c0001t0002g0003others(149): Show | 152 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.607+1286A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178834836 | ||||||
| chr1:178835041
|
G | A | 2 | a0001c0002t0023g0005a0001c0002t0023g0006 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.607+1491G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178835041 | ||||||
| chr1:178835208
|
T | C | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.607+1658T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178835208 | ||||||
| chr1:178835220
|
G | A | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.607+1670G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178835220 | ||||||
| chr1:178835268
|
T | C | 6 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.607+1718T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178835268 | ||||||
| chr1:178835338
|
G | A | 1 | a0002c0005t0039g0042 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.607+1788G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178835338 | ||||||
| chr1:178835392
|
C | CT | 50 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0058others(47): Show | 50 | HG00280.hp2 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.607+1860dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178835392 | |||||
| chr1:178835393
|
T | C | 5 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(2): Show | 5 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.607+1843T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178835393 | ||||||
| chr1:178835424
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+1874G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178835424 | ||||||
| chr1:178835432
|
G | T | 1 | a0001c0001t0006g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.607+1882G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178835432 | ||||||
| chr1:178835478
|
C | T | 11 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(8): Show | 11 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.607+1928C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178835478 | ||||||
| chr1:178835536
|
G | A | 3 | a0001c0001t0001g0195a0001c0001t0001g0220a0001c0001t0001g0227 | 3 | HG01106.hp2 HG01256.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.607+1986G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178835536 | ||||||
| chr1:178835567
|
A | G | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.607+2017A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178835567 | ||||||
| chr1:178836135
|
A | G | 3 | a0001c0001t0002g0089a0001c0001t0002g0100a0001c0001t0002g0136 | 3 | NA18974.hp1 NA19012.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.607+2585A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178836135 | ||||||
| chr1:178836185
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+2635A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178836185 | ||||||
| chr1:178836578
|
T | A | 152 | a0001c0001t0001g0177a0001c0001t0002g0002a0001c0001t0002g0003others(149): Show | 152 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.607+3028T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178836578 | ||||||
| chr1:178836603
|
T | G | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.607+3053T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178836603 | ||||||
| chr1:178836882
|
G | A | 2 | a0001c0001t0019g0146a0001c0001t0019g0147 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.607+3332G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178836882 | ||||||
| chr1:178837102
|
T | C | 2 | a0001c0002t0023g0005a0001c0002t0023g0006 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.607+3552T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178837102 | ||||||
| chr1:178837105
|
A | G | 4 | a0001c0001t0001g0242a0001c0001t0001g0250a0001c0001t0001g0261others(1): Show | 4 | HG00423.hp2 NA18947.hp2 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.607+3555A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178837105 | ||||||
| chr1:178837120
|
T | C | 4 | a0001c0001t0002g0088a0001c0001t0002g0102a0001c0001t0002g0134others(1): Show | 4 | NA18941.hp2 NA18953.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.607+3570T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178837120 | ||||||
| chr1:178837547
|
C | T | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.607+3997C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178837547 | ||||||
| chr1:178837569
|
G | A | 5 | a0001c0001t0006g0046a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.607+4019G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178837569 | ||||||
| chr1:178837603
|
T | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.607+4053T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178837603 | ||||||
| chr1:178837629
|
A | T | 1 | a0001c0001t0002g0107 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.607+4079A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178837629 | ||||||
| chr1:178837709
|
C | CGAGCAT | 300 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(297): Show | 300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.607+4163_607+4164i others(8): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178837709 | |||||
| chr1:178837715
|
G | A | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.607+4165G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178837715 | ||||||
| chr1:178837724
|
C | T | 1 | a0001c0001t0002g0095 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.607+4174C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178837724 | ||||||
| chr1:178837919
|
C | G | 8 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(5): Show | 8 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.607+4369C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178837919 | ||||||
| chr1:178837936
|
A | C | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.607+4386A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178837936 | ||||||
| chr1:178837952
|
G | A | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.607+4402G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178837952 | ||||||
| chr1:178837970
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.607+4420G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178837970 | ||||||
| chr1:178837981
|
A | G | 1 | a0001c0002t0003g0013 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.607+4431A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178837981 | ||||||
| chr1:178838056
|
G | A | 1 | a0001c0002t0003g0025 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.607+4506G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178838056 | ||||||
| chr1:178838057
|
C | T | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.607+4507C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178838057 | ||||||
| chr1:178838176
|
A | G | 33 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(30): Show | 33 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.607+4626A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178838176 | ||||||
| chr1:178838214
|
A | G | 1 | a0001c0002t0005g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.607+4664A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178838214 | ||||||
| chr1:178838307
|
G | A | 13 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.607+4757G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178838307 | ||||||
| chr1:178838319
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.607+4769G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178838319 | ||||||
| chr1:178838414
|
G | C | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+4864G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178838414 | ||||||
| chr1:178838498
|
T | G | 2 | a0001c0001t0001g0217a0001c0001t0028g0187 | 2 | HG02451.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.607+4948T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178838498 | ||||||
| chr1:178838600
|
A | G | 3 | a0001c0001t0014g0267a0001c0001t0014g0268a0001c0001t0014g0275 | 3 | HG00544.hp2 NA18747.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.607+5050A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178838600 | ||||||
| chr1:178838658
|
G | T | 23 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(20): Show | 23 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.607+5108G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178838658 | ||||||
| chr1:178838741
|
G | A | 1 | a0001c0001t0002g0095 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.607+5191G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178838741 | ||||||
| chr1:178838857
|
C | T | 1 | a0001c0001t0001g0225 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.607+5307C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178838857 | ||||||
| chr1:178838951
|
A | G | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.607+5401A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178838951 | ||||||
| chr1:178838967
|
A | AAG | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.607+5418_607+5419d others(4): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178838967 | |||||
| chr1:178839114
|
C | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+5564C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839114 | ||||||
| chr1:178839146
|
C | G | 7 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(4): Show | 7 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.607+5596C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839146 | ||||||
| chr1:178839210
|
C | T | 32 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(29): Show | 32 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.607+5660C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839210 | ||||||
| chr1:178839222
|
A | C | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+5672A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839222 | ||||||
| chr1:178839226
|
T | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+5676T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839226 | ||||||
| chr1:178839270
|
A | G | 153 | a0001c0001t0001g0132a0001c0001t0001g0177a0001c0001t0002g0002others(150): Show | 153 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.607+5720A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839270 | ||||||
| chr1:178839331
|
A | G | 2 | a0001c0001t0001g0242a0001c0001t0001g0269 | 2 | HG00423.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.607+5781A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839331 | ||||||
| chr1:178839353
|
A | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.607+5803A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839353 | ||||||
| chr1:178839467
|
T | G | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+5917T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839467 | ||||||
| chr1:178839491
|
T | C | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+5941T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839491 | ||||||
| chr1:178839494
|
C | A | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+5944C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839494 | ||||||
| chr1:178839499
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+5949G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839499 | ||||||
| chr1:178839514
|
A | G | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+5964A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839514 | ||||||
| chr1:178839536
|
T | C | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+5986T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839536 | ||||||
| chr1:178839545
|
C | A | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+5995C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839545 | ||||||
| chr1:178839546
|
C | T | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+5996C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839546 | ||||||
| chr1:178839547
|
A | G | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+5997A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839547 | ||||||
| chr1:178839556
|
A | T | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+6006A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839556 | ||||||
| chr1:178839566
|
T | A | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+6016T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839566 | ||||||
| chr1:178839571
|
G | A | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+6021G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839571 | ||||||
| chr1:178839579
|
T | C | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+6029T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839579 | ||||||
| chr1:178839580
|
G | A | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+6030G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839580 | ||||||
| chr1:178839582
|
T | G | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+6032T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839582 | ||||||
| chr1:178839587
|
G | T | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+6037G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839587 | ||||||
| chr1:178839600
|
T | G | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+6050T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839600 | ||||||
| chr1:178839605
|
T | C | 55 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(52): Show | 55 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.607+6055T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839605 | ||||||
| chr1:178839608
|
T | C | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+6058T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839608 | ||||||
| chr1:178839609
|
G | T | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+6059G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839609 | ||||||
| chr1:178839624
|
C | G | 55 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(52): Show | 55 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.607+6074C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839624 | ||||||
| chr1:178839625
|
G | T | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+6075G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839625 | ||||||
| chr1:178839664
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+6114A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839664 | ||||||
| chr1:178839707
|
C | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.607+6157C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839707 | ||||||
| chr1:178839835
|
A | T | 3 | a0001c0001t0014g0267a0001c0001t0014g0268a0001c0001t0014g0275 | 3 | HG00544.hp2 NA18747.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.607+6285A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839835 | ||||||
| chr1:178839838
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+6288A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839838 | ||||||
| chr1:178839953
|
A | G | 57 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(54): Show | 57 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.607+6403A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178839953 | ||||||
| chr1:178840027
|
C | T | 2 | a0001c0001t0019g0146a0001c0001t0019g0147 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.607+6477C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178840027 | ||||||
| chr1:178840029
|
T | TA | 6 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.607+6480dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178840029 | |||||
| chr1:178840123
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.607+6573A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178840123 | ||||||
| chr1:178840192
|
A | G | 10 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(7): Show | 10 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.607+6642A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178840192 | ||||||
| chr1:178840218
|
G | T | 1 | a0001c0001t0010g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.607+6668G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178840218 | ||||||
| chr1:178840371
|
G | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.607+6821G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178840371 | ||||||
| chr1:178840446
|
A | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.607+6896A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178840446 | ||||||
| chr1:178840484
|
T | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.607+6934T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178840484 | ||||||
| chr1:178840631
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.607+7081A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178840631 | ||||||
| chr1:178840676
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.607+7126A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178840676 | ||||||
| chr1:178840706
|
A | G | 6 | a0001c0001t0002g0088a0001c0001t0002g0099a0001c0001t0002g0102others(3): Show | 6 | NA18941.hp2 NA18953.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.607+7156A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178840706 | ||||||
| chr1:178840864
|
G | A | 7 | a0001c0001t0001g0193a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01106.hp1 HG01255.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.607+7314G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178840864 | ||||||
| chr1:178840865
|
T | C | 7 | a0001c0001t0001g0193a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01106.hp1 HG01255.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.607+7315T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178840865 | ||||||
| chr1:178840876
|
C | A | 7 | a0001c0001t0001g0193a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01106.hp1 HG01255.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.607+7326C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178840876 | ||||||
| chr1:178840877
|
T | C | 7 | a0001c0001t0001g0193a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01106.hp1 HG01255.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.607+7327T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178840877 | ||||||
| chr1:178840881
|
C | A | 7 | a0001c0001t0001g0193a0001c0001t0001g0209a0001c0001t0001g0210others(4): Show | 7 | HG01106.hp1 HG01255.hp1 HG01952.hp2 others(4): Show |
intron_variant | MODIFIER | c.607+7331C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178840881 | ||||||
| chr1:178840957
|
T | C | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.607+7407T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178840957 | ||||||
| chr1:178841035
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+7485G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178841035 | ||||||
| chr1:178841056
|
A | G | 2 | a0001c0002t0023g0005a0001c0002t0023g0006 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.607+7506A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178841056 | ||||||
| chr1:178841195
|
A | C | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.607+7645A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178841195 | ||||||
| chr1:178841202
|
G | C | 1 | a0001c0002t0023g0005 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.607+7652G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178841202 | ||||||
| chr1:178841234
|
T | G | 6 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.607+7684T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178841234 | ||||||
| chr1:178841322
|
G | C | 1 | a0001c0001t0002g0110 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.607+7772G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178841322 | ||||||
| chr1:178841436
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+7886G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178841436 | ||||||
| chr1:178841600
|
A | G | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.607+8050A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178841600 | ||||||
| chr1:178841660
|
A | G | 2 | a0001c0001t0001g0263a0001c0001t0001g0305 | 2 | NA19062.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.607+8110A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178841660 | ||||||
| chr1:178841687
|
A | G | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.607+8137A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178841687 | ||||||
| chr1:178841756
|
T | C | 97 | a0001c0001t0001g0177a0001c0001t0001g0263a0001c0001t0006g0043others(94): Show | 97 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.607+8206T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178841756 | ||||||
| chr1:178841855
|
C | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.607+8305C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178841855 | ||||||
| chr1:178841891
|
C | T | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.607+8341C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178841891 | ||||||
| chr1:178841912
|
G | A | 5 | a0001c0001t0006g0046a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.607+8362G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178841912 | ||||||
| chr1:178841930
|
A | G | 47 | a0001c0001t0001g0177a0001c0002t0003g0013a0001c0002t0003g0014others(44): Show | 47 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.607+8380A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178841930 | ||||||
| chr1:178841955
|
C | G | 1 | a0001c0001t0001g0167 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.607+8405C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178841955 | ||||||
| chr1:178842000
|
G | C | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.607+8450G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842000 | ||||||
| chr1:178842056
|
C | G | 27 | a0001c0001t0002g0107a0001c0001t0002g0291a0001c0001t0002g0294others(24): Show | 27 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(24): Show |
intron_variant | MODIFIER | c.607+8506C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842056 | ||||||
| chr1:178842123
|
A | C | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.607+8573A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842123 | ||||||
| chr1:178842183
|
C | T | 13 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.607+8633C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842183 | ||||||
| chr1:178842188
|
T | C | 6 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0178others(3): Show | 6 | HG02486.hp2 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.607+8638T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842188 | ||||||
| chr1:178842193
|
A | T | 17 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0168others(14): Show | 17 | HG00438.hp2 HG00741.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.607+8643A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842193 | ||||||
| chr1:178842194
|
G | T | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.607+8644G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842194 | ||||||
| chr1:178842227
|
A | C | 2 | a0001c0001t0026g0271a0001c0001t0036g0137 | 2 | HG02970.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.607+8677A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842227 | ||||||
| chr1:178842233
|
A | G | 1 | a0001c0001t0026g0271 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.607+8683A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842233 | ||||||
| chr1:178842343
|
C | T | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.607+8793C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842343 | ||||||
| chr1:178842358
|
G | A | 3 | a0001c0001t0040g0148a0001c0002t0004g0122a0002c0005t0039g0042 | 3 | HG02280.hp2 HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.607+8808G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842358 | ||||||
| chr1:178842406
|
A | T | 6 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(3): Show | 6 | HG00099.hp1 HG00738.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.607+8856A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842406 | ||||||
| chr1:178842455
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.607+8905G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842455 | ||||||
| chr1:178842558
|
A | C | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.607+9008A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842558 | ||||||
| chr1:178842597
|
G | T | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.607+9047G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842597 | ||||||
| chr1:178842637
|
A | C | 3 | a0001c0001t0037g0077a0001c0002t0005g0036a0001c0002t0005g0037 | 3 | HG01069.hp2 HG01071.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.607+9087A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842637 | ||||||
| chr1:178842644
|
T | A | 1 | a0001c0001t0037g0077 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.607+9094T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842644 | ||||||
| chr1:178842654
|
G | A | 1 | a0001c0001t0002g0107 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.607+9104G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842654 | ||||||
| chr1:178842740
|
T | C | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+9190T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842740 | ||||||
| chr1:178842765
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.607+9215C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842765 | ||||||
| chr1:178842784
|
G | A | 1 | a0001c0001t0016g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.607+9234G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842784 | ||||||
| chr1:178842801
|
T | A | 1 | a0001c0001t0020g0038 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.607+9251T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842801 | ||||||
| chr1:178842830
|
A | C | 1 | a0001c0002t0005g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.607+9280A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842830 | ||||||
| chr1:178842838
|
C | T | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.607+9288C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842838 | ||||||
| chr1:178842947
|
T | A | 1 | a0001c0001t0001g0168 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.607+9397T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842947 | ||||||
| chr1:178842956
|
C | T | 1 | a0001c0001t0022g0059 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.607+9406C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842956 | ||||||
| chr1:178843038
|
G | C | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.607+9488G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178843038 | ||||||
| chr1:178843088
|
A | C | 1 | a0002c0005t0039g0042 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.607+9538A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178843088 | ||||||
| chr1:178843096
|
G | T | 2 | a0001c0001t0002g0107a0001c0002t0025g0149 | 2 | HG03209.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.607+9546G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178843096 | ||||||
| chr1:178843122
|
T | A | 2 | a0001c0001t0029g0156a0001c0002t0025g0149 | 2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.607+9572T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178843122 | ||||||
| chr1:178843166
|
T | G | 23 | a0001c0001t0001g0253a0001c0001t0002g0287a0001c0001t0006g0043others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.607+9616T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178843166 | ||||||
| chr1:178843204
|
G | A | 1 | a0001c0001t0006g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.607+9654G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178843204 | ||||||
| chr1:178843216
|
C | T | 8 | a0001c0001t0001g0212a0001c0001t0001g0222a0001c0001t0012g0039others(5): Show | 8 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.607+9666C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178843216 | ||||||
| chr1:178843482
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.607+9932A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178843482 | ||||||
| chr1:178843501
|
G | T | 7 | a0001c0001t0002g0085a0001c0001t0012g0039a0001c0001t0012g0040others(4): Show | 7 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.607+9951G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178843501 | ||||||
| chr1:178843511
|
G | A | 9 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(6): Show | 9 | HG01069.hp1 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.607+9961G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178843511 | ||||||
| chr1:178843529
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+9979G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178843529 | ||||||
| chr1:178843576
|
T | C | 153 | a0001c0001t0001g0132a0001c0001t0001g0177a0001c0001t0002g0002others(150): Show | 153 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.607+10026T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178843576 | ||||||
| chr1:178843625
|
T | C | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.607+10075T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178843625 | ||||||
| chr1:178843638
|
A | G | 204 | a0001c0001t0001g0056a0001c0001t0001g0132a0001c0001t0001g0155others(201): Show | 204 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(201): Show |
intron_variant | MODIFIER | c.607+10088A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178843638 | ||||||
| chr1:178843654
|
T | TA | 14 | a0001c0001t0001g0217a0001c0001t0007g0064a0001c0001t0007g0065others(11): Show | 14 | HG02257.hp1 HG02451.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.607+10117dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178843654 | |||||
| chr1:178843686
|
A | G | 1 | a0001c0001t0020g0004 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.607+10136A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178843686 | ||||||
| chr1:178843871
|
T | A | 5 | a0001c0001t0001g0056a0001c0001t0001g0252a0001c0001t0001g0256others(2): Show | 5 | HG00438.hp2 HG00741.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.607+10321T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178843871 | ||||||
| chr1:178844237
|
C | A | 151 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(148): Show | 151 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.607+10687C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178844237 | ||||||
| chr1:178844396
|
G | A | 82 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(79): Show | 82 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.607+10846G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178844396 | ||||||
| chr1:178844527
|
T | G | 1 | a0001c0001t0001g0165 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.607+10977T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178844527 | ||||||
| chr1:178844798
|
T | C | 1 | a0001c0002t0003g0032 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.607+11248T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178844798 | ||||||
| chr1:178844815
|
A | G | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.607+11265A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178844815 | ||||||
| chr1:178844818
|
C | A | 2 | a0001c0001t0019g0146a0001c0001t0019g0147 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.607+11268C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178844818 | ||||||
| chr1:178844917
|
T | C | 29 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(26): Show | 29 | HG00738.hp2 HG01884.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.607+11367T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178844917 | ||||||
| chr1:178845101
|
C | CA | 28 | a0001c0001t0001g0056a0001c0001t0001g0179a0001c0001t0001g0186others(25): Show | 28 | HG00438.hp2 HG00642.hp2 HG01346.hp2 others(25): Show |
intron_variant | MODIFIER | c.607+11567dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178845101 | |||||
| chr1:178845164
|
G | A | 33 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(30): Show | 33 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.607+11614G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178845164 | ||||||
| chr1:178845282
|
G | A | 151 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(148): Show | 151 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.607+11732G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178845282 | ||||||
| chr1:178845367
|
G | T | 1 | a0001c0002t0005g0009 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.607+11817G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178845367 | ||||||
| chr1:178845441
|
A | G | 2 | a0001c0002t0023g0005a0001c0002t0023g0006 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.607+11891A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178845441 | ||||||
| chr1:178845562
|
A | G | 37 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(34): Show | 37 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.607+12012A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178845562 | ||||||
| chr1:178845581
|
C | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.607+12031C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178845581 | ||||||
| chr1:178845806
|
T | C | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.607+12256T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178845806 | ||||||
| chr1:178846013
|
A | G | 149 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(146): Show | 149 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.607+12463A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178846013 | ||||||
| chr1:178846037
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+12487G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178846037 | ||||||
| chr1:178846323
|
A | G | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.607+12773A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178846323 | ||||||
| chr1:178846904
|
T | C | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.607+13354T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178846904 | ||||||
| chr1:178846978
|
T | G | 33 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(30): Show | 33 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.607+13428T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178846978 | ||||||
| chr1:178847203
|
T | C | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.607+13653T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178847203 | ||||||
| chr1:178847213
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.607+13663A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178847213 | ||||||
| chr1:178847371
|
G | A | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.607+13821G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178847371 | ||||||
| chr1:178847416
|
A | G | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.607+13866A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178847416 | ||||||
| chr1:178847593
|
G | A | 1 | a0001c0001t0001g0266 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.607+14043G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178847593 | ||||||
| chr1:178847772
|
T | C | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+14222T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178847772 | ||||||
| chr1:178847801
|
G | A | 3 | a0001c0001t0001g0213a0001c0001t0001g0214a0001c0001t0001g0284 | 3 | NA18747.hp2 NA19067.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.607+14251G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178847801 | ||||||
| chr1:178847846
|
G | T | 1 | a0001c0001t0035g0093 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.607+14296G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178847846 | ||||||
| chr1:178847867
|
T | C | 1 | a0001c0002t0004g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.607+14317T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178847867 | ||||||
| chr1:178848114
|
A | T | 1 | a0001c0001t0001g0188 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.607+14564A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178848114 | ||||||
| chr1:178848267
|
T | C | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.607+14717T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178848267 | ||||||
| chr1:178848279
|
C | T | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.607+14729C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178848279 | ||||||
| chr1:178848282
|
G | T | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.607+14732G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178848282 | ||||||
| chr1:178848303
|
C | T | 3 | a0001c0002t0003g0020a0001c0002t0003g0022a0001c0002t0003g0031 | 3 | NA18942.hp1 NA18994.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.607+14753C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178848303 | ||||||
| chr1:178848311
|
A | T | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.607+14761A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178848311 | ||||||
| chr1:178848344
|
T | C | 2 | a0001c0001t0001g0212a0001c0001t0001g0222 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.607+14794T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178848344 | ||||||
| chr1:178848373
|
T | C | 1 | a0001c0001t0006g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.607+14823T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178848373 | ||||||
| chr1:178848438
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+14888G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178848438 | ||||||
| chr1:178848555
|
G | T | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.607+15005G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178848555 | ||||||
| chr1:178848588
|
T | G | 33 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(30): Show | 33 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.607+15038T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178848588 | ||||||
| chr1:178848746
|
C | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+15196C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178848746 | ||||||
| chr1:178848857
|
T | C | 83 | a0001c0001t0001g0177a0001c0001t0006g0043a0001c0001t0006g0044others(80): Show | 83 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.607+15307T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178848857 | ||||||
| chr1:178848917
|
A | G | 47 | a0001c0001t0001g0177a0001c0002t0003g0013a0001c0002t0003g0014others(44): Show | 47 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.607+15367A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178848917 | ||||||
| chr1:178849113
|
A | T | 2 | a0001c0001t0002g0078a0001c0001t0037g0077 | 2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.607+15563A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178849113 | ||||||
| chr1:178849274
|
G | A | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.607+15724G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178849274 | ||||||
| chr1:178849342
|
A | G | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.607+15792A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178849342 | ||||||
| chr1:178849420
|
GGTTGTAT | G | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.607+15875_607+1588 others(11): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178849420 | |||||
| chr1:178849517
|
A | G | 5 | a0001c0002t0003g0014a0001c0002t0003g0017a0001c0002t0003g0020others(2): Show | 5 | NA18942.hp1 NA18952.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.607+15967A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178849517 | ||||||
| chr1:178849619
|
C | CA | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.607+16070dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178849619 | |||||
| chr1:178849639
|
G | C | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.607+16089G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178849639 | ||||||
| chr1:178849929
|
T | A | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.607+16379T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178849929 | ||||||
| chr1:178850111
|
C | G | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.607+16561C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178850111 | ||||||
| chr1:178850219
|
T | C | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.607+16669T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178850219 | ||||||
| chr1:178850238
|
A | G | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG01070.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.607+16688A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178850238 | ||||||
| chr1:178850282
|
T | G | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.607+16732T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178850282 | ||||||
| chr1:178850320
|
A | T | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.607+16770A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178850320 | ||||||
| chr1:178850418
|
A | G | 47 | a0001c0001t0001g0177a0001c0002t0003g0013a0001c0002t0003g0014others(44): Show | 47 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.607+16868A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178850418 | ||||||
| chr1:178850453
|
T | G | 1 | a0001c0001t0001g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.607+16903T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178850453 | ||||||
| chr1:178850505
|
G | GT | 18 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(15): Show | 18 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.607+16964dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178850505 | |||||
| chr1:178850509
|
T | C | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.607+16959T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178850509 | ||||||
| chr1:178850706
|
T | C | 2 | a0001c0002t0005g0036a0001c0002t0005g0037 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.607+17156T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178850706 | ||||||
| chr1:178850801
|
A | C | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.607+17251A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178850801 | ||||||
| chr1:178850903
|
CATA | C | 10 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(7): Show | 10 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.607+17356_607+1735 others(7): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178850903 | |||||
| chr1:178851018
|
A | T | 1 | a0001c0001t0022g0059 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.607+17468A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178851018 | ||||||
| chr1:178851024
|
C | A | 201 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(198): Show | 201 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.607+17474C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178851024 | ||||||
| chr1:178851123
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.607+17573C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178851123 | ||||||
| chr1:178851192
|
G | A | 29 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0154others(26): Show | 29 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.607+17642G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178851192 | ||||||
| chr1:178851336
|
A | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.607+17786A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178851336 | ||||||
| chr1:178851391
|
T | C | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.607+17841T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178851391 | ||||||
| chr1:178851510
|
C | CT | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.607+17967dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178851510 | |||||
| chr1:178851548
|
TA | T | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.607+18003delA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178851548 | |||||
| chr1:178851661
|
C | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+18111C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178851661 | ||||||
| chr1:178851679
|
T | C | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.607+18129T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178851679 | ||||||
| chr1:178851703
|
T | C | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.607+18153T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178851703 | ||||||
| chr1:178851795
|
A | G | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.607+18245A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178851795 | ||||||
| chr1:178851853
|
A | C | 6 | a0001c0001t0001g0055a0001c0001t0001g0132a0001c0001t0001g0189others(3): Show | 6 | HG00438.hp1 HG01952.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.607+18303A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178851853 | ||||||
| chr1:178852185
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.607+18635G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178852185 | ||||||
| chr1:178852291
|
T | C | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.607+18741T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178852291 | ||||||
| chr1:178852468
|
T | C | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.607+18918T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178852468 | ||||||
| chr1:178852705
|
G | A | 9 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(6): Show | 9 | HG01069.hp1 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.607+19155G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178852705 | ||||||
| chr1:178853033
|
C | G | 2 | a0001c0001t0006g0043a0001c0001t0006g0044 | 2 | HG02886.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.607+19483C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178853033 | ||||||
| chr1:178853230
|
T | C | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.607+19680T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178853230 | ||||||
| chr1:178853251
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.607+19701A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178853251 | ||||||
| chr1:178853264
|
G | C | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.607+19714G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178853264 | ||||||
| chr1:178853352
|
G | C | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.607+19802G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178853352 | ||||||
| chr1:178853448
|
AT | A | 3 | a0001c0001t0002g0078a0001c0001t0037g0077a0001c0003t0017g0150 | 3 | HG01243.hp1 HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.607+19905delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178853448 | |||||
| chr1:178853748
|
T | C | 1 | a0001c0001t0002g0082 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.607+20198T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178853748 | ||||||
| chr1:178853906
|
T | C | 1 | a0001c0001t0015g0109 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.607+20356T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178853906 | ||||||
| chr1:178854018
|
A | G | 1 | a0001c0002t0004g0124 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.607+20468A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178854018 | ||||||
| chr1:178854101
|
A | G | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.607+20551A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178854101 | ||||||
| chr1:178854411
|
T | C | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.607+20861T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178854411 | ||||||
| chr1:178854428
|
C | G | 2 | a0001c0001t0002g0099a0001c0001t0002g0135 | 2 | NA18985.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.607+20878C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178854428 | ||||||
| chr1:178854503
|
A | G | 2 | a0001c0001t0019g0146a0001c0001t0019g0147 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.607+20953A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178854503 | ||||||
| chr1:178854844
|
A | G | 5 | a0001c0001t0006g0046a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.607+21294A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178854844 | ||||||
| chr1:178854988
|
T | G | 1 | a0001c0001t0001g0283 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.607+21438T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178854988 | ||||||
| chr1:178855075
|
C | T | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.607+21525C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178855075 | ||||||
| chr1:178855281
|
C | G | 50 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(47): Show | 50 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.607+21731C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178855281 | ||||||
| chr1:178855296
|
CT | C | 65 | a0001c0001t0002g0083a0001c0001t0002g0131a0001c0001t0007g0064others(62): Show | 65 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.607+21763delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178855296 | |||||
| chr1:178855296
|
CTT | C | 23 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.607+21762_607+2176 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178855296 | |||||
| chr1:178855574
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.608-21924G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178855574 | ||||||
| chr1:178855608
|
C | A | 1 | a0001c0001t0035g0093 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.608-21890C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178855608 | ||||||
| chr1:178855620
|
T | C | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.608-21878T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178855620 | ||||||
| chr1:178855635
|
T | G | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.608-21863T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178855635 | ||||||
| chr1:178855699
|
A | G | 2 | a0001c0002t0023g0005a0001c0002t0023g0006 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.608-21799A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178855699 | ||||||
| chr1:178855890
|
G | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.608-21608G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178855890 | ||||||
| chr1:178855909
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.608-21589T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178855909 | ||||||
| chr1:178856190
|
CAG | C | 27 | a0001c0001t0001g0161a0001c0001t0001g0166a0001c0001t0001g0193others(24): Show | 27 | HG00544.hp1 HG00558.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.608-21296_608-2129 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856190 | |||||
| chr1:178856190
|
CAGAG | C | 17 | a0001c0001t0001g0167a0001c0002t0003g0013a0001c0002t0003g0014others(14): Show | 17 | HG00423.hp1 HG00642.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.608-21298_608-2129 others(8): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856190 | |||||
| chr1:178856190
|
CAGAGAGA others(1): Show |
C | 3 | a0001c0002t0004g0122a0001c0002t0004g0124a0001c0002t0004g0125 | 3 | HG01192.hp1 HG02615.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.608-21302_608-2129 others(12): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856190 | |||||
| chr1:178856194
|
G | GATATATA others(5): Show |
1 | a0001c0004t0004g0001 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.608-21303_608-2130 others(16): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856194 | |||||
| chr1:178856194
|
G | GATATATA others(9): Show |
1 | a0001c0001t0012g0041 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.608-21303_608-2130 others(20): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856194 | |||||
| chr1:178856194
|
G | GATATATA others(15): Show |
1 | a0001c0001t0012g0039 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.608-21303_608-2130 others(26): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856194 | |||||
| chr1:178856194
|
G | GATATATA others(17): Show |
1 | a0001c0001t0012g0040 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.608-21303_608-2130 others(28): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856194 | |||||
| chr1:178856194
|
GAGAGAGA others(3): Show |
G | 5 | a0001c0002t0004g0120a0001c0002t0004g0121a0001c0002t0004g0127others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.608-21302_608-2129 others(14): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856194 | |||||
| chr1:178856194
|
GAGAGAGA others(21): Show |
G | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.608-21302_608-2127 others(32): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856194 | |||||
| chr1:178856196
|
G | GATATATA others(17): Show |
1 | a0001c0002t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.608-21301_608-2130 others(28): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856196 | |||||
| chr1:178856196
|
G | T | 7 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(4): Show | 7 | HG00738.hp2 HG02698.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.608-21302G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856196 | ||||||
| chr1:178856198
|
G | GAT | 3 | a0001c0001t0009g0138a0001c0001t0009g0142a0001c0001t0009g0143 | 3 | HG02258.hp2 HG02965.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.608-21299_608-2129 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856198 | |||||
| chr1:178856198
|
G | GATATATA others(13): Show |
1 | a0001c0001t0006g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.608-21299_608-2129 others(24): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856198 | |||||
| chr1:178856198
|
G | GATATATA others(15): Show |
1 | a0001c0001t0006g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.608-21299_608-2129 others(26): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856198 | |||||
| chr1:178856198
|
G | T | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG02109.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.608-21300G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856198 | ||||||
| chr1:178856198
|
GAGAGATA others(11): Show |
G | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.608-21298_608-2128 others(22): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856198 | |||||
| chr1:178856200
|
G | T | 22 | a0001c0001t0006g0046a0001c0001t0006g0047a0001c0001t0008g0112others(19): Show | 22 | HG00738.hp2 HG01884.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.608-21298G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856200 | ||||||
| chr1:178856202
|
G | GAGAGATA others(9): Show |
2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.608-21295_608-2129 others(20): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856202
|
G | GAGAGATA others(11): Show |
1 | a0001c0002t0005g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.608-21295_608-2129 others(22): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856202
|
G | GAGAGATA others(23): Show |
2 | a0001c0001t0021g0075a0001c0001t0021g0076 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.608-21295_608-2129 others(34): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856202
|
G | GAGAGATA others(25): Show |
1 | a0001c0002t0025g0149 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.608-21295_608-2129 others(36): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856202
|
G | GAGATATA others(7): Show |
1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.608-21295_608-2129 others(18): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856202
|
G | GAGATATA others(11): Show |
1 | a0001c0001t0006g0050 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.608-21295_608-2129 others(22): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856202
|
G | GAGATATA others(15): Show |
1 | a0001c0001t0006g0049 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.608-21295_608-2129 others(26): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856202
|
G | GAGATATA others(17): Show |
1 | a0001c0001t0009g0144 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.608-21295_608-2129 others(28): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856202
|
G | GAGATATA others(19): Show |
1 | a0001c0001t0006g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.608-21295_608-2129 others(30): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856202
|
G | GAT | 11 | a0001c0001t0001g0051a0001c0001t0001g0193a0001c0001t0001g0209others(8): Show | 11 | HG01070.hp1 HG01106.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.608-21265_608-2126 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856202
|
G | GATAT | 4 | a0001c0001t0001g0054a0001c0001t0001g0212a0001c0001t0001g0222others(1): Show | 4 | HG02970.hp2 NA18906.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.608-21267_608-2126 others(8): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856202
|
G | GATATAT | 3 | a0001c0001t0001g0299a0001c0001t0013g0221a0001c0001t0022g0059 | 3 | HG01358.hp1 HG01978.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.608-21269_608-2126 others(10): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856202
|
G | GATATATA others(5): Show |
1 | a0001c0001t0008g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.608-21275_608-2126 others(16): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856202
|
G | GATATATA others(7): Show |
2 | a0001c0001t0008g0114a0001c0001t0008g0119 | 2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.608-21277_608-2126 others(18): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856202
|
G | GATATATA others(9): Show |
1 | a0001c0001t0008g0118 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.608-21279_608-2126 others(20): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856202
|
G | GATATATA others(13): Show |
2 | a0001c0001t0008g0112a0001c0001t0008g0113 | 2 | HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.608-21283_608-2126 others(24): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856202
|
G | T | 27 | a0001c0001t0001g0161a0001c0001t0001g0215a0001c0001t0001g0285others(24): Show | 27 | HG00558.hp2 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.608-21296G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856202 | ||||||
| chr1:178856202
|
GAT | G | 79 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0055others(76): Show | 79 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.608-21265_608-2126 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856202
|
GATAT | G | 36 | a0001c0001t0001g0056a0001c0001t0001g0158a0001c0001t0001g0160others(33): Show | 36 | HG00438.hp2 HG00597.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.608-21267_608-2126 others(8): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856202
|
GATATATA others(3): Show |
G | 7 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(4): Show | 7 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.608-21273_608-2126 others(14): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856202 | |||||
| chr1:178856204
|
T | G | 4 | a0001c0001t0001g0219a0001c0001t0001g0263a0001c0001t0001g0276others(1): Show | 4 | HG03492.hp1 NA18978.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.608-21294T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856204 | ||||||
| chr1:178856206
|
T | G | 10 | a0001c0001t0001g0055a0001c0001t0001g0060a0001c0001t0001g0145others(7): Show | 10 | HG00438.hp1 HG00558.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.608-21292T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856206 | ||||||
| chr1:178856212
|
T | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.608-21286T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856212 | ||||||
| chr1:178856214
|
T | G | 9 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0002t0005g0007others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.608-21284T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856214 | ||||||
| chr1:178856216
|
T | G | 7 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(4): Show | 7 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.608-21282T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856216 | ||||||
| chr1:178856220
|
T | G | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.608-21278T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856220 | ||||||
| chr1:178856232
|
T | C | 2 | a0001c0001t0021g0075a0001c0001t0021g0076 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.608-21266T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856232 | ||||||
| chr1:178856234
|
T | C | 2 | a0001c0001t0021g0075a0001c0001t0021g0076 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.608-21264T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856234 | ||||||
| chr1:178856234
|
T | TATATATA others(15): Show |
2 | a0001c0002t0023g0005a0001c0002t0023g0006 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.608-21264_608-2126 others(26): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856234 | ||||||
| chr1:178856234
|
T | TATATATA others(19): Show |
1 | a0001c0001t0012g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.608-21264_608-2126 others(30): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856234 | ||||||
| chr1:178856249
|
T | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.608-21249T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856249 | ||||||
| chr1:178856252
|
T | C | 1 | a0001c0001t0002g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.608-21246T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856252 | ||||||
| chr1:178856394
|
A | AT | 24 | a0001c0001t0001g0060a0001c0001t0001g0145a0001c0001t0001g0193others(21): Show | 24 | HG00558.hp1 HG00733.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.608-21072dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
A | ATT | 6 | a0001c0001t0001g0057a0001c0001t0001g0222a0001c0001t0001g0242others(3): Show | 6 | HG00423.hp2 HG01106.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.608-21073_608-2107 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
A | ATTT | 10 | a0001c0001t0001g0058a0001c0001t0001g0212a0001c0001t0001g0228others(7): Show | 10 | HG02622.hp1 HG02895.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.608-21074_608-2107 others(7): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
A | ATTTT | 8 | a0001c0001t0001g0264a0001c0001t0001g0277a0001c0002t0004g0124others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.608-21075_608-2107 others(8): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
A | ATTTTTTT others(1): Show |
6 | a0001c0001t0002g0134a0001c0002t0005g0008a0001c0002t0005g0009others(3): Show | 6 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.608-21079_608-2107 others(12): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
A | ATTTTTTT others(2): Show |
24 | a0001c0001t0002g0081a0001c0001t0002g0084a0001c0001t0002g0085others(21): Show | 24 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.608-21080_608-2107 others(13): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
A | ATTTTTTT others(3): Show |
15 | a0001c0001t0002g0086a0001c0001t0002g0088a0001c0001t0002g0090others(12): Show | 15 | HG00741.hp2 HG01361.hp2 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.608-21081_608-2107 others(14): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
A | ATTTTTTT others(4): Show |
13 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0083others(10): Show | 13 | HG01074.hp1 HG01099.hp2 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.608-21082_608-2107 others(15): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
A | ATTTTTTT others(5): Show |
3 | a0001c0001t0007g0064a0001c0001t0019g0146a0001c0002t0004g0012 | 3 | HG02109.hp1 HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.608-21083_608-2107 others(16): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
A | ATTTTTTT others(6): Show |
5 | a0001c0001t0007g0065a0001c0001t0007g0066a0001c0001t0019g0147others(2): Show | 5 | HG01074.hp2 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.608-21084_608-2107 others(17): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
A | ATTTTTTT others(7): Show |
2 | a0001c0001t0002g0078a0001c0002t0004g0129 | 2 | HG02818.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.608-21085_608-2107 others(18): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0012g0041 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.608-21086_608-2107 others(19): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
A | ATTTTTTT others(9): Show |
2 | a0001c0001t0002g0289a0001c0001t0010g0074 | 2 | HG00639.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.608-21087_608-2107 others(20): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
A | ATTTTTTT others(10): Show |
3 | a0001c0001t0002g0079a0001c0001t0010g0068a0001c0004t0004g0001 | 3 | HG02083.hp1 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.608-21088_608-2107 others(21): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
A | ATTTTTTT others(12): Show |
1 | a0001c0002t0025g0149 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.608-21090_608-2107 others(23): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
A | ATTTTTTT others(13): Show |
2 | a0001c0001t0010g0062a0001c0001t0010g0069 | 2 | HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.608-21091_608-2107 others(24): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
A | ATTTTTTT others(14): Show |
1 | a0001c0001t0007g0067 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.608-21092_608-2107 others(25): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
A | ATTTTTTT others(15): Show |
2 | a0001c0001t0007g0071a0001c0001t0010g0070 | 2 | HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.608-21093_608-2107 others(26): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
AT | A | 39 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0160others(36): Show | 39 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.608-21072delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
ATTT | A | 9 | a0001c0001t0001g0177a0001c0001t0006g0044a0001c0001t0006g0045others(6): Show | 9 | HG01884.hp1 HG02109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.608-21074_608-2107 others(7): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
ATTTTT | A | 9 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0119others(6): Show | 9 | HG02055.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.608-21076_608-2107 others(9): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
ATTTTTT | A | 24 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0142others(21): Show | 24 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.608-21077_608-2107 others(10): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856394
|
ATTTTTTT others(3): Show |
A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.608-21081_608-2107 others(14): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856394 | |||||
| chr1:178856420
|
T | TTTTTTTT others(5): Show |
1 | a0001c0002t0005g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.608-21072_608-2107 others(16): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856420 | |||||
| chr1:178856425
|
T | TTTTTTTT others(5): Show |
4 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0098others(1): Show | 4 | NA18959.hp2 NA18983.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.608-21072_608-2107 others(16): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856425 | |||||
| chr1:178856425
|
T | TTTTTTTT others(9): Show |
1 | a0001c0001t0002g0287 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.608-21072_608-2107 others(20): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856425 | |||||
| chr1:178856425
|
T | TTTTTTTT others(11): Show |
1 | a0001c0001t0002g0094 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.608-21072_608-2107 others(22): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856425 | |||||
| chr1:178856425
|
T | TTTTTTTT others(15): Show |
1 | a0001c0001t0002g0082 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.608-21072_608-2107 others(26): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178856425 | |||||
| chr1:178856479
|
A | G | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.608-21019A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856479 | ||||||
| chr1:178856491
|
G | A | 1 | a0001c0001t0001g0215 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.608-21007G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856491 | ||||||
| chr1:178856740
|
G | C | 1 | a0001c0002t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.608-20758G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856740 | ||||||
| chr1:178856761
|
T | C | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.608-20737T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856761 | ||||||
| chr1:178856794
|
G | T | 2 | a0001c0001t0001g0256a0001c0001t0001g0301 | 2 | HG01257.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.608-20704G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856794 | ||||||
| chr1:178856991
|
T | A | 7 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(4): Show | 7 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.608-20507T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178856991 | ||||||
| chr1:178857046
|
T | C | 5 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.608-20452T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178857046 | ||||||
| chr1:178857124
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.608-20374G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178857124 | ||||||
| chr1:178857147
|
A | G | 151 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(148): Show | 151 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.608-20351A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178857147 | ||||||
| chr1:178857719
|
C | G | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.608-19779C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178857719 | ||||||
| chr1:178857927
|
A | G | 202 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(199): Show | 202 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.608-19571A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178857927 | ||||||
| chr1:178857932
|
G | T | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | NA18959.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.608-19566G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178857932 | ||||||
| chr1:178857954
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.608-19544T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178857954 | ||||||
| chr1:178857959
|
T | G | 1 | a0001c0001t0001g0229 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.608-19539T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178857959 | ||||||
| chr1:178858028
|
T | C | 57 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(54): Show | 57 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.608-19470T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178858028 | ||||||
| chr1:178858073
|
G | A | 1 | a0002c0005t0039g0042 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.608-19425G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178858073 | ||||||
| chr1:178858088
|
T | C | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.608-19410T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178858088 | ||||||
| chr1:178858159
|
T | C | 1 | a0001c0001t0006g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.608-19339T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178858159 | ||||||
| chr1:178858273
|
T | G | 1 | a0001c0001t0028g0187 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.608-19225T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178858273 | ||||||
| chr1:178858577
|
T | A | 1 | a0001c0001t0001g0154 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.608-18921T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178858577 | ||||||
| chr1:178858729
|
G | A | 151 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(148): Show | 151 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.608-18769G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178858729 | ||||||
| chr1:178858766
|
T | C | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.608-18732T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178858766 | ||||||
| chr1:178858824
|
C | T | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.608-18674C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178858824 | ||||||
| chr1:178858894
|
C | A | 3 | a0001c0001t0002g0084a0001c0001t0002g0087a0001c0001t0002g0103 | 3 | NA18995.hp1 NA19009.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.608-18604C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178858894 | ||||||
| chr1:178858952
|
A | C | 1 | a0001c0001t0033g0202 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.608-18546A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178858952 | ||||||
| chr1:178859141
|
C | CTTTTT | 152 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(149): Show | 152 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.608-18353_608-1835 others(9): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178859141 | |||||
| chr1:178859195
|
C | T | 1 | a0001c0001t0019g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.608-18303C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178859195 | ||||||
| chr1:178859296
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.608-18202G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178859296 | ||||||
| chr1:178859401
|
C | CT | 77 | a0001c0001t0001g0132a0001c0001t0001g0163a0001c0001t0001g0164others(74): Show | 77 | HG00280.hp2 HG00639.hp2 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.608-18076dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178859401 | |||||
| chr1:178859401
|
CTT | C | 31 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(28): Show | 31 | HG01099.hp1 HG01884.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.608-18077_608-1807 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178859401 | |||||
| chr1:178859401
|
CTTT | C | 30 | a0001c0002t0003g0013a0001c0002t0003g0015a0001c0002t0003g0016others(27): Show | 30 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.608-18078_608-1807 others(7): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178859401 | |||||
| chr1:178859404
|
T | C | 18 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(15): Show | 18 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.608-18094T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178859404 | ||||||
| chr1:178859463
|
T | G | 15 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(12): Show | 15 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.608-18035T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178859463 | ||||||
| chr1:178859472
|
C | T | 5 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.608-18026C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178859472 | ||||||
| chr1:178859695
|
C | CT | 71 | a0001c0001t0001g0057a0001c0001t0001g0160a0001c0001t0001g0162others(68): Show | 71 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.608-17782dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178859695 | |||||
| chr1:178859724
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.608-17774A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178859724 | ||||||
| chr1:178859732
|
T | C | 1 | a0001c0001t0002g0100 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.608-17766T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178859732 | ||||||
| chr1:178859738
|
G | A | 1 | a0001c0001t0001g0215 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.608-17760G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178859738 | ||||||
| chr1:178859743
|
G | C | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.608-17755G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178859743 | ||||||
| chr1:178859761
|
G | A | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.608-17737G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178859761 | ||||||
| chr1:178859820
|
G | C | 1 | a0001c0001t0001g0175 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.608-17678G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178859820 | ||||||
| chr1:178859820
|
G | GC | 106 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0056others(103): Show | 106 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.608-17665dupC | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178859820 | |||||
| chr1:178859820
|
G | GCC | 70 | a0001c0001t0001g0051a0001c0001t0001g0179a0001c0001t0001g0200others(67): Show | 70 | HG00280.hp2 HG00544.hp1 HG00642.hp1 others(67): Show |
intron_variant | MODIFIER | c.608-17666_608-1766 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178859820 | |||||
| chr1:178859820
|
G | GCCC | 18 | a0001c0001t0001g0132a0001c0001t0001g0170a0001c0001t0002g0099others(15): Show | 18 | HG00642.hp2 HG00738.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.608-17667_608-1766 others(7): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178859820 | |||||
| chr1:178859820
|
GC | G | 18 | a0001c0001t0001g0154a0001c0001t0001g0163a0001c0001t0001g0177others(15): Show | 18 | HG00280.hp1 HG01257.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.608-17665delC | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178859820 | |||||
| chr1:178859825
|
C | G | 15 | a0001c0001t0001g0053a0001c0001t0001g0060a0001c0001t0001g0145others(12): Show | 15 | HG00558.hp1 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.608-17673C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178859825 | ||||||
| chr1:178859829
|
C | CG | 3 | a0001c0001t0029g0156a0001c0002t0003g0024a0001c0002t0016g0030 | 3 | HG00423.hp1 HG02135.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.608-17669_608-1766 others(5): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178859829 | ||||||
| chr1:178859838
|
G | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.608-17660G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178859838 | ||||||
| chr1:178859866
|
G | A | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.608-17632G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178859866 | ||||||
| chr1:178859893
|
A | G | 2 | a0001c0001t0015g0108a0001c0001t0015g0109 | 2 | HG00280.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.608-17605A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178859893 | ||||||
| chr1:178859902
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.608-17596A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178859902 | ||||||
| chr1:178860120
|
C | G | 53 | a0001c0001t0001g0132a0001c0001t0002g0079a0001c0001t0002g0081others(50): Show | 53 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.608-17378C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178860120 | ||||||
| chr1:178860184
|
AT | A | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.608-17306delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178860184 | |||||
| chr1:178860255
|
TG | T | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.608-17242delG | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178860255 | ||||||
| chr1:178860258
|
A | T | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.608-17240A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178860258 | ||||||
| chr1:178860259
|
G | A | 149 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(146): Show | 149 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.608-17239G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178860259 | ||||||
| chr1:178860259
|
G | T | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.608-17239G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178860259 | ||||||
| chr1:178860260
|
C | A | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.608-17238C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178860260 | ||||||
| chr1:178860263
|
G | A | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.608-17235G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178860263 | ||||||
| chr1:178860264
|
T | TTA | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.608-17234_608-1723 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178860264 | ||||||
| chr1:178860272
|
A | G | 37 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(34): Show | 37 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.608-17226A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178860272 | ||||||
| chr1:178860290
|
AT | A | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.608-17204delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178860290 | |||||
| chr1:178860545
|
A | G | 6 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.608-16953A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178860545 | ||||||
| chr1:178860884
|
A | G | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.608-16614A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178860884 | ||||||
| chr1:178860956
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.608-16542G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178860956 | ||||||
| chr1:178860972
|
A | G | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.608-16526A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178860972 | ||||||
| chr1:178861260
|
A | C | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.608-16238A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178861260 | ||||||
| chr1:178861352
|
G | C | 1 | a0001c0001t0001g0302 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.608-16146G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178861352 | ||||||
| chr1:178861364
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.608-16134A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178861364 | ||||||
| chr1:178861450
|
G | GT | 9 | a0001c0001t0001g0194a0001c0001t0001g0249a0001c0001t0001g0276others(6): Show | 9 | HG00738.hp2 HG01099.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.608-16037dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178861450 | |||||
| chr1:178861467
|
A | G | 2 | a0001c0002t0023g0005a0001c0002t0023g0006 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.608-16031A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178861467 | ||||||
| chr1:178861493
|
A | G | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.608-16005A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178861493 | ||||||
| chr1:178861710
|
C | T | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.608-15788C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178861710 | ||||||
| chr1:178861768
|
A | G | 2 | a0001c0001t0006g0048a0001c0001t0006g0049 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.608-15730A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178861768 | ||||||
| chr1:178861958
|
C | T | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.608-15540C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178861958 | ||||||
| chr1:178862162
|
C | T | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.608-15336C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178862162 | ||||||
| chr1:178862337
|
G | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.608-15161G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178862337 | ||||||
| chr1:178862365
|
C | T | 1 | a0001c0001t0011g0257 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.608-15133C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178862365 | ||||||
| chr1:178862382
|
C | G | 2 | a0001c0001t0002g0002a0001c0001t0002g0003 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.608-15116C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178862382 | ||||||
| chr1:178862429
|
CTTAG | C | 12 | a0001c0002t0004g0012a0001c0002t0004g0120a0001c0002t0004g0121others(9): Show | 12 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.608-15064_608-1506 others(8): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178862429 | |||||
| chr1:178862588
|
ATTTT | A | 4 | a0001c0001t0001g0301a0001c0001t0002g0082a0001c0002t0005g0011others(1): Show | 4 | HG00733.hp1 HG01257.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.608-14905_608-1490 others(8): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178862588 | |||||
| chr1:178862589
|
T | TTTTA | 14 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0283others(11): Show | 14 | HG01099.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.608-14906_608-1490 others(8): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178862589 | |||||
| chr1:178862589
|
TTTTTTTT others(1): Show |
T | 4 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(1): Show | 4 | HG00738.hp2 HG02698.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.608-14905_608-1489 others(12): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178862589 | |||||
| chr1:178862589
|
TTTTTTTT others(5): Show |
T | 5 | a0001c0001t0010g0068a0001c0001t0010g0069a0001c0001t0010g0070others(2): Show | 5 | HG02486.hp2 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.608-14905_608-1489 others(16): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178862589 | |||||
| chr1:178862593
|
T | A | 26 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0283others(23): Show | 26 | HG01099.hp1 HG01884.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.608-14905T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178862593 | ||||||
| chr1:178862593
|
T | TTTTA | 51 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0157others(48): Show | 51 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.608-14869_608-1486 others(8): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178862593 | |||||
| chr1:178862593
|
T | TTTTATTT others(1): Show |
18 | a0001c0001t0001g0055a0001c0001t0001g0163a0001c0001t0001g0164others(15): Show | 18 | HG01361.hp1 HG02109.hp2 HG02523.hp2 others(15): Show |
intron_variant | MODIFIER | c.608-14873_608-1486 others(12): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178862593 | |||||
| chr1:178862593
|
T | TTTTATTT others(5): Show |
1 | a0001c0001t0001g0214 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.608-14877_608-1486 others(16): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178862593 | |||||
| chr1:178862593
|
TTTTA | T | 102 | a0001c0001t0001g0285a0001c0001t0002g0002a0001c0001t0002g0003others(99): Show | 102 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.608-14869_608-1486 others(8): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178862593 | |||||
| chr1:178862593
|
TTTTATTT others(1): Show |
T | 5 | a0001c0001t0001g0056a0001c0001t0001g0252a0001c0001t0001g0256others(2): Show | 5 | HG00438.hp2 HG00741.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.608-14873_608-1486 others(12): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178862593 | |||||
| chr1:178862593
|
TTTTATTT others(5): Show |
T | 11 | a0001c0001t0001g0216a0001c0001t0007g0064a0001c0001t0007g0065others(8): Show | 11 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.608-14877_608-1486 others(16): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178862593 | |||||
| chr1:178862601
|
A | T | 1 | a0001c0001t0001g0051 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.608-14897A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178862601 | ||||||
| chr1:178862630
|
TTTGG | T | 5 | a0001c0001t0006g0044a0001c0001t0006g0045a0001c0001t0006g0048others(2): Show | 5 | HG02280.hp1 HG02886.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.608-14849_608-1484 others(8): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178862630 | |||||
| chr1:178862633
|
G | A | 3 | a0001c0001t0006g0043a0001c0001t0006g0046a0001c0001t0006g0047 | 3 | HG01884.hp1 HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.608-14865G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178862633 | ||||||
| chr1:178862634
|
G | T | 3 | a0001c0001t0006g0043a0001c0001t0006g0046a0001c0001t0006g0047 | 3 | HG01884.hp1 HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.608-14864G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178862634 | ||||||
| chr1:178862688
|
A | G | 1 | a0001c0001t0007g0072 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.608-14810A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178862688 | ||||||
| chr1:178862729
|
G | A | 6 | a0001c0001t0002g0088a0001c0001t0002g0099a0001c0001t0002g0102others(3): Show | 6 | NA18941.hp2 NA18953.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.608-14769G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178862729 | ||||||
| chr1:178862767
|
C | T | 2 | a0001c0001t0002g0099a0001c0001t0002g0135 | 2 | NA18985.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.608-14731C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178862767 | ||||||
| chr1:178862806
|
T | C | 1 | a0001c0001t0015g0108 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.608-14692T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178862806 | ||||||
| chr1:178862955
|
A | G | 1 | a0001c0001t0002g0094 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.608-14543A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178862955 | ||||||
| chr1:178863190
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.608-14308A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178863190 | ||||||
| chr1:178863387
|
C | CAT | 148 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(145): Show | 148 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.608-14109_608-1410 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178863387 | |||||
| chr1:178863387
|
C | CGT | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.608-14111_608-1411 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178863387 | ||||||
| chr1:178863679
|
G | GT | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.608-13818dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178863679 | |||||
| chr1:178863783
|
A | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.608-13715A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178863783 | ||||||
| chr1:178863838
|
G | A | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.608-13660G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178863838 | ||||||
| chr1:178863875
|
A | G | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.608-13623A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178863875 | ||||||
| chr1:178863941
|
A | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.608-13557A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178863941 | ||||||
| chr1:178863995
|
C | T | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.608-13503C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178863995 | ||||||
| chr1:178864057
|
A | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.608-13441A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178864057 | ||||||
| chr1:178864303
|
A | C | 2 | a0001c0002t0023g0005a0001c0002t0023g0006 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.608-13195A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178864303 | ||||||
| chr1:178864321
|
A | G | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.608-13177A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178864321 | ||||||
| chr1:178864375
|
C | G | 151 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(148): Show | 151 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.608-13123C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178864375 | ||||||
| chr1:178864470
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.608-13028G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178864470 | ||||||
| chr1:178864596
|
G | T | 2 | a0001c0001t0002g0088a0001c0001t0002g0134 | 2 | NA18953.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.608-12902G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178864596 | ||||||
| chr1:178864731
|
T | G | 1 | a0001c0001t0002g0111 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.608-12767T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178864731 | ||||||
| chr1:178864739
|
C | T | 2 | a0001c0002t0003g0015a0001c0002t0003g0016 | 2 | NA18969.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.608-12759C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178864739 | ||||||
| chr1:178864767
|
T | G | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.608-12731T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178864767 | ||||||
| chr1:178864813
|
G | C | 1 | a0001c0002t0005g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.608-12685G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178864813 | ||||||
| chr1:178864860
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.608-12638G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178864860 | ||||||
| chr1:178864873
|
G | T | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.608-12625G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178864873 | ||||||
| chr1:178864977
|
G | A | 1 | a0001c0004t0004g0001 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.608-12521G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178864977 | ||||||
| chr1:178865012
|
C | T | 1 | a0001c0001t0006g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.608-12486C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178865012 | ||||||
| chr1:178865066
|
G | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.608-12432G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178865066 | ||||||
| chr1:178865096
|
T | C | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.608-12402T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178865096 | ||||||
| chr1:178865858
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.608-11640A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178865858 | ||||||
| chr1:178866212
|
T | A | 1 | a0001c0001t0001g0274 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.608-11286T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178866212 | ||||||
| chr1:178866485
|
T | C | 2 | a0001c0001t0001g0243a0001c0001t0001g0262 | 2 | NA18952.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.608-11013T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178866485 | ||||||
| chr1:178866749
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.608-10749G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178866749 | ||||||
| chr1:178866981
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.608-10517G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178866981 | ||||||
| chr1:178867187
|
G | A | 1 | a0001c0002t0003g0023 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.608-10311G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178867187 | ||||||
| chr1:178867226
|
A | G | 1 | a0001c0001t0016g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.608-10272A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178867226 | ||||||
| chr1:178867250
|
T | G | 2 | a0001c0001t0001g0256a0001c0001t0001g0301 | 2 | HG01257.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.608-10248T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178867250 | ||||||
| chr1:178867264
|
T | C | 1 | a0001c0001t0007g0067 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.608-10234T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178867264 | ||||||
| chr1:178867291
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.608-10207C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178867291 | ||||||
| chr1:178867313
|
C | A | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.608-10185C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178867313 | ||||||
| chr1:178867836
|
T | C | 57 | a0001c0001t0001g0132a0001c0001t0002g0002a0001c0001t0002g0003others(54): Show | 57 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.608-9662T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178867836 | ||||||
| chr1:178867988
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.608-9510A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178867988 | ||||||
| chr1:178868149
|
C | A | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.608-9349C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178868149 | ||||||
| chr1:178868209
|
G | A | 151 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(148): Show | 151 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.608-9289G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178868209 | ||||||
| chr1:178868476
|
A | C | 1 | a0001c0001t0014g0267 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.608-9022A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178868476 | ||||||
| chr1:178868501
|
A | G | 1 | a0001c0001t0032g0180 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.608-8997A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178868501 | ||||||
| chr1:178868547
|
A | G | 1 | a0001c0001t0001g0155 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.608-8951A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178868547 | ||||||
| chr1:178868729
|
A | C | 1 | a0001c0001t0013g0221 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.608-8769A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178868729 | ||||||
| chr1:178868744
|
T | C | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.608-8754T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178868744 | ||||||
| chr1:178868864
|
A | G | 4 | a0001c0001t0001g0176a0001c0001t0001g0196a0001c0001t0001g0197others(1): Show | 4 | HG00639.hp1 HG00733.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.608-8634A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178868864 | ||||||
| chr1:178868948
|
A | T | 1 | a0001c0001t0001g0252 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.608-8550A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178868948 | ||||||
| chr1:178869250
|
G | A | 33 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(30): Show | 33 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.608-8248G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178869250 | ||||||
| chr1:178869378
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.608-8120A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178869378 | ||||||
| chr1:178869487
|
C | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0191 | 2 | NA18941.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.608-8011C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178869487 | ||||||
| chr1:178869503
|
G | A | 1 | a0001c0001t0002g0107 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.608-7995G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178869503 | ||||||
| chr1:178869626
|
T | C | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.608-7872T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178869626 | ||||||
| chr1:178869627
|
A | G | 2 | a0001c0001t0002g0099a0001c0001t0002g0135 | 2 | NA18985.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.608-7871A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178869627 | ||||||
| chr1:178869679
|
A | G | 50 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(47): Show | 50 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.608-7819A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178869679 | ||||||
| chr1:178869686
|
A | G | 34 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(31): Show | 34 | HG00738.hp2 HG01099.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.608-7812A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178869686 | ||||||
| chr1:178869747
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.608-7751A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178869747 | ||||||
| chr1:178870341
|
G | A | 1 | a0001c0002t0003g0028 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.608-7157G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178870341 | ||||||
| chr1:178870494
|
A | G | 1 | a0001c0002t0005g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.608-7004A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178870494 | ||||||
| chr1:178871017
|
C | G | 1 | a0001c0001t0001g0182 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.608-6481C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178871017 | ||||||
| chr1:178871172
|
C | T | 1 | a0001c0002t0004g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.608-6326C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178871172 | ||||||
| chr1:178871175
|
T | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.608-6323T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178871175 | ||||||
| chr1:178871523
|
C | CTTAT | 211 | a0001c0001t0001g0056a0001c0001t0001g0132a0001c0001t0001g0155others(208): Show | 211 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.608-5974_608-5973i others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178871523 | |||||
| chr1:178871713
|
A | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.608-5785A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178871713 | ||||||
| chr1:178871765
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.608-5733G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178871765 | ||||||
| chr1:178871831
|
A | G | 1 | a0001c0001t0006g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.608-5667A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178871831 | ||||||
| chr1:178871860
|
C | T | 2 | a0001c0001t0001g0256a0001c0001t0001g0301 | 2 | HG01257.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.608-5638C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178871860 | ||||||
| chr1:178871941
|
A | G | 1 | a0001c0001t0001g0222 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.608-5557A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178871941 | ||||||
| chr1:178872152
|
C | T | 1 | a0001c0002t0005g0007 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.608-5346C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178872152 | ||||||
| chr1:178872393
|
G | A | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.608-5105G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178872393 | ||||||
| chr1:178872486
|
T | G | 1 | a0001c0001t0002g0100 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.608-5012T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178872486 | ||||||
| chr1:178872679
|
T | C | 1 | a0001c0001t0037g0077 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.608-4819T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178872679 | ||||||
| chr1:178872756
|
A | T | 1 | a0001c0001t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.608-4742A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178872756 | ||||||
| chr1:178872787
|
G | T | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.608-4711G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178872787 | ||||||
| chr1:178872837
|
T | C | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.608-4661T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178872837 | ||||||
| chr1:178872845
|
A | G | 46 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(43): Show | 46 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.608-4653A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178872845 | ||||||
| chr1:178873233
|
G | A | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.608-4265G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178873233 | ||||||
| chr1:178873379
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.608-4119C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178873379 | ||||||
| chr1:178873489
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.608-4009T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178873489 | ||||||
| chr1:178873667
|
C | T | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.608-3831C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178873667 | ||||||
| chr1:178873728
|
A | T | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.608-3770A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178873728 | ||||||
| chr1:178873743
|
T | G | 1 | a0001c0001t0028g0187 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.608-3755T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178873743 | ||||||
| chr1:178873748
|
T | C | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.608-3750T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178873748 | ||||||
| chr1:178873976
|
G | A | 2 | a0001c0001t0019g0146a0001c0001t0019g0147 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.608-3522G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178873976 | ||||||
| chr1:178874224
|
T | C | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.608-3274T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178874224 | ||||||
| chr1:178874315
|
A | G | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.608-3183A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178874315 | ||||||
| chr1:178874351
|
A | G | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.608-3147A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178874351 | ||||||
| chr1:178874435
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.608-3063G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178874435 | ||||||
| chr1:178874500
|
G | A | 1 | a0001c0001t0022g0059 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.608-2998G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178874500 | ||||||
| chr1:178874501
|
G | A | 1 | a0001c0001t0022g0059 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.608-2997G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178874501 | ||||||
| chr1:178874516
|
G | A | 9 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0002t0005g0007others(6): Show | 9 | HG00099.hp1 HG00597.hp1 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.608-2982G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178874516 | ||||||
| chr1:178874533
|
T | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.608-2965T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178874533 | ||||||
| chr1:178874611
|
C | T | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.608-2887C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178874611 | ||||||
| chr1:178874640
|
A | G | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.608-2858A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178874640 | ||||||
| chr1:178874711
|
G | A | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.608-2787G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178874711 | ||||||
| chr1:178874759
|
G | A | 150 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(147): Show | 150 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.608-2739G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178874759 | ||||||
| chr1:178874810
|
A | G | 2 | a0001c0001t0001g0228a0001c0001t0001g0234 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.608-2688A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178874810 | ||||||
| chr1:178874870
|
C | T | 3 | a0001c0002t0003g0013a0001c0002t0003g0029a0001c0002t0003g0032 | 3 | NA18959.hp1 NA19002.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.608-2628C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178874870 | ||||||
| chr1:178874896
|
A | G | 13 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.608-2602A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178874896 | ||||||
| chr1:178874906
|
G | A | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.608-2592G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178874906 | ||||||
| chr1:178874968
|
A | G | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.608-2530A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178874968 | ||||||
| chr1:178874998
|
A | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.608-2500A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178874998 | ||||||
| chr1:178875040
|
CAT | C | 13 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.608-2453_608-2452d others(4): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr1 | 178875040 | |||||
| chr1:178875374
|
A | G | 1 | a0001c0001t0037g0077 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.608-2124A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178875374 | ||||||
| chr1:178875479
|
G | A | 1 | a0001c0002t0005g0007 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.608-2019G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178875479 | ||||||
| chr1:178875564
|
A | G | 2 | a0001c0002t0023g0005a0001c0002t0023g0006 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.608-1934A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178875564 | ||||||
| chr1:178875703
|
G | A | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.608-1795G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178875703 | ||||||
| chr1:178875884
|
C | A | 1 | a0001c0001t0009g0144 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.608-1614C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178875884 | ||||||
| chr1:178875901
|
G | T | 10 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(7): Show | 10 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.608-1597G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178875901 | ||||||
| chr1:178876108
|
T | C | 2 | a0001c0001t0001g0212a0001c0001t0001g0222 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.608-1390T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178876108 | ||||||
| chr1:178876173
|
A | G | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.608-1325A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178876173 | ||||||
| chr1:178876288
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.608-1210A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178876288 | ||||||
| chr1:178876303
|
A | C | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.608-1195A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178876303 | ||||||
| chr1:178876344
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.608-1154G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178876344 | ||||||
| chr1:178876400
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.608-1098A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178876400 | ||||||
| chr1:178876497
|
T | G | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.608-1001T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178876497 | ||||||
| chr1:178877169
|
A | G | 4 | a0001c0001t0002g0088a0001c0001t0002g0102a0001c0001t0002g0134others(1): Show | 4 | NA18941.hp2 NA18953.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.608-329A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178877169 | ||||||
| chr1:178877294
|
A | G | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.608-204A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178877294 | ||||||
| chr1:178877374
|
G | A | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.608-124G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178877374 | ||||||
| chr1:178877975
|
C | T | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.745+340C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 9/19 | chr1 | 178877975 | ||||||
| chr1:178878135
|
C | G | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.745+500C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 9/19 | chr1 | 178878135 | ||||||
| chr1:178878138
|
G | A | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.745+503G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 9/19 | chr1 | 178878138 | ||||||
| chr1:178878224
|
AT | A | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.745+597delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr1 | 178878224 | |||||
| chr1:178878350
|
A | G | 2 | a0001c0001t0001g0230a0001c0001t0001g0254 | 2 | NA19057.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.746-552A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 9/19 | chr1 | 178878350 | ||||||
| chr1:178878713
|
A | G | 1 | a0001c0001t0013g0211 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.746-189A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 9/19 | chr1 | 178878713 | ||||||
| chr1:178879055
|
A | T | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.836+63A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178879055 | ||||||
| chr1:178879088
|
A | G | 46 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(43): Show | 46 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.836+96A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178879088 | ||||||
| chr1:178879273
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.836+281A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178879273 | ||||||
| chr1:178879470
|
C | T | 27 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(24): Show | 27 | HG01099.hp1 HG01884.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.836+478C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178879470 | ||||||
| chr1:178879531
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.836+539G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178879531 | ||||||
| chr1:178879558
|
C | T | 35 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(32): Show | 35 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.836+566C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178879558 | ||||||
| chr1:178879775
|
G | A | 37 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(34): Show | 37 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.836+783G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178879775 | ||||||
| chr1:178879784
|
C | T | 2 | a0001c0001t0019g0146a0001c0001t0019g0147 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.836+792C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178879784 | ||||||
| chr1:178879788
|
T | TA | 10 | a0001c0001t0001g0155a0001c0001t0001g0170a0001c0001t0001g0174others(7): Show | 10 | HG02280.hp2 HG02451.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.836+817dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr1 | 178879788 | |||||
| chr1:178879788
|
TA | T | 136 | a0001c0001t0001g0051a0001c0001t0001g0233a0001c0001t0001g0286others(133): Show | 136 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.836+817delA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr1 | 178879788 | |||||
| chr1:178879931
|
C | T | 27 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(24): Show | 27 | HG01099.hp1 HG01884.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.836+939C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178879931 | ||||||
| chr1:178880036
|
T | A | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.836+1044T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178880036 | ||||||
| chr1:178880046
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.836+1054A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178880046 | ||||||
| chr1:178880047
|
T | A | 1 | a0001c0001t0001g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.836+1055T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178880047 | ||||||
| chr1:178880048
|
T | A | 1 | a0001c0001t0001g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.836+1056T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178880048 | ||||||
| chr1:178880049
|
T | A | 1 | a0001c0001t0001g0212 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.836+1057T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178880049 | ||||||
| chr1:178880220
|
T | G | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.836+1228T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178880220 | ||||||
| chr1:178880236
|
T | G | 35 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(32): Show | 35 | HG00423.hp1 HG00544.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.836+1244T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178880236 | ||||||
| chr1:178880315
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.836+1323T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178880315 | ||||||
| chr1:178880354
|
G | A | 82 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(79): Show | 82 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.836+1362G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178880354 | ||||||
| chr1:178880396
|
A | G | 1 | a0001c0001t0002g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.836+1404A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178880396 | ||||||
| chr1:178880408
|
C | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.836+1416C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178880408 | ||||||
| chr1:178880481
|
A | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.836+1489A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178880481 | ||||||
| chr1:178880755
|
T | C | 1 | a0001c0001t0006g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.836+1763T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178880755 | ||||||
| chr1:178880769
|
A | G | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG01099.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.836+1777A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178880769 | ||||||
| chr1:178880913
|
T | A | 2 | a0001c0002t0003g0018a0001c0002t0003g0019 | 2 | NA19060.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.836+1921T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178880913 | ||||||
| chr1:178881251
|
A | G | 1 | a0001c0001t0002g0082 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.837-2215A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178881251 | ||||||
| chr1:178881367
|
A | C | 1 | a0002c0005t0039g0042 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.837-2099A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178881367 | ||||||
| chr1:178881400
|
C | T | 2 | a0001c0001t0014g0267a0001c0001t0014g0268 | 2 | NA18747.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.837-2066C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178881400 | ||||||
| chr1:178881454
|
T | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.837-2012T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178881454 | ||||||
| chr1:178881581
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.837-1885G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178881581 | ||||||
| chr1:178881609
|
C | T | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.837-1857C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178881609 | ||||||
| chr1:178881702
|
T | C | 81 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(78): Show | 81 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.837-1764T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178881702 | ||||||
| chr1:178881741
|
G | A | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.837-1725G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178881741 | ||||||
| chr1:178881903
|
G | A | 1 | a0001c0001t0006g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.837-1563G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178881903 | ||||||
| chr1:178882045
|
A | G | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.837-1421A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178882045 | ||||||
| chr1:178882070
|
C | A | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.837-1396C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178882070 | ||||||
| chr1:178882197
|
TGATTCAC others(7): Show |
T | 45 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(42): Show | 45 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.837-1267_837-1254d others(16): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr1 | 178882197 | |||||
| chr1:178882322
|
G | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0254 | 2 | NA19057.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.837-1144G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178882322 | ||||||
| chr1:178882444
|
C | G | 1 | a0001c0001t0002g0289 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.837-1022C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178882444 | ||||||
| chr1:178882905
|
T | C | 3 | a0001c0001t0002g0095a0001c0001t0002g0097a0001c0001t0002g0098 | 3 | NA18959.hp2 NA18983.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.837-561T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178882905 | ||||||
| chr1:178883011
|
C | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.837-455C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178883011 | ||||||
| chr1:178883031
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.837-435A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178883031 | ||||||
| chr1:178883043
|
G | A | 2 | a0001c0002t0004g0012a0001c0002t0004g0129 | 2 | HG02109.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.837-423G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178883043 | ||||||
| chr1:178883197
|
T | C | 1 | a0001c0001t0006g0043 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.837-269T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178883197 | ||||||
| chr1:178883313
|
A | AT | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.837-153_837-152ins others(1): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 10/19 | chr1 | 178883313 | ||||||
| chr1:178883616
|
T | A | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.904+83T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 11/19 | chr1 | 178883616 | ||||||
| chr1:178883665
|
T | A | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.904+132T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 11/19 | chr1 | 178883665 | ||||||
| chr1:178883708
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.904+175G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 11/19 | chr1 | 178883708 | ||||||
| chr1:178883858
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.904+325G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 11/19 | chr1 | 178883858 | ||||||
| chr1:178883938
|
G | A | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.904+405G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 11/19 | chr1 | 178883938 | ||||||
| chr1:178884286
|
C | T | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.904+753C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 11/19 | chr1 | 178884286 | ||||||
| chr1:178884436
|
A | G | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.905-640A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 11/19 | chr1 | 178884436 | ||||||
| chr1:178884474
|
T | TAAA | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-602_905-601ins others(3): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 11/19 | chr1 | 178884474 | ||||||
| chr1:178884474
|
T | TGAA | 256 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.905-600_905-598dup others(3): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr1 | 178884474 | |||||
| chr1:178884521
|
C | G | 1 | a0001c0001t0001g0223 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.905-555C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 11/19 | chr1 | 178884521 | ||||||
| chr1:178884786
|
A | G | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.905-290A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 11/19 | chr1 | 178884786 | ||||||
| chr1:178884914
|
G | T | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.905-162G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 11/19 | chr1 | 178884914 | ||||||
| chr1:178885027
|
C | T | 201 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(198): Show | 201 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.905-49C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 11/19 | chr1 | 178885027 | ||||||
| chr1:178885285
|
A | G | 9 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(6): Show | 9 | HG01069.hp1 HG01884.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1040+74A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 12/19 | chr1 | 178885285 | ||||||
| chr1:178885634
|
T | C | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.1041-335T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 12/19 | chr1 | 178885634 | ||||||
| chr1:178885774
|
G | A | 2 | a0001c0001t0001g0197a0001c0001t0027g0172 | 2 | HG00733.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1041-195G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 12/19 | chr1 | 178885774 | ||||||
| chr1:178885829
|
A | G | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG01099.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1041-140A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 12/19 | chr1 | 178885829 | ||||||
| chr1:178886347
|
G | A | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1192+227G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178886347 | ||||||
| chr1:178886390
|
G | A | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1192+270G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178886390 | ||||||
| chr1:178886512
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1192+392G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178886512 | ||||||
| chr1:178886558
|
C | G | 5 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1192+438C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178886558 | ||||||
| chr1:178886764
|
A | G | 1 | a0001c0001t0009g0144 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1192+644A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178886764 | ||||||
| chr1:178886805
|
C | T | 1 | a0001c0002t0003g0021 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1192+685C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178886805 | ||||||
| chr1:178886845
|
A | G | 1 | a0001c0001t0016g0184 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1192+725A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178886845 | ||||||
| chr1:178886855
|
A | G | 2 | a0001c0002t0003g0018a0001c0002t0003g0019 | 2 | NA19060.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1192+735A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178886855 | ||||||
| chr1:178887071
|
A | G | 1 | a0001c0001t0002g0095 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1192+951A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178887071 | ||||||
| chr1:178887102
|
C | T | 1 | a0001c0001t0002g0079 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1192+982C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178887102 | ||||||
| chr1:178887218
|
C | T | 2 | a0001c0001t0001g0228a0001c0001t0001g0234 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1192+1098C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178887218 | ||||||
| chr1:178887299
|
A | C | 1 | a0001c0001t0002g0288 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1192+1179A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178887299 | ||||||
| chr1:178887442
|
G | A | 1 | a0001c0002t0004g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1192+1322G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178887442 | ||||||
| chr1:178887600
|
C | T | 3 | a0001c0001t0019g0146a0001c0001t0019g0147a0001c0001t0036g0137 | 3 | HG02486.hp2 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1192+1480C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178887600 | ||||||
| chr1:178887870
|
A | G | 305 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.1192+1750A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178887870 | ||||||
| chr1:178888013
|
T | G | 1 | a0001c0001t0002g0079 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1193-1629T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178888013 | ||||||
| chr1:178888014
|
G | T | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1193-1628G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178888014 | ||||||
| chr1:178888052
|
G | A | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1193-1590G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178888052 | ||||||
| chr1:178888052
|
G | T | 1 | a0001c0001t0001g0274 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1193-1590G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178888052 | ||||||
| chr1:178888383
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1193-1259G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178888383 | ||||||
| chr1:178888538
|
A | T | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1193-1104A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178888538 | ||||||
| chr1:178888548
|
T | A | 13 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1193-1094T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178888548 | ||||||
| chr1:178888563
|
A | C | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1193-1079A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178888563 | ||||||
| chr1:178888618
|
A | T | 3 | a0001c0001t0002g0089a0001c0001t0002g0100a0001c0001t0002g0136 | 3 | NA18974.hp1 NA19012.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1193-1024A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178888618 | ||||||
| chr1:178888669
|
A | G | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1193-973A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178888669 | ||||||
| chr1:178888779
|
C | T | 2 | a0001c0001t0010g0062a0001c0001t0010g0063 | 2 | HG02630.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1193-863C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178888779 | ||||||
| chr1:178888810
|
A | G | 1 | a0001c0001t0001g0298 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1193-832A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178888810 | ||||||
| chr1:178889022
|
C | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1193-620C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178889022 | ||||||
| chr1:178889134
|
A | T | 1 | a0001c0002t0003g0025 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1193-508A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178889134 | ||||||
| chr1:178889442
|
C | T | 1 | a0001c0001t0002g0103 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1193-200C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178889442 | ||||||
| chr1:178889489
|
A | T | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1193-153A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178889489 | ||||||
| chr1:178889576
|
C | A | 155 | a0001c0001t0001g0056a0001c0001t0001g0252a0001c0001t0001g0256others(152): Show | 155 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.1193-66C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178889576 | ||||||
| chr1:178889624
|
G | A | 155 | a0001c0001t0001g0056a0001c0001t0001g0252a0001c0001t0001g0256others(152): Show | 155 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.1193-18G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 13/19 | chr1 | 178889624 | ||||||
| chr1:178889720
|
C | T | 1 | a0001c0001t0006g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1247+24C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 14/19 | chr1 | 178889720 | ||||||
| chr1:178889756
|
A | G | 1 | a0001c0001t0002g0289 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1247+60A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 14/19 | chr1 | 178889756 | ||||||
| chr1:178889949
|
TAAAA | T | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1247+255_1247+258d others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr1 | 178889949 | |||||
| chr1:178889988
|
A | G | 10 | a0001c0002t0004g0120a0001c0002t0004g0121a0001c0002t0004g0122others(7): Show | 10 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.1247+292A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 14/19 | chr1 | 178889988 | ||||||
| chr1:178890009
|
T | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1247+313T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 14/19 | chr1 | 178890009 | ||||||
| chr1:178890134
|
T | C | 6 | a0001c0001t0006g0048a0001c0001t0006g0049a0001c0001t0006g0050others(3): Show | 6 | HG02280.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1247+438T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 14/19 | chr1 | 178890134 | ||||||
| chr1:178890468
|
G | A | 305 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.1247+772G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 14/19 | chr1 | 178890468 | ||||||
| chr1:178890476
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1247+780C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 14/19 | chr1 | 178890476 | ||||||
| chr1:178890613
|
T | C | 2 | a0001c0001t0002g0099a0001c0001t0002g0135 | 2 | NA18985.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.1247+917T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 14/19 | chr1 | 178890613 | ||||||
| chr1:178891095
|
A | G | 6 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1248-1135A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 14/19 | chr1 | 178891095 | ||||||
| chr1:178891495
|
T | A | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1248-735T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 14/19 | chr1 | 178891495 | ||||||
| chr1:178891602
|
TA | T | 6 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1248-627delA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 14/19 | chr1 | 178891602 | ||||||
| chr1:178891665
|
A | G | 3 | a0001c0001t0001g0223a0001c0001t0001g0238a0001c0001t0001g0239 | 3 | NA18939.hp2 NA18953.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1248-565A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 14/19 | chr1 | 178891665 | ||||||
| chr1:178891890
|
G | A | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1248-340G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 14/19 | chr1 | 178891890 | ||||||
| chr1:178891916
|
GT | G | 156 | a0001c0001t0001g0056a0001c0001t0001g0252a0001c0001t0001g0256others(153): Show | 156 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.1248-304delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr1 | 178891916 | |||||
| chr1:178892143
|
G | T | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.1248-87G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 14/19 | chr1 | 178892143 | ||||||
| chr1:178892378
|
G | A | 1 | a0001c0001t0002g0290 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1325+71G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | chr1 | 178892378 | ||||||
| chr1:178892611
|
A | G | 2 | a0001c0001t0002g0002a0001c0001t0002g0003 | 2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1325+304A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | chr1 | 178892611 | ||||||
| chr1:178892635
|
A | G | 18 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0055others(15): Show | 18 | HG00099.hp2 HG00438.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.1325+328A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | chr1 | 178892635 | ||||||
| chr1:178892778
|
C | T | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1325+471C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | chr1 | 178892778 | ||||||
| chr1:178892857
|
A | T | 49 | a0001c0001t0001g0056a0001c0001t0001g0252a0001c0001t0001g0256others(46): Show | 49 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1325+550A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | chr1 | 178892857 | ||||||
| chr1:178893016
|
A | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1325+709A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | chr1 | 178893016 | ||||||
| chr1:178893209
|
A | G | 1 | a0001c0001t0002g0153 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1326-710A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | chr1 | 178893209 | ||||||
| chr1:178893213
|
G | C | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1326-706G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | chr1 | 178893213 | ||||||
| chr1:178893245
|
A | AT | 85 | a0001c0001t0001g0056a0001c0001t0001g0145a0001c0001t0001g0252others(82): Show | 85 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.1326-661dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 178893245 | |||||
| chr1:178893259
|
A | T | 5 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1326-660A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | chr1 | 178893259 | ||||||
| chr1:178893269
|
T | C | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1326-650T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | chr1 | 178893269 | ||||||
| chr1:178893294
|
T | C | 1 | a0001c0001t0002g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1326-625T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | chr1 | 178893294 | ||||||
| chr1:178893306
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1326-613G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | chr1 | 178893306 | ||||||
| chr1:178893452
|
TC | T | 3 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0217 | 3 | HG01070.hp1 HG01261.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1326-466delC | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | chr1 | 178893452 | ||||||
| chr1:178893453
|
C | CT | 14 | a0001c0001t0001g0198a0001c0001t0001g0258a0001c0001t0001g0276others(11): Show | 14 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1326-453dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 178893453 | |||||
| chr1:178893453
|
CT | C | 6 | a0001c0001t0001g0300a0001c0001t0001g0301a0001c0001t0002g0105others(3): Show | 6 | HG00438.hp1 HG01257.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.1326-453delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr1 | 178893453 | |||||
| chr1:178893512
|
T | C | 1 | a0001c0001t0002g0131 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1326-407T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | chr1 | 178893512 | ||||||
| chr1:178893635
|
A | T | 1 | a0001c0001t0001g0229 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1326-284A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | chr1 | 178893635 | ||||||
| chr1:178893644
|
A | G | 9 | a0001c0001t0002g0110a0001c0001t0002g0288a0001c0001t0002g0296others(6): Show | 9 | HG00738.hp2 HG01074.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.1326-275A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | chr1 | 178893644 | ||||||
| chr1:178893662
|
C | T | 44 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(41): Show | 44 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.1326-257C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | chr1 | 178893662 | ||||||
| chr1:178893888
|
C | T | 14 | a0001c0001t0001g0060a0001c0001t0001g0206a0001c0001t0001g0209others(11): Show | 14 | HG01106.hp1 HG01255.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.1326-31C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 15/19 | chr1 | 178893888 | ||||||
| chr1:178894131
|
C | T | 49 | a0001c0001t0001g0056a0001c0001t0001g0252a0001c0001t0001g0256others(46): Show | 49 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1431+107C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178894131 | ||||||
| chr1:178894199
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1431+175A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178894199 | ||||||
| chr1:178894271
|
T | C | 23 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(20): Show | 23 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(20): Show |
intron_variant | MODIFIER | c.1431+247T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178894271 | ||||||
| chr1:178894311
|
A | G | 2 | a0001c0001t0002g0078a0001c0001t0037g0077 | 2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1431+287A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178894311 | ||||||
| chr1:178894448
|
T | C | 1 | a0001c0001t0001g0274 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1431+424T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178894448 | ||||||
| chr1:178894461
|
T | C | 27 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(24): Show | 27 | HG01099.hp1 HG01884.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1431+437T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178894461 | ||||||
| chr1:178894713
|
G | C | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1431+689G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178894713 | ||||||
| chr1:178894782
|
T | C | 1 | a0001c0001t0002g0115 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1431+758T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178894782 | ||||||
| chr1:178894825
|
A | G | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1431+801A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178894825 | ||||||
| chr1:178894999
|
T | C | 3 | a0001c0001t0007g0067a0001c0001t0007g0071a0001c0001t0007g0073 | 3 | HG01346.hp2 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1431+975T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178894999 | ||||||
| chr1:178895064
|
T | C | 6 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1431+1040T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178895064 | ||||||
| chr1:178895109
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1431+1085T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178895109 | ||||||
| chr1:178895143
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1431+1119C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178895143 | ||||||
| chr1:178895466
|
A | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1431+1442A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178895466 | ||||||
| chr1:178895568
|
C | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1431+1544C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178895568 | ||||||
| chr1:178895617
|
G | A | 2 | a0001c0001t0001g0251a0001c0002t0005g0130 | 2 | HG03225.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1431+1593G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178895617 | ||||||
| chr1:178895805
|
A | C | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1431+1781A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178895805 | ||||||
| chr1:178895964
|
T | C | 1 | a0001c0002t0025g0149 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1432-1700T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178895964 | ||||||
| chr1:178896160
|
T | C | 151 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(148): Show | 151 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.1432-1504T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178896160 | ||||||
| chr1:178896456
|
AT | A | 17 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(14): Show | 17 | HG00738.hp2 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1432-1198delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 178896456 | |||||
| chr1:178896466
|
T | C | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1432-1198T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178896466 | ||||||
| chr1:178896467
|
C | T | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1432-1197C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178896467 | ||||||
| chr1:178896467
|
CT | C | 17 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(14): Show | 17 | HG01346.hp2 HG02257.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1432-1184delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 178896467 | |||||
| chr1:178896468
|
T | C | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1432-1196T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178896468 | ||||||
| chr1:178896499
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1432-1165G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178896499 | ||||||
| chr1:178896509
|
G | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1432-1155G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178896509 | ||||||
| chr1:178896514
|
T | A | 3 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045 | 3 | HG02886.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1432-1150T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178896514 | ||||||
| chr1:178896611
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1432-1053C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178896611 | ||||||
| chr1:178896677
|
G | A | 13 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1432-987G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178896677 | ||||||
| chr1:178896682
|
A | G | 3 | a0001c0001t0019g0146a0001c0001t0019g0147a0001c0001t0036g0137 | 3 | HG02486.hp2 HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1432-982A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178896682 | ||||||
| chr1:178896876
|
A | G | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1432-788A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178896876 | ||||||
| chr1:178896910
|
C | T | 2 | a0001c0001t0014g0275a0001c0001t0029g0156 | 2 | HG00544.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1432-754C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178896910 | ||||||
| chr1:178896960
|
C | G | 1 | a0001c0001t0001g0283 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1432-704C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178896960 | ||||||
| chr1:178896966
|
T | G | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1432-698T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178896966 | ||||||
| chr1:178897123
|
G | A | 1 | a0001c0002t0004g0012 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1432-541G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178897123 | ||||||
| chr1:178897177
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1432-487C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178897177 | ||||||
| chr1:178897539
|
A | G | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1432-125A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178897539 | ||||||
| chr1:178897567
|
T | A | 1 | a0001c0001t0038g0292 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1432-97T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178897567 | ||||||
| chr1:178897580
|
A | G | 1 | a0001c0001t0002g0133 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1432-84A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178897580 | ||||||
| chr1:178897612
|
C | CT | 5 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1432-51dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | INFO_REALIGN_3_PRIME | chr1 | 178897612 | |||||
| chr1:178897626
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0189 | 2 | HG01952.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1432-38G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 16/19 | chr1 | 178897626 | ||||||
| chr1:178897963
|
G | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1524+207G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178897963 | ||||||
| chr1:178898122
|
G | C | 2 | a0001c0001t0019g0146a0001c0001t0019g0147 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1524+366G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178898122 | ||||||
| chr1:178898154
|
A | C | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1524+398A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178898154 | ||||||
| chr1:178898155
|
A | G | 10 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(7): Show | 10 | HG00738.hp2 HG01099.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1524+399A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178898155 | ||||||
| chr1:178898233
|
T | C | 1 | a0001c0002t0016g0030 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1524+477T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178898233 | ||||||
| chr1:178898819
|
C | T | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1524+1063C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178898819 | ||||||
| chr1:178899117
|
A | G | 1 | a0001c0001t0001g0194 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1524+1361A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178899117 | ||||||
| chr1:178899319
|
C | A | 4 | a0001c0001t0001g0176a0001c0001t0001g0196a0001c0001t0001g0197others(1): Show | 4 | HG00639.hp1 HG00733.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+1563C>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178899319 | ||||||
| chr1:178899344
|
C | T | 1 | a0001c0001t0006g0047 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1524+1588C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178899344 | ||||||
| chr1:178899468
|
T | C | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1524+1712T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178899468 | ||||||
| chr1:178899504
|
G | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1524+1748G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178899504 | ||||||
| chr1:178899573
|
G | T | 1 | a0001c0001t0002g0153 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1524+1817G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178899573 | ||||||
| chr1:178899616
|
T | TGTTTTG | 11 | a0001c0001t0001g0055a0001c0001t0001g0186a0001c0001t0001g0225others(8): Show | 11 | HG04228.hp1 NA18522.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.1524+1896_1524+190 others(10): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr1 | 178899616 | |||||
| chr1:178899616
|
TGTTTTGG others(5): Show |
T | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1524+1890_1524+190 others(16): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr1 | 178899616 | |||||
| chr1:178899622
|
G | T | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+1866G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178899622 | ||||||
| chr1:178899645
|
TG | T | 10 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(7): Show | 10 | HG01099.hp1 HG01884.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+1891delG | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr1 | 178899645 | |||||
| chr1:178899647
|
G | GT | 16 | a0001c0002t0003g0013a0001c0002t0003g0031a0001c0002t0004g0012others(13): Show | 16 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1524+1895dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr1 | 178899647 | |||||
| chr1:178899647
|
G | T | 17 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(14): Show | 17 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1524+1891G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178899647 | ||||||
| chr1:178899651
|
TG | T | 3 | a0001c0001t0012g0039a0001c0001t0012g0041a0001c0001t0021g0075 | 3 | HG00738.hp2 HG02895.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1524+1897delG | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr1 | 178899651 | |||||
| chr1:178899652
|
G | T | 68 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(65): Show | 68 | HG00544.hp1 HG00642.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.1524+1896G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178899652 | ||||||
| chr1:178899653
|
G | GTTTTTT | 7 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(4): Show | 7 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1524+1903_1524+190 others(10): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr1 | 178899653 | |||||
| chr1:178899653
|
G | T | 58 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(55): Show | 58 | HG00544.hp1 HG00642.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.1524+1897G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178899653 | ||||||
| chr1:178899653
|
GT | G | 13 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1524+1908delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr1 | 178899653 | |||||
| chr1:178899654
|
T | G | 1 | a0001c0001t0001g0197 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1524+1898T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178899654 | ||||||
| chr1:178899664
|
T | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1524+1908T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178899664 | ||||||
| chr1:178900219
|
A | G | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1525-1887A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178900219 | ||||||
| chr1:178900353
|
A | T | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1525-1753A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178900353 | ||||||
| chr1:178900483
|
T | G | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1525-1623T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178900483 | ||||||
| chr1:178900612
|
T | G | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1525-1494T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178900612 | ||||||
| chr1:178900767
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1525-1339T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178900767 | ||||||
| chr1:178900781
|
G | T | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1525-1325G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178900781 | ||||||
| chr1:178900830
|
C | T | 1 | a0001c0001t0002g0289 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1525-1276C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178900830 | ||||||
| chr1:178900947
|
T | C | 13 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1525-1159T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178900947 | ||||||
| chr1:178901111
|
G | A | 13 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1525-995G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178901111 | ||||||
| chr1:178901381
|
C | T | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1525-725C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178901381 | ||||||
| chr1:178901420
|
C | G | 43 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(40): Show | 43 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1525-686C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178901420 | ||||||
| chr1:178901543
|
C | G | 13 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1525-563C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178901543 | ||||||
| chr1:178901685
|
C | CA | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG01099.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1525-407dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr1 | 178901685 | |||||
| chr1:178901723
|
T | C | 5 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076others(2): Show | 5 | HG02895.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-383T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178901723 | ||||||
| chr1:178901773
|
C | T | 5 | a0001c0001t0006g0046a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1525-333C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178901773 | ||||||
| chr1:178902082
|
G | A | 81 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(78): Show | 81 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1525-24G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 17/19 | chr1 | 178902082 | ||||||
| chr1:178902676
|
A | T | 1 | a0001c0001t0001g0210 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1630+465A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178902676 | ||||||
| chr1:178902720
|
A | G | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1630+509A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178902720 | ||||||
| chr1:178902754
|
G | A | 43 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(40): Show | 43 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1630+543G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178902754 | ||||||
| chr1:178903074
|
T | G | 1 | a0001c0001t0001g0054 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1630+863T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178903074 | ||||||
| chr1:178903170
|
A | G | 3 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045 | 3 | HG02886.hp2 HG06807.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1630+959A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178903170 | ||||||
| chr1:178903299
|
T | C | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1630+1088T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178903299 | ||||||
| chr1:178903332
|
A | G | 3 | a0001c0001t0001g0195a0001c0001t0001g0220a0001c0001t0001g0227 | 3 | HG01106.hp2 HG01256.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1630+1121A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178903332 | ||||||
| chr1:178903424
|
T | C | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1630+1213T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178903424 | ||||||
| chr1:178903452
|
C | T | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1630+1241C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178903452 | ||||||
| chr1:178903580
|
G | A | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1630+1369G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178903580 | ||||||
| chr1:178903644
|
T | C | 201 | a0001c0001t0001g0056a0001c0001t0001g0155a0001c0001t0001g0158others(198): Show | 201 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.1630+1433T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178903644 | ||||||
| chr1:178903743
|
C | T | 36 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(33): Show | 36 | HG00544.hp1 HG00642.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.1630+1532C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178903743 | ||||||
| chr1:178903748
|
T | C | 1 | a0001c0001t0011g0240 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1630+1537T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178903748 | ||||||
| chr1:178903901
|
CT | C | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1630+1694delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr1 | 178903901 | |||||
| chr1:178903946
|
G | A | 1 | a0001c0001t0002g0290 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1630+1735G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178903946 | ||||||
| chr1:178904062
|
G | C | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1630+1851G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178904062 | ||||||
| chr1:178904453
|
A | G | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1630+2242A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178904453 | ||||||
| chr1:178904464
|
T | G | 3 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041 | 3 | HG00738.hp2 HG02698.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1630+2253T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178904464 | ||||||
| chr1:178904492
|
T | C | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1630+2281T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178904492 | ||||||
| chr1:178904617
|
C | T | 6 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1631-2159C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178904617 | ||||||
| chr1:178904637
|
C | T | 29 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0154others(26): Show | 29 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.1631-2139C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178904637 | ||||||
| chr1:178904686
|
A | C | 2 | a0001c0002t0023g0005a0001c0002t0023g0006 | 2 | HG02922.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1631-2090A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178904686 | ||||||
| chr1:178904755
|
C | T | 5 | a0001c0001t0006g0046a0001c0001t0006g0047a0001c0001t0006g0048others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1631-2021C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178904755 | ||||||
| chr1:178904873
|
G | A | 150 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(147): Show | 150 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.1631-1903G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178904873 | ||||||
| chr1:178904897
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1631-1879A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178904897 | ||||||
| chr1:178905236
|
A | G | 1 | a0001c0001t0040g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1631-1540A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178905236 | ||||||
| chr1:178905260
|
T | C | 31 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(28): Show | 31 | HG00738.hp2 HG01099.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1631-1516T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178905260 | ||||||
| chr1:178905367
|
C | CTA | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1631-1406_1631-140 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr1 | 178905367 | |||||
| chr1:178905377
|
G | C | 1 | a0001c0001t0029g0156 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1631-1399G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178905377 | ||||||
| chr1:178905492
|
G | A | 81 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(78): Show | 81 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.1631-1284G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178905492 | ||||||
| chr1:178905772
|
T | C | 1 | a0001c0001t0001g0201 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1631-1004T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178905772 | ||||||
| chr1:178905803
|
G | A | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1631-973G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178905803 | ||||||
| chr1:178905893
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1631-883A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178905893 | ||||||
| chr1:178905918
|
A | G | 3 | a0001c0001t0014g0267a0001c0001t0014g0268a0001c0001t0014g0275 | 3 | HG00544.hp2 NA18747.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1631-858A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178905918 | ||||||
| chr1:178906132
|
G | A | 1 | a0001c0001t0022g0059 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1631-644G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178906132 | ||||||
| chr1:178906374
|
C | CA | 8 | a0001c0001t0002g0131a0001c0001t0009g0138a0001c0001t0009g0140others(5): Show | 8 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1631-389dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr1 | 178906374 | |||||
| chr1:178906374
|
C | CAAA | 6 | a0001c0001t0008g0112a0001c0001t0008g0113a0001c0001t0008g0114others(3): Show | 6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1631-391_1631-389d others(5): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr1 | 178906374 | |||||
| chr1:178906443
|
T | G | 1 | a0001c0002t0016g0030 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1631-333T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178906443 | ||||||
| chr1:178906446
|
C | G | 1 | a0001c0002t0016g0030 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1631-330C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 18/19 | chr1 | 178906446 | ||||||
| chr1:178906919
|
A | G | 11 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(8): Show | 11 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.1722+52A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178906919 | ||||||
| chr1:178906949
|
G | C | 1 | a0001c0001t0011g0260 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1722+82G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178906949 | ||||||
| chr1:178907224
|
A | G | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1722+357A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178907224 | ||||||
| chr1:178907390
|
C | T | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.1722+523C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178907390 | ||||||
| chr1:178907434
|
C | T | 1 | a0001c0001t0006g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1722+567C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178907434 | ||||||
| chr1:178907447
|
G | A | 5 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0092others(2): Show | 5 | HG00741.hp2 HG01261.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1722+580G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178907447 | ||||||
| chr1:178907475
|
G | A | 1 | a0001c0001t0010g0068 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1722+608G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178907475 | ||||||
| chr1:178907622
|
A | G | 8 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(5): Show | 8 | HG00738.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1722+755A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178907622 | ||||||
| chr1:178907709
|
G | A | 22 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(19): Show | 22 | HG00544.hp1 HG00642.hp2 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.1722+842G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178907709 | ||||||
| chr1:178907757
|
C | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1722+890C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178907757 | ||||||
| chr1:178907779
|
T | C | 22 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(19): Show | 22 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1722+912T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178907779 | ||||||
| chr1:178907785
|
A | G | 22 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(19): Show | 22 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1722+918A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178907785 | ||||||
| chr1:178907858
|
T | C | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1722+991T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178907858 | ||||||
| chr1:178907866
|
G | T | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1722+999G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178907866 | ||||||
| chr1:178907976
|
A | G | 1 | a0001c0004t0004g0001 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1722+1109A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178907976 | ||||||
| chr1:178908118
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1722+1251G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178908118 | ||||||
| chr1:178908347
|
G | A | 9 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(6): Show | 9 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1722+1480G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178908347 | ||||||
| chr1:178908372
|
T | A | 1 | a0001c0001t0001g0200 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1722+1505T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178908372 | ||||||
| chr1:178908677
|
C | T | 1 | a0001c0001t0002g0116 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1722+1810C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178908677 | ||||||
| chr1:178908997
|
G | T | 1 | a0001c0001t0036g0137 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1722+2130G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178908997 | ||||||
| chr1:178909083
|
C | G | 1 | a0001c0001t0002g0134 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1722+2216C>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178909083 | ||||||
| chr1:178909084
|
A | T | 1 | a0001c0001t0002g0134 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1722+2217A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178909084 | ||||||
| chr1:178909140
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1722+2273G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178909140 | ||||||
| chr1:178909294
|
A | G | 1 | a0001c0001t0002g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1722+2427A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178909294 | ||||||
| chr1:178909343
|
G | A | 2 | a0001c0001t0019g0146a0001c0001t0019g0147 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1722+2476G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178909343 | ||||||
| chr1:178909420
|
TGTTGTTG others(3): Show |
T | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1722+2554_1722+256 others(14): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178909420 | ||||||
| chr1:178909445
|
T | G | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1722+2578T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178909445 | ||||||
| chr1:178909456
|
T | G | 1 | a0001c0002t0004g0129 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1722+2589T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178909456 | ||||||
| chr1:178909484
|
G | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1722+2617G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178909484 | ||||||
| chr1:178909498
|
G | A | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1722+2631G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178909498 | ||||||
| chr1:178909557
|
A | C | 1 | a0001c0001t0011g0240 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1722+2690A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178909557 | ||||||
| chr1:178909643
|
A | AT | 28 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0058others(25): Show | 28 | HG00423.hp2 HG00639.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1722+2800dupT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 178909643 | |||||
| chr1:178909643
|
AT | A | 99 | a0001c0001t0001g0055a0001c0001t0001g0159a0001c0001t0001g0224others(96): Show | 99 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.1722+2800delT | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 178909643 | |||||
| chr1:178909643
|
ATT | A | 43 | a0001c0001t0002g0135a0001c0001t0008g0112a0001c0001t0008g0113others(40): Show | 43 | HG00544.hp1 HG00642.hp2 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.1722+2799_1722+280 others(6): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 178909643 | |||||
| chr1:178909684
|
T | A | 21 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(18): Show | 21 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1722+2817T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178909684 | ||||||
| chr1:178909712
|
C | T | 7 | a0001c0002t0005g0007a0001c0002t0005g0008a0001c0002t0005g0009others(4): Show | 7 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1722+2845C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178909712 | ||||||
| chr1:178909753
|
G | A | 2 | a0001c0001t0001g0228a0001c0001t0001g0234 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1722+2886G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178909753 | ||||||
| chr1:178909835
|
G | A | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1722+2968G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178909835 | ||||||
| chr1:178909901
|
C | T | 45 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(42): Show | 45 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.1722+3034C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178909901 | ||||||
| chr1:178909922
|
T | G | 56 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0078others(53): Show | 56 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1722+3055T>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178909922 | ||||||
| chr1:178909991
|
G | A | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1722+3124G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178909991 | ||||||
| chr1:178910020
|
G | T | 1 | a0001c0001t0033g0202 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1722+3153G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178910020 | ||||||
| chr1:178910035
|
A | G | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1722+3168A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178910035 | ||||||
| chr1:178910060
|
T | C | 36 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(33): Show | 36 | HG00544.hp1 HG00642.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.1722+3193T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178910060 | ||||||
| chr1:178910170
|
A | T | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1722+3303A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178910170 | ||||||
| chr1:178910210
|
G | A | 1 | a0001c0001t0028g0187 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1722+3343G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178910210 | ||||||
| chr1:178910406
|
A | T | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1722+3539A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178910406 | ||||||
| chr1:178910474
|
A | T | 1 | a0001c0001t0001g0250 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1722+3607A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178910474 | ||||||
| chr1:178910629
|
A | G | 2 | a0001c0001t0002g0078a0001c0001t0037g0077 | 2 | HG01243.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1722+3762A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178910629 | ||||||
| chr1:178910695
|
C | T | 7 | a0001c0001t0009g0138a0001c0001t0009g0140a0001c0001t0009g0141others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1722+3828C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178910695 | ||||||
| chr1:178910710
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1722+3843C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178910710 | ||||||
| chr1:178910842
|
G | A | 1 | a0001c0001t0006g0045 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1722+3975G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178910842 | ||||||
| chr1:178910855
|
C | T | 1 | a0001c0001t0002g0089 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1722+3988C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178910855 | ||||||
| chr1:178910951
|
G | T | 1 | a0001c0001t0006g0046 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1722+4084G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178910951 | ||||||
| chr1:178911048
|
A | G | 2 | a0001c0002t0005g0036a0001c0002t0005g0037 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1722+4181A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178911048 | ||||||
| chr1:178911135
|
C | T | 43 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(40): Show | 43 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1722+4268C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178911135 | ||||||
| chr1:178911314
|
T | C | 2 | a0001c0003t0017g0150a0001c0003t0017g0151 | 2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1722+4447T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178911314 | ||||||
| chr1:178911361
|
T | C | 2 | a0001c0001t0001g0265a0001c0001t0001g0277 | 2 | NA18983.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1722+4494T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178911361 | ||||||
| chr1:178911529
|
A | C | 4 | a0001c0001t0020g0004a0001c0001t0020g0038a0001c0003t0017g0150others(1): Show | 4 | HG01099.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1722+4662A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178911529 | ||||||
| chr1:178911558
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1722+4691G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178911558 | ||||||
| chr1:178911954
|
A | G | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1723-4376A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178911954 | ||||||
| chr1:178911955
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1723-4375T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178911955 | ||||||
| chr1:178912020
|
A | C | 22 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(19): Show | 22 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1723-4310A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178912020 | ||||||
| chr1:178912046
|
T | C | 22 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(19): Show | 22 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1723-4284T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178912046 | ||||||
| chr1:178912145
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1723-4185C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178912145 | ||||||
| chr1:178912170
|
T | C | 2 | a0001c0002t0003g0018a0001c0002t0003g0019 | 2 | NA19060.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1723-4160T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178912170 | ||||||
| chr1:178912364
|
C | T | 2 | a0001c0001t0001g0230a0001c0001t0001g0254 | 2 | NA19057.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1723-3966C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178912364 | ||||||
| chr1:178912604
|
T | A | 22 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(19): Show | 22 | HG01884.hp1 HG02055.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1723-3726T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178912604 | ||||||
| chr1:178912805
|
A | G | 2 | a0001c0002t0003g0018a0001c0002t0003g0019 | 2 | NA19060.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1723-3525A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178912805 | ||||||
| chr1:178912814
|
A | G | 2 | a0001c0001t0001g0215a0001c0001t0001g0285 | 2 | NA18967.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1723-3516A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178912814 | ||||||
| chr1:178913036
|
C | T | 1 | a0001c0001t0012g0152 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1723-3294C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178913036 | ||||||
| chr1:178913111
|
G | A | 8 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1723-3219G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178913111 | ||||||
| chr1:178913212
|
G | A | 1 | a0001c0001t0002g0116 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1723-3118G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178913212 | ||||||
| chr1:178913218
|
G | T | 1 | a0001c0001t0001g0197 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1723-3112G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178913218 | ||||||
| chr1:178913265
|
G | C | 9 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(6): Show | 9 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1723-3065G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178913265 | ||||||
| chr1:178913282
|
C | CA | 6 | a0001c0001t0001g0179a0001c0001t0001g0230a0001c0001t0001g0254others(3): Show | 6 | HG01099.hp1 NA18906.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.1723-3035dupA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 178913282 | |||||
| chr1:178913301
|
GA | G | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1723-3024delA | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr1 | 178913301 | |||||
| chr1:178913421
|
G | C | 1 | a0001c0001t0001g0159 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1723-2909G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178913421 | ||||||
| chr1:178913558
|
T | C | 1 | a0001c0001t0002g0079 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1723-2772T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178913558 | ||||||
| chr1:178913835
|
G | T | 7 | a0001c0002t0003g0015a0001c0002t0003g0016a0001c0002t0003g0027others(4): Show | 7 | HG00544.hp1 NA18962.hp2 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.1723-2495G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178913835 | ||||||
| chr1:178913908
|
G | A | 6 | a0001c0001t0012g0039a0001c0001t0012g0040a0001c0001t0012g0041others(3): Show | 6 | HG00738.hp2 HG02486.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.1723-2422G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178913908 | ||||||
| chr1:178914019
|
G | C | 1 | a0001c0001t0001g0251 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1723-2311G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178914019 | ||||||
| chr1:178914023
|
A | G | 2 | a0001c0001t0040g0148a0002c0005t0039g0042 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1723-2307A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178914023 | ||||||
| chr1:178914090
|
G | A | 25 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(22): Show | 25 | HG01099.hp1 HG01884.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.1723-2240G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178914090 | ||||||
| chr1:178914211
|
G | T | 1 | a0001c0001t0010g0074 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1723-2119G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178914211 | ||||||
| chr1:178914243
|
C | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1723-2087C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178914243 | ||||||
| chr1:178914375
|
G | T | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1723-1955G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178914375 | ||||||
| chr1:178914461
|
G | A | 28 | a0001c0001t0006g0043a0001c0001t0006g0044a0001c0001t0006g0045others(25): Show | 28 | HG01099.hp1 HG01884.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.1723-1869G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178914461 | ||||||
| chr1:178914645
|
G | T | 4 | a0001c0001t0002g0088a0001c0001t0002g0102a0001c0001t0002g0134others(1): Show | 4 | NA18941.hp2 NA18953.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.1723-1685G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178914645 | ||||||
| chr1:178914681
|
T | A | 1 | a0001c0001t0001g0171 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1723-1649T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178914681 | ||||||
| chr1:178914769
|
T | C | 13 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(10): Show | 13 | HG01346.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1723-1561T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178914769 | ||||||
| chr1:178914876
|
C | T | 3 | a0001c0001t0012g0152a0001c0001t0021g0075a0001c0001t0021g0076 | 3 | HG02895.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1723-1454C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178914876 | ||||||
| chr1:178915250
|
T | C | 3 | a0001c0001t0001g0195a0001c0001t0001g0220a0001c0001t0001g0227 | 3 | HG01106.hp2 HG01256.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1723-1080T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178915250 | ||||||
| chr1:178915629
|
T | A | 43 | a0001c0002t0003g0013a0001c0002t0003g0014a0001c0002t0003g0015others(40): Show | 43 | HG00099.hp1 HG00544.hp1 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1723-701T>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178915629 | ||||||
| chr1:178915632
|
G | T | 300 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(297): Show | 300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1723-698G>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178915632 | ||||||
| chr1:178915670
|
A | C | 1 | a0001c0001t0001g0186 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1723-660A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178915670 | ||||||
| chr1:178915720
|
T | C | 1 | a0001c0004t0004g0001 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1723-610T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178915720 | ||||||
| chr1:178915818
|
A | C | 2 | a0001c0001t0020g0004a0001c0001t0020g0038 | 2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1723-512A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178915818 |