Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MDLMN others(578): Show |
chr1 | 178720244 | 178926840 |
| a0002 | 0/0 | 583 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | MDLMN others(578): Show |
chr1 | 178720244 | 178926840 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1749 | 257 | 72 | 45 | 112 | 4 | 22 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ATGGA others(1744): Show |
chr1 | 178720244 | 178926840 | ||
| a0001c0002 | 0/0 | 1749 | 45 | 11 | 10 | 22 | 2 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ATGGA others(1744): Show |
chr1 | 178720244 | 178926840 | ||
| a0001c0003 | 0/0 | 1749 | 2 | 1 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ATGGA others(1744): Show |
chr1 | 178720244 | 178926840 | ||
| a0001c0004 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ATGGA others(1744): Show |
chr1 | 178720244 | 178926840 | ||
| a0002c0005 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ATGGA others(1744): Show |
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 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0002 | 0/0 | 7495 | 48 | 5 | 9 | 30 | 0 | 4 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0006 | 0/0 | 7495 | 8 | 8 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0007 | 0/0 | 7492 | 7 | 6 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7487): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0008 | 0/0 | 7492 | 7 | 7 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7487): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0009 | 0/0 | 7495 | 6 | 6 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0010 | 1/0 | 7492 | 6 | 1 | 1 | 3 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7487): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0011 | 0/0 | 7492 | 6 | 6 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7487): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0012 | 0/0 | 7495 | 4 | 1 | 1 | 0 | 0 | 2 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0013 | 0/0 | 7495 | 4 | 0 | 4 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0014 | 0/0 | 7495 | 3 | 0 | 0 | 3 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0015 | 0/0 | 7495 | 2 | 0 | 0 | 0 | 1 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0016 | 0/0 | 7495 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0018 | 0/0 | 7495 | 2 | 0 | 2 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0019 | 0/0 | 7495 | 2 | 2 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0020 | 0/0 | 7495 | 2 | 2 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0021 | 0/0 | 7495 | 2 | 2 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0025 | 0/1 | 7495 | 1 | 0 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0026 | 0/0 | 7495 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0027 | 0/0 | 7495 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0028 | 0/0 | 7495 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0029 | 0/0 | 7495 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0030 | 0/0 | 7495 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0031 | 0/0 | 7495 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0032 | 0/0 | 7495 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0033 | 0/0 | 7495 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0034 | 0/0 | 7495 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0035 | 0/0 | 7495 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0036 | 0/0 | 7495 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0037 | 0/0 | 7495 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0001t0039 | 0/0 | 7495 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0002t0003 | 0/0 | 7491 | 22 | 0 | 1 | 21 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7486): Show |
chr1 | 178720244 | 178926840 |
| a0001c0002t0004 | 0/0 | 7491 | 10 | 6 | 4 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7486): Show |
chr1 | 178720244 | 178926840 |
| a0001c0002t0005 | 0/0 | 7495 | 8 | 1 | 5 | 0 | 2 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0002t0016 | 0/0 | 7495 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0002t0022 | 0/0 | 7492 | 2 | 2 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7487): Show |
chr1 | 178720244 | 178926840 |
| a0001c0002t0023 | 0/0 | 7491 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7486): Show |
chr1 | 178720244 | 178926840 |
| a0001c0002t0024 | 0/0 | 7495 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0003t0017 | 0/0 | 7495 | 2 | 1 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| a0001c0004t0004 | 0/0 | 7491 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7486): Show |
chr1 | 178720244 | 178926840 |
| a0002c0005t0038 | 0/0 | 7495 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | ACTCT others(7490): Show |
chr1 | 178720244 | 178926840 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0156 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0180 | 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 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0208 | 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 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0241 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0268 | 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 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0293 | 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 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0007g0063 | 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 |
| a0001c0001t0007g0070 | 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 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0008g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0008g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0008g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0008g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0008g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0008g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0009g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0009g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0009g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0009g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0010g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0010g0060 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0010g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0010g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0010g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0010g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0011g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0011g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0011g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0011g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0011g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0011g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0012g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0012g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0013g0206 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0013g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0013g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0014g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0014g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0014g0274 | 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 |
| a0001c0001t0016g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0018g0079 | 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 |
| a0001c0001t0019g0145 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0020g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0020g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0021g0074 | 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 |
| a0001c0001t0025g0270 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0026g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0027g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0028g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0029g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0030g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0031g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0032g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0033g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0034g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0035g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0036g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0037g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0001t0039g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 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 | 1 | 0 | 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 | 0 | 1 | 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 |
| a0001c0002t0003g0030 | 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 |
| a0001c0002t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0004g0120 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0004g0124 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0002t0005g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0005g0035 | 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 |
| a0001c0002t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0016g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0022g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0022g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0023g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0002t0024g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0003t0017g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0003t0017g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0001c0004t0004g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| a0002c0005t0038g0041 | 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 | g0008 | EUR | GBR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | GBR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0153 | 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 | g0029 | 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 | g0297 | EAS | CHS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00544 | hp1 | a0001 | c0002 | t0003 | g0027 | EAS | CHS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00544 | hp2 | a0001 | c0001 | t0014 | g0274 | EAS | CHS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0288 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00642 | hp2 | a0001 | c0002 | t0003 | g0018 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00733 | hp1 | a0001 | c0002 | t0005 | g0012 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00738 | hp1 | a0001 | c0002 | t0005 | g0011 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00738 | hp2 | a0001 | c0001 | t0012 | g0040 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0301 | 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 | g0280 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01069 | hp2 | a0001 | c0002 | t0005 | g0035 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01070 | hp2 | a0001 | c0002 | t0004 | g0126 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01071 | hp1 | a0001 | c0002 | t0005 | g0036 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01071 | hp2 | a0001 | c0002 | t0004 | g0127 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01074 | hp2 | a0001 | c0002 | t0004 | g0119 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01099 | hp1 | a0001 | c0003 | t0017 | g0150 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01106 | hp1 | a0001 | c0001 | t0013 | g0207 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01168 | hp1 | a0001 | c0001 | t0018 | g0079 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0230 | 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 | g0303 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01192 | hp1 | a0001 | c0002 | t0004 | g0122 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01243 | hp1 | a0001 | c0001 | t0036 | g0076 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01255 | hp1 | a0001 | c0001 | t0013 | g0210 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01256 | hp2 | a0001 | c0001 | t0031 | g0179 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0235 | 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 | g0051 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01346 | hp2 | a0001 | c0001 | t0007 | g0072 | 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 | g0253 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01361 | hp1 | a0001 | c0001 | t0010 | g0254 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01496 | hp1 | a0001 | c0002 | t0005 | g0010 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | IBS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01516 | hp2 | a0001 | c0002 | t0005 | g0009 | EUR | IBS | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0045 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01952 | hp2 | a0001 | c0001 | t0013 | g0206 | 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 | g0220 | AMR | PEL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0198 | 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 | g0052 | 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 | g0004 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0143 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02129 | hp1 | a0001 | c0001 | t0034 | g0093 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0158 | 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 | g0132 | EAS | CDX | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CDX | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0065 | 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 | t0009 | g0111 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0141 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0049 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02280 | hp2 | a0002 | c0005 | t0038 | g0041 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02451 | hp1 | a0001 | c0001 | t0007 | g0064 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02451 | hp2 | a0001 | c0001 | t0027 | g0185 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0191 | 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 | g0167 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0121 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0117 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02622 | hp2 | a0001 | c0001 | t0020 | g0005 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02630 | hp1 | a0001 | c0001 | t0011 | g0062 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02698 | hp1 | a0001 | c0001 | t0012 | g0039 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02717 | hp2 | a0001 | c0001 | t0020 | g0037 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0046 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0003 | 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 | t0026 | g0171 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02809 | hp1 | a0001 | c0001 | t0009 | g0114 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02809 | hp2 | a0001 | c0001 | t0028 | g0155 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02818 | hp1 | a0001 | c0002 | t0004 | g0128 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02886 | hp1 | a0001 | c0001 | t0039 | g0147 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0043 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02895 | hp1 | a0001 | c0002 | t0004 | g0124 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02895 | hp2 | a0001 | c0001 | t0021 | g0074 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02896 | hp1 | a0001 | c0001 | t0011 | g0061 | 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 | g0075 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0063 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02922 | hp2 | a0001 | c0002 | t0022 | g0006 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02965 | hp1 | a0001 | c0001 | t0019 | g0145 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0137 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02970 | hp1 | a0001 | c0001 | t0035 | g0136 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02976 | hp2 | a0001 | c0001 | t0011 | g0067 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0125 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0073 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03098 | hp1 | a0001 | c0004 | t0004 | g0002 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0116 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03209 | hp1 | a0001 | c0002 | t0024 | g0148 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03225 | hp1 | a0001 | c0002 | t0005 | g0129 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03225 | hp2 | a0001 | c0001 | t0011 | g0068 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03453 | hp1 | a0001 | c0002 | t0023 | g0123 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0047 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0138 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0070 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0287 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03516 | hp2 | a0001 | c0002 | t0022 | g0007 | AFR | ESN | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0139 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0071 | AFR | GWD | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0058 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0048 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0281 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03669 | hp2 | a0001 | c0001 | t0012 | g0038 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | STU | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0305 | SAS | BEB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | STU | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18522 | hp1 | a0001 | c0002 | t0004 | g0120 | AFR | YRI | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | YRI | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18747 | hp1 | a0001 | c0001 | t0014 | g0265 | EAS | CHB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | YRI | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18906 | hp2 | a0001 | c0003 | t0017 | g0149 | AFR | YRI | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18939 | hp1 | a0001 | c0001 | t0033 | g0292 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0164 | 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 | g0173 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18943 | hp1 | a0001 | c0001 | t0032 | g0201 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0189 | 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 | g0266 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18952 | hp2 | a0001 | c0002 | t0003 | g0019 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0237 | 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 | g0057 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18959 | hp1 | a0001 | c0002 | t0003 | g0031 | 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 | t0030 | g0228 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18962 | hp2 | a0001 | c0002 | t0003 | g0034 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18969 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18971 | hp1 | a0001 | c0001 | t0029 | g0168 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18971 | hp2 | a0001 | c0001 | t0010 | g0240 | 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 | g0241 | 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 | g0056 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0294 | 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 | g0181 | 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 | g0263 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18989 | hp2 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18991 | hp1 | a0001 | c0001 | t0010 | g0239 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0203 | 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 | g0214 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18994 | hp1 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0279 | 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 | g0275 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18999 | hp1 | a0001 | c0002 | t0003 | g0017 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19000 | hp2 | a0001 | c0002 | t0003 | g0026 | 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 | g0238 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19002 | hp2 | a0001 | c0002 | t0003 | g0014 | 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 | g0033 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0209 | 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 | g0099 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19030 | hp1 | a0001 | c0001 | t0012 | g0151 | AFR | LWK | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0042 | AFR | LWK | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19043 | hp2 | a0001 | c0001 | t0016 | g0183 | 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 | g0267 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19057 | hp2 | a0001 | c0002 | t0003 | g0015 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19060 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0260 | 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 | g0152 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19065 | hp2 | a0001 | c0001 | t0010 | g0257 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19070 | hp2 | a0001 | c0001 | t0037 | g0291 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0174 | 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 | g0157 | 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 | g0212 | 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 | g0268 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19087 | hp2 | a0001 | c0002 | t0003 | g0028 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19091 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19240 | hp1 | a0001 | c0001 | t0009 | g0118 | AFR | YRI | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | YRI | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ASW | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA20129 | hp2 | a0001 | c0001 | t0011 | g0069 | AFR | ASW | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | GIH | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | GIH | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | CLM | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0013 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0140 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02486 | hp2 | a0001 | c0001 | t0019 | g0146 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0112 | AFR | ACB | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0066 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | USA | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | USA | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0236 | 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 | t0008 | g0142 | AFR | LWK | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0025 | g0270 | REF | REF | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0010 | g0060 | REF | REF | RALGPS2_chr1_178720244_178926840 | RALGPS2 | chr1 | 178720244 | 178926840 |
| view | 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 |
| view | 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 | a0001c0002 a0001c0004 |
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 |
| view | 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 | a0001c0001t0008 | 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 | a0001c0001t0010 | 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 | 35 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(32): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): 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 | 2 | a0001c0001t0008 a0001c0001t0021 |
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 | a0001c0001t0039 a0002c0005t0038 |
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 | a0001c0001t0039 a0002c0005t0038 |
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 | a0001c0001t0039 a0002c0005t0038 |
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 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0005 others(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 | 27 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(24): 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 | a0001c0002t0005 a0001c0002t0024 |
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 | a0001c0001t0037 | 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 | 3 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0009 |
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 | 3 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0009 |
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 | a0001c0001t0032 | 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 | a0001c0002t0023 | 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 | 2 | a0001c0001t0008 a0001c0001t0009 |
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 | ||||||
| chr1:178919233 | 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 | a0001c0001t0026 | 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 | a0001c0001t0036 | 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 | 29 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0007 others(26): 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 | a0001c0001t0007 a0001c0001t0011 |
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 | a0001c0001t0031 | 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 | a0001c0001t0027 | 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 | a0001c0001t0035 | 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 | a0001c0001t0032 | 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 | a0001c0001t0028 | 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 | a0001c0001t0039 | 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 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0023 others(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 | a0001c0001t0033 | 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 | a0001c0002t0024 | 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 | a0001c0001t0034 | 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 | a0001c0001t0030 | 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 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0018 others(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 | a0001c0001t0029 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5328G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 20/20 | 5328 | chr1 | 178921687 |
| view | 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 | a0001c0004t0004g0002 | 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 | a0001c0001t0002g0305 | 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 | 153 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0156 others(150): Show |
153 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(150): 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 | a0001c0001t0012g0151 | 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 | 153 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0156 others(150): Show |
153 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(150): 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 | a0001c0001t0019g0145 a0001c0001t0019g0146 a0001c0001t0039g0147 others(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 | a0001c0001t0002g0152 | 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 | a0001c0001t0001g0304 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0020g0005 |
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 | 39 | a0001c0001t0001g0154 a0001c0001t0019g0145 a0001c0001t0019g0146 others(36): 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0303 | 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 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0302 a0001c0001t0008g0137 a0001c0001t0008g0138 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0028g0155 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(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 | 167 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(164): Show |
167 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(164): 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | 272 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): 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 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0131 a0001c0001t0002g0132 |
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 | a0001c0001t0002g0130 | 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 | 45 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(42): 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | 152 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(149): Show |
152 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.-84+3542A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178728961 | |||||||
| chr1:178729016 | A | G | 301 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(298): Show |
302 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.-84+3597A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178729016 | |||||||
| chr1:178729201 | T | G | 227 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(224): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): 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 | a0001c0001t0001g0281 | 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 | a0001c0001t0002g0077 a0001c0001t0036g0076 |
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 | a0001c0001t0035g0136 | 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 | a0001c0001t0001g0156 a0001c0002t0004g0119 a0001c0002t0004g0120 others(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 | a0001c0001t0001g0302 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0059 a0001c0001t0020g0005 a0001c0001t0020g0037 others(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 | a0001c0001t0001g0280 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0035g0136 | 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 | a0001c0002t0005g0035 a0001c0002t0005g0036 |
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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0157 a0001c0001t0001g0296 a0001c0001t0002g0078 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 |
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 | 43 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(40): 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 | a0001c0001t0001g0158 | 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 | a0001c0002t0004g0013 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0158 a0001c0001t0002g0305 a0001c0001t0019g0145 others(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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 others(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 | a0001c0002t0004g0013 | 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 | a0001c0001t0028g0155 | 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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0002t0004g0013 | 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 | a0001c0001t0001g0158 a0001c0001t0001g0215 a0001c0001t0001g0216 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0059 others(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 | 35 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(32): Show |
35 | HG00438.hp2 HG00597.hp2 HG01069.hp1 others(32): 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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0275 others(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 | a0001c0001t0019g0146 | 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 | a0001c0001t0001g0154 a0001c0001t0001g0157 a0001c0001t0001g0161 others(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 | 35 | a0001c0001t0001g0160 a0001c0001t0006g0043 a0001c0001t0006g0044 others(32): 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 | a0001c0001t0002g0078 a0001c0001t0002g0099 a0001c0001t0002g0100 others(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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0002g0286 | 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 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0047 others(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 | a0001c0001t0001g0050 | 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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0047 others(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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0271 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-84+6119C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178731538 | |||||||
| chr1:178731700 | A | G | 15 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
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 | a0001c0001t0001g0214 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0016g0183 | 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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0002g0099 a0001c0001t0039g0147 a0001c0002t0005g0129 others(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 |
39 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(36): 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 | a0001c0002t0004g0128 a0001c0002t0005g0008 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | ||||||
| chr1:178732523 | T | C | 2 | a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0009g0118 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0222 a0001c0001t0007g0063 a0001c0001t0007g0064 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0002g0115 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0144 |
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 | a0001c0002t0003g0026 a0001c0002t0003g0032 a0001c0002t0003g0033 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | 61 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(58): Show |
61 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(58): 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 | a0001c0002t0004g0126 a0001c0002t0004g0127 |
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 | 151 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(148): 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 | a0001c0001t0036g0076 | 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 | a0001c0001t0035g0136 | 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | 34 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(31): 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 | a0002c0005t0038g0041 | 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 | a0001c0001t0028g0155 | 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 | a0001c0002t0024g0148 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-84+8947A>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178734366 | |||||||
| chr1:178734777 | A | G | 6 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | 88 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(85): Show |
88 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(85): 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 | a0001c0001t0002g0133 a0001c0001t0012g0038 a0001c0001t0012g0039 others(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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0001g0296 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | 128 | a0001c0001t0001g0131 a0001c0001t0001g0243 a0001c0001t0002g0003 others(125): 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 | a0001c0001t0001g0241 a0001c0001t0001g0269 a0001c0001t0001g0275 others(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 | a0001c0001t0002g0083 a0001c0001t0002g0100 a0001c0001t0021g0074 others(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 | a0001c0001t0001g0163 a0001c0001t0001g0184 a0001c0001t0001g0195 others(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 | a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0002t0003g0014 | 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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | 44 | a0001c0001t0001g0243 a0001c0002t0003g0001 a0001c0002t0003g0014 others(41): 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0164 a0001c0001t0012g0151 others(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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0002g0110 a0001c0001t0002g0113 a0001c0001t0002g0290 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0153 others(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 | 35 | a0001c0001t0001g0243 a0001c0002t0003g0001 a0001c0002t0003g0014 others(32): 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 | 288 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(285): Show |
289 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(286): 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 | a0001c0001t0001g0191 | 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 | a0001c0001t0001g0297 | 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0114 others(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 | a0001c0001t0006g0044 | 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 | 23 | a0001c0001t0001g0243 a0001c0002t0003g0001 a0001c0002t0003g0014 others(20): 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 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0047 others(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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0019g0145 a0001c0001t0019g0146 a0001c0002t0005g0008 |
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 | a0001c0002t0024g0148 | 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 | a0001c0001t0010g0257 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0001g0154 a0001c0001t0001g0157 a0001c0001t0001g0159 others(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 | a0001c0002t0004g0126 a0001c0002t0004g0127 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0002t0005g0129 | 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 | a0001c0001t0001g0154 a0001c0001t0001g0157 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0180 others(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 | a0001c0001t0001g0161 a0001c0001t0006g0042 a0001c0001t0006g0043 others(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 | a0001c0001t0001g0162 a0001c0001t0002g0077 a0001c0001t0002g0290 others(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 | a0001c0001t0008g0140 a0001c0001t0008g0141 a0001c0001t0008g0142 |
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 | a0001c0001t0001g0158 a0001c0001t0001g0215 |
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 | a0001c0001t0009g0114 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0039g0147 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0222 a0001c0001t0001g0237 a0001c0001t0001g0238 |
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 | a0001c0001t0012g0038 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0028g0155 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0144 |
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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0014g0274 | 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 | a0001c0001t0001g0160 | 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 | 24 | a0001c0001t0001g0054 a0001c0001t0001g0243 a0001c0002t0003g0001 others(21): 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0302 | 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 | a0001c0001t0001g0236 a0001c0001t0001g0256 |
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 | a0001c0001t0001g0242 a0001c0001t0001g0268 |
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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0001g0269 a0001c0001t0001g0275 a0001c0002t0005g0129 |
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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0001g0214 a0001c0001t0001g0284 |
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 | a0001c0001t0001g0165 a0001c0001t0001g0192 |
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 | a0001c0001t0001g0056 a0001c0001t0001g0154 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0166 a0001c0001t0001g0193 a0001c0001t0001g0219 others(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 | 8 | a0001c0001t0019g0145 a0001c0002t0005g0008 a0001c0002t0005g0009 others(5): Show |
8 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(5): 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0001g0248 a0001c0001t0012g0151 a0001c0001t0021g0074 others(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 | a0001c0001t0001g0059 a0001c0001t0001g0144 a0001c0001t0009g0111 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0189 |
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 | a0001c0001t0001g0203 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0002g0078 | 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 | a0001c0001t0001g0303 | 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 | a0001c0001t0002g0082 a0001c0001t0002g0130 |
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 | a0001c0001t0001g0154 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 others(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 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0114 others(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 | a0001c0001t0001g0161 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0007g0072 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | |||||||
| chr1:178744699 | C | T | 63 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0009g0114 | 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 | a0001c0001t0001g0190 a0001c0001t0001g0223 a0001c0001t0001g0249 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0019g0146 others(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 | 64 | a0001c0001t0001g0054 a0001c0001t0001g0175 a0001c0001t0001g0285 others(61): 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0002t0004g0013 a0001c0002t0004g0119 a0001c0002t0004g0120 others(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 | a0001c0001t0009g0117 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0001g0226 a0001c0001t0001g0234 a0001c0001t0001g0235 others(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 | a0001c0001t0001g0284 | 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 | a0001c0002t0003g0023 a0001c0002t0003g0025 |
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 | a0001c0001t0001g0174 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0010g0254 | 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 | a0001c0001t0006g0043 | 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 | a0001c0001t0001g0059 a0001c0001t0001g0187 a0001c0001t0001g0188 others(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 | 111 | a0001c0001t0001g0054 a0001c0001t0001g0131 a0001c0001t0001g0216 others(108): 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 | a0001c0001t0002g0084 a0001c0001t0002g0295 a0001c0001t0020g0005 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0001g0256 | 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 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0028g0155 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0002t0005g0129 | 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 | a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0006g0045 | 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 | a0001c0001t0018g0079 a0001c0001t0018g0096 |
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 | a0001c0001t0028g0155 | 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 | 72 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(69): 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 | a0001c0001t0001g0189 | 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 | 34 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(31): 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 | a0001c0002t0004g0013 a0001c0002t0004g0128 |
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 | a0001c0001t0001g0226 a0001c0001t0001g0234 a0001c0001t0001g0235 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0156 a0001c0001t0001g0241 others(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 | a0001c0002t0004g0013 | 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 | a0001c0001t0011g0067 a0001c0001t0011g0068 a0001c0001t0011g0069 |
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 | a0001c0001t0039g0147 | 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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0283 |
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 | a0001c0002t0005g0129 | 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 | a0001c0002t0005g0129 | 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 | a0001c0002t0005g0129 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0191 a0001c0001t0001g0208 a0001c0001t0001g0209 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0002t0005g0035 a0001c0002t0005g0036 |
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 | a0001c0001t0001g0234 a0001c0001t0001g0243 a0001c0001t0006g0042 others(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 | a0001c0001t0001g0052 a0001c0001t0001g0261 a0001c0001t0001g0267 others(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 | a0001c0001t0001g0224 | 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 | a0001c0002t0005g0012 | 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0001g0231 a0001c0001t0001g0303 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(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 | 45 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(42): 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 | a0001c0001t0006g0044 | 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0047 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0035g0136 | 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 | a0001c0002t0004g0126 a0001c0002t0004g0127 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | 36 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(33): 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0010g0058 | 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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0001g0301 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0028g0155 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0006g0044 | 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 | a0001c0001t0001g0215 a0001c0001t0002g0078 a0001c0001t0006g0042 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0173 | 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 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0296 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0192 a0001c0002t0004g0128 |
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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0001g0158 a0001c0001t0001g0215 |
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 | 42 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(39): 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 | a0001c0002t0003g0018 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0002g0081 a0001c0001t0002g0094 a0001c0001t0002g0095 others(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 | a0001c0001t0001g0173 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-83-23324G>A | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178753358 | |||||||
| chr1:178753366 | A | T | 1 | a0001c0001t0019g0146 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0012g0039 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0284 | 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 | a0001c0001t0039g0147 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0028g0155 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0214 a0001c0001t0001g0284 |
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 | a0001c0001t0009g0117 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | 43 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(40): 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | 136 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(133): 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 | a0001c0001t0010g0058 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0026g0171 | 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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0002g0290 a0001c0001t0002g0293 a0001c0001t0002g0294 others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-83-20022A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178756660 | |||||||
| chr1:178756754 | G | A | 8 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | 34 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(31): 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 | a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0018g0079 a0001c0001t0018g0096 |
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 | a0001c0001t0001g0202 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0002g0081 a0001c0001t0002g0094 a0001c0001t0002g0095 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0002t0024g0148 | 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | 151 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(148): 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 | a0001c0001t0001g0131 a0001c0001t0002g0132 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0007g0071 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0001g0131 a0001c0001t0002g0132 a0001c0001t0034g0093 |
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 | a0001c0001t0001g0055 a0001c0001t0001g0215 a0001c0001t0001g0282 others(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 | 83 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(80): 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0144 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0019g0145 a0001c0001t0019g0146 a0001c0001t0035g0136 |
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 | a0001c0001t0001g0301 | 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 | a0001c0001t0001g0276 | 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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0001g0200 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(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 | a0001c0001t0001g0187 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0001g0219 a0001c0001t0001g0256 a0001c0001t0008g0137 others(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 | a0001c0001t0001g0173 a0001c0001t0001g0237 a0001c0001t0001g0303 others(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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0008g0140 | 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 | a0001c0001t0006g0042 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0001g0189 | 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0006g0044 a0001c0001t0006g0045 a0001c0001t0006g0046 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0259 |
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 | a0001c0001t0019g0145 a0001c0001t0019g0146 |
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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0160 a0001c0001t0001g0166 |
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 | 151 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(148): 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 | 34 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(31): 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0002t0003g0030 | 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 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0114 others(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 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0104 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0002t0004g0128 | 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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0001g0164 a0001c0001t0001g0189 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0013g0206 a0001c0001t0013g0207 a0001c0001t0013g0210 others(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 | a0001c0001t0039g0147 | 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 | a0001c0002t0024g0148 | 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 | 34 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(31): 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 | a0001c0001t0001g0258 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0001g0242 a0001c0001t0001g0258 a0001c0001t0001g0268 |
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 | a0001c0001t0006g0046 | 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 | 201 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(198): 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0028g0155 | 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 | a0001c0002t0003g0018 | 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 | a0001c0001t0036g0076 | 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 | a0001c0001t0009g0112 a0001c0001t0009g0114 |
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 | a0001c0001t0001g0238 a0001c0001t0001g0268 a0001c0001t0001g0280 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0236 a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0016g0183 | 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 | a0001c0001t0030g0228 | 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 | a0001c0002t0005g0009 | 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0204 | 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 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
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 | a0001c0001t0033g0292 | 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 | a0001c0001t0036g0076 | 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 | a0001c0001t0001g0303 | 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 | a0001c0001t0001g0190 | 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 | a0001c0002t0004g0119 a0001c0002t0004g0120 a0001c0002t0004g0121 others(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 | a0001c0001t0001g0284 a0001c0001t0012g0038 a0001c0001t0012g0039 others(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 | 128 | a0001c0001t0001g0131 a0001c0001t0001g0214 a0001c0001t0002g0003 others(125): 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 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0001g0182 | 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0001g0260 | 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0002g0135 | 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 | a0001c0001t0014g0265 a0001c0001t0014g0266 |
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 | 47 | a0001c0001t0001g0051 a0001c0001t0001g0158 a0001c0001t0001g0174 others(44): 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 | a0001c0001t0002g0294 a0001c0001t0007g0070 a0001c0001t0012g0038 others(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 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0159 others(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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | 34 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(31): 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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0008g0141 | 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 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0114 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0009g0118 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | 14 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0144 others(11): Show |
14 | HG00558.hp1 HG01243.hp2 HG01257.hp2 others(11): 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0190 | 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 | a0001c0001t0002g0132 | 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 | a0001c0001t0002g0089 a0001c0001t0002g0099 a0001c0001t0002g0135 |
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 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0262 others(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 | |||||||
| chr1:178769621 | G | T | 1 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0273 | 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 | 36 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(33): 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | 122 | a0001c0001t0001g0212 a0001c0001t0001g0280 a0001c0001t0002g0003 others(119): 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 | a0001c0001t0002g0134 a0001c0001t0006g0042 a0001c0001t0006g0043 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0221 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0001g0227 a0001c0001t0001g0251 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
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 | a0001c0001t0001g0172 a0001c0001t0001g0217 a0001c0001t0001g0262 others(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 | a0001c0001t0034g0093 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | a0001c0002t0004g0119 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0016g0183 | 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 | a0001c0001t0001g0192 a0001c0001t0001g0222 a0001c0001t0001g0269 others(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 | 22 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(19): 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0047 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0221 |
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 | a0001c0001t0008g0137 a0001c0001t0008g0138 |
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 | 202 | a0001c0001t0001g0055 a0001c0001t0001g0131 a0001c0001t0001g0154 others(199): 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0001g0221 a0001c0001t0006g0042 a0001c0001t0006g0043 others(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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0001g0236 a0001c0001t0001g0256 |
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 | a0001c0001t0001g0230 | 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 | 56 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(53): 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 others(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 | a0001c0001t0001g0282 | 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 | a0001c0001t0006g0042 | 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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | 287 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(284): Show |
288 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.-83-3375A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178773307 | |||||||
| chr1:178773401 | A | G | 45 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(42): 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 |
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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
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 | a0001c0001t0002g0115 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-83-2976G>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 1/19 | chr1 | 178773706 | |||||||
| chr1:178773774 | C | T | 1 | a0001c0001t0001g0159 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0156 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0104 others(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 | a0001c0001t0001g0204 | 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 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0001g0211 a0001c0001t0001g0221 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0015g0108 a0001c0001t0015g0109 |
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 | a0001c0001t0001g0158 a0001c0001t0001g0215 |
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 | a0001c0001t0001g0164 | 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 | a0001c0001t0001g0304 | 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 | a0001c0001t0035g0136 | 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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0002t0004g0125 a0001c0002t0023g0123 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0261 a0001c0001t0001g0284 a0001c0001t0006g0047 others(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 | a0001c0001t0001g0161 a0001c0001t0001g0172 a0001c0001t0001g0180 others(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 | 72 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(69): Show |
72 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(69): 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 | a0001c0001t0019g0145 a0001c0001t0019g0146 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0001g0170 | 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 | 45 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(42): 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 | a0001c0001t0002g0077 | 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 | a0001c0001t0014g0265 a0001c0001t0014g0266 a0001c0001t0014g0274 |
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 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(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 | 34 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(31): 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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | a0001c0002t0003g0016 a0001c0002t0003g0017 a0001c0002t0003g0026 others(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 | 36 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(33): 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 | a0001c0001t0001g0272 | 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 | a0001c0001t0035g0136 | 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 | a0001c0001t0010g0239 | 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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0173 a0001c0001t0001g0211 a0001c0001t0001g0221 |
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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0159 a0001c0001t0001g0205 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(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 | a0001c0001t0001g0176 | 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 | a0001c0002t0004g0013 | 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 | a0001c0001t0010g0058 a0001c0002t0004g0013 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0010g0254 | 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | 81 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(78): 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 | a0001c0002t0003g0016 a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | a0001c0001t0039g0147 | 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 | a0001c0002t0023g0123 | 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 | a0001c0001t0018g0079 a0001c0001t0018g0096 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.57+1482T>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 2/19 | chr1 | 178778303 | |||||||
| chr1:178778336 | A | G | 1 | a0001c0002t0005g0129 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0004t0004g0002 | 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 | a0001c0001t0001g0261 a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0261 | 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 | a0001c0001t0001g0261 | 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 | a0001c0001t0002g0084 a0001c0001t0002g0087 a0001c0001t0002g0103 |
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 | a0001c0001t0032g0201 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0010g0239 | 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 | 1 | a0001c0002t0003g0001 | 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 | a0001c0001t0001g0236 | 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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0016g0183 | 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 | a0001c0002t0004g0013 a0001c0002t0004g0128 |
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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0001g0052 | 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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0039g0147 | 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 | a0001c0001t0035g0136 | 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 | a0001c0001t0002g0289 | 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 | a0001c0001t0001g0226 a0001c0001t0001g0234 a0001c0001t0001g0235 others(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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0230 | 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 | 45 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(42): 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 | a0001c0002t0004g0013 | 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 | a0001c0001t0019g0145 | 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 | a0001c0002t0023g0123 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0001g0202 | 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | 150 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(147): 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 | 69 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0056 others(66): Show |
69 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(66): 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 | a0001c0001t0001g0249 | 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 | a0001c0001t0034g0093 | 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 | a0001c0001t0001g0153 a0001c0001t0006g0042 a0001c0001t0006g0043 others(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 | 34 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(31): 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 | a0001c0001t0001g0169 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0001t0002g0305 | 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 | 43 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(40): 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 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | 150 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(147): 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 | 150 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(147): 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 | 45 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(42): 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 | a0001c0001t0001g0170 | 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 | a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0002t0005g0035 a0001c0002t0005g0036 |
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 | a0001c0001t0001g0161 a0001c0001t0001g0172 a0001c0001t0001g0180 others(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 | a0001c0001t0006g0043 | 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 | a0001c0001t0019g0145 a0001c0001t0019g0146 |
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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0001g0161 a0001c0001t0001g0180 a0001c0001t0001g0181 others(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 | a0001c0001t0006g0043 | 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 | a0001c0002t0004g0013 | 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 | a0001c0002t0004g0013 | 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 | a0001c0001t0002g0289 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0002g0289 | 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 | a0001c0001t0002g0289 | 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 | a0001c0001t0009g0117 | 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 | a0001c0001t0002g0289 | 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 | a0001c0001t0002g0289 | 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 | a0001c0001t0002g0289 a0001c0002t0005g0008 |
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 | a0001c0001t0002g0289 | 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 | a0001c0001t0002g0289 | 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 | a0001c0001t0002g0289 | 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 | a0001c0001t0002g0289 | 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 | a0001c0001t0006g0044 | 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 | a0001c0002t0004g0119 | 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 | a0001c0001t0002g0132 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0011g0073 | 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 | a0001c0001t0007g0065 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0028g0155 | 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 | a0001c0001t0030g0228 | 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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0001g0165 | 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 | a0001c0001t0002g0132 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | 150 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(147): 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 | a0001c0001t0011g0073 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0006g0044 | 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 | a0001c0001t0001g0248 | 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 | a0001c0001t0001g0214 | 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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | 45 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(42): 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0195 | 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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | a0001c0001t0001g0157 a0001c0001t0006g0046 a0001c0001t0035g0136 |
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 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0159 others(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 | a0001c0001t0006g0046 a0001c0001t0035g0136 |
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 | a0001c0003t0017g0150 | 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 | a0001c0001t0002g0130 | 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 | a0001c0001t0002g0082 | 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 | a0001c0001t0001g0054 a0001c0001t0001g0184 a0001c0001t0001g0226 others(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 | a0001c0001t0001g0172 a0001c0001t0001g0193 a0001c0001t0001g0219 others(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 | a0001c0001t0006g0047 a0001c0001t0006g0048 |
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 | a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0001g0255 a0001c0001t0006g0042 a0001c0001t0006g0043 |
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 | a0001c0001t0006g0045 | 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 | a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | a0001c0001t0001g0224 a0001c0001t0001g0244 a0001c0001t0001g0245 others(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 | 113 | a0001c0001t0001g0131 a0001c0001t0001g0218 a0001c0001t0001g0223 others(110): 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0181 a0001c0001t0006g0046 |
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 | a0001c0001t0035g0136 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | 43 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(40): 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 | a0001c0001t0011g0061 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 others(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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0026g0171 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | a0001c0002t0005g0129 | 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 | a0001c0001t0001g0055 | 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 | 45 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(42): 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | 10 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0144 others(7): Show |
10 | HG00558.hp1 HG01243.hp2 HG01257.hp2 others(7): 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0009g0117 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0211 a0001c0001t0001g0221 |
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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | 99 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0156 others(96): 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 | a0001c0001t0002g0132 | 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 | a0001c0002t0004g0120 | 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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0002g0152 | 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 | a0001c0001t0002g0078 | 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 | a0001c0002t0016g0029 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0002g0081 a0001c0001t0002g0094 a0001c0001t0002g0286 |
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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0001g0174 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0272 |
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 | 43 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(40): 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | 43 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(40): 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0039g0147 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0001g0153 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0001g0164 a0001c0001t0001g0189 |
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 | a0001c0001t0001g0231 a0001c0001t0001g0252 a0001c0001t0001g0303 |
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 | a0001c0001t0001g0215 a0001c0001t0001g0264 a0001c0001t0001g0267 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0157 a0001c0001t0001g0162 others(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 | a0001c0001t0001g0255 | 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 | a0001c0001t0001g0236 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | 285 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0055 others(282): Show |
286 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(283): 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 | a0002c0005t0038g0041 | 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 | a0001c0001t0019g0145 a0001c0001t0019g0146 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0002t0004g0128 | 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 | a0001c0001t0001g0226 a0001c0001t0001g0234 a0001c0001t0001g0235 others(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 | a0001c0002t0005g0129 | 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 | 75 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(72): 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 | a0001c0001t0006g0042 | 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0177 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0033g0292 | 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 | a0001c0001t0039g0147 | 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 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
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 | a0001c0001t0006g0046 | 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 | a0001c0001t0009g0116 | 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 | a0001c0002t0005g0035 a0001c0002t0005g0036 |
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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 |
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 | a0001c0001t0039g0147 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0229 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0002c0005t0038g0041 | 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0131 a0001c0001t0001g0144 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0077 a0001c0001t0002g0092 others(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 | a0001c0001t0007g0065 a0001c0001t0008g0143 a0001c0001t0011g0073 others(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 | 26 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(23): 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 | a0001c0001t0020g0037 a0001c0002t0003g0021 a0001c0002t0003g0024 others(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 | a0001c0001t0001g0251 a0001c0001t0012g0151 a0001c0002t0005g0008 others(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 | a0001c0001t0006g0044 | 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0006g0045 | 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 | a0001c0001t0001g0256 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0011g0067 a0001c0001t0011g0068 a0001c0001t0011g0069 |
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 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
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 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(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 | a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0019g0145 a0001c0001t0019g0146 |
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 | a0001c0001t0001g0190 | 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 | a0001c0001t0020g0037 | 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 | a0001c0001t0020g0005 | 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0002g0081 a0001c0001t0002g0094 a0001c0001t0002g0286 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | 43 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(40): 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0006g0044 a0001c0001t0009g0111 a0001c0001t0009g0112 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0039g0147 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | a0001c0001t0001g0153 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0104 others(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 | a0001c0001t0002g0152 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0230 | 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 | a0001c0001t0001g0160 a0001c0001t0001g0166 |
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 | a0001c0001t0008g0138 | 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 | a0001c0001t0001g0131 a0001c0001t0001g0192 a0001c0001t0002g0084 others(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 | a0001c0001t0002g0080 | 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 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0153 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0006g0044 | 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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(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 | a0001c0001t0002g0095 a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | 202 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(199): 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
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 | a0001c0001t0001g0203 a0001c0001t0010g0240 a0001c0001t0010g0257 |
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 | a0001c0001t0001g0296 | 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 | a0001c0001t0001g0247 | 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 | a0001c0001t0001g0252 | 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 | a0001c0001t0006g0047 a0001c0001t0006g0048 a0001c0001t0006g0049 |
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 | a0001c0002t0004g0013 | 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 | a0001c0001t0011g0061 a0001c0001t0011g0062 |
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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0002g0133 | 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 | a0001c0001t0001g0174 | 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 | a0001c0001t0035g0136 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0001t0028g0155 | 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 | a0001c0001t0009g0111 | 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 | a0001c0002t0004g0013 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0191 a0001c0001t0001g0209 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0237 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | 12 | a0001c0001t0001g0244 a0001c0001t0001g0247 a0001c0001t0001g0272 others(9): Show |
12 | HG01884.hp2 HG02155.hp1 HG02559.hp1 others(9): 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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | 83 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0054 others(80): 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0196 | 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 | a0001c0001t0002g0130 | 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 | a0001c0001t0002g0078 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0001g0177 a0001c0001t0006g0042 a0001c0001t0006g0043 others(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 | a0001c0001t0039g0147 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | 22 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(19): 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0002t0005g0035 a0001c0002t0005g0036 |
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 | a0001c0001t0006g0047 a0001c0001t0006g0048 a0001c0001t0006g0049 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
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 | a0001c0001t0011g0067 | 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 | a0001c0001t0035g0136 | 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 | a0001c0002t0004g0013 | 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 | a0001c0001t0008g0140 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | 150 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(147): 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 | a0001c0001t0001g0166 a0001c0001t0006g0042 a0001c0001t0006g0043 others(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 | a0001c0001t0010g0239 | 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 | a0001c0001t0008g0141 | 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | 36 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(33): 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 | 34 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(31): 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 | a0001c0001t0001g0182 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0002g0290 a0001c0001t0002g0293 a0001c0001t0002g0294 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
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 | a0001c0001t0019g0145 a0001c0001t0019g0146 |
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 | a0001c0002t0005g0035 a0001c0002t0005g0036 |
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 | a0001c0002t0003g0015 a0001c0002t0003g0019 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0184 | 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 | a0001c0001t0002g0288 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0303 |
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 | a0001c0001t0002g0077 | 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 | a0001c0001t0001g0197 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.214-209A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | chr1 | 178807836 | |||||||
| chr1:178808255 | T | C | 1 | a0001c0001t0001g0176 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0001t0036g0076 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 others(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 | 45 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(42): 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 | a0001c0001t0002g0084 a0001c0001t0002g0087 a0001c0001t0002g0103 |
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 | a0001c0001t0001g0194 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0002t0004g0013 a0001c0002t0004g0119 a0001c0002t0004g0120 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0056 others(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 | a0001c0001t0001g0187 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | 16 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0016 others(13): 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 | a0001c0001t0001g0280 | 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 | 36 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(33): 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 | a0001c0001t0001g0200 a0001c0001t0001g0268 a0001c0001t0006g0042 others(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 | a0001c0001t0001g0298 a0001c0001t0002g0294 a0001c0001t0007g0063 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0001t0001g0236 a0001c0001t0001g0256 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0001t0035g0136 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 others(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 | a0001c0001t0019g0145 a0001c0001t0019g0146 |
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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0006g0047 a0001c0001t0006g0048 a0001c0001t0006g0049 |
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 | 201 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(198): 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 | a0001c0001t0007g0071 | 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 | a0001c0001t0002g0077 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0006g0042 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0177 | 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 | 34 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(31): 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 | a0001c0002t0024g0148 | 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 | a0001c0001t0035g0136 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0002g0286 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0006g0044 | 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 | a0001c0001t0001g0203 a0001c0001t0001g0209 a0001c0001t0001g0262 others(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 | a0001c0001t0008g0143 a0001c0001t0009g0111 a0001c0001t0009g0112 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0154 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0002g0081 a0001c0001t0002g0094 a0001c0001t0002g0286 |
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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0144 |
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 | a0001c0002t0005g0035 a0001c0002t0005g0036 |
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 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0001g0054 a0001c0001t0001g0131 a0001c0001t0001g0187 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0019g0145 a0001c0001t0019g0146 a0001c0001t0035g0136 |
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 | a0001c0001t0001g0227 a0001c0001t0001g0251 a0001c0001t0030g0228 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
2 | HG01099.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.387+3334C>T | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 6/19 | chr1 | 178814738 | |||||||
| chr1:178814854 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0189 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0039g0147 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0010g0254 | 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 | 151 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(148): 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 | a0001c0001t0001g0284 | 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 | a0001c0001t0002g0132 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0002c0005t0038g0041 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0001g0160 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | 151 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(148): 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | 232 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(229): 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0015g0108 a0001c0001t0015g0109 |
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 | a0001c0001t0001g0241 a0001c0001t0001g0262 a0001c0001t0001g0279 others(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 | 267 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(264): Show |
268 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(265): 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 | a0001c0001t0001g0209 a0001c0001t0002g0077 a0001c0001t0006g0047 others(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 | a0001c0001t0006g0042 | 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 | a0001c0001t0001g0302 | 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 | 34 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(31): 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 | a0001c0001t0014g0266 | 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 | a0001c0002t0022g0006 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | a0001c0001t0001g0161 | 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 | a0002c0005t0038g0041 | 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 | a0001c0002t0024g0148 | 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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0001g0059 a0001c0001t0001g0144 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0001g0215 a0001c0001t0001g0262 a0001c0001t0001g0267 others(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 | a0001c0001t0001g0192 a0001c0001t0001g0260 a0001c0001t0002g0003 others(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 | 45 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(42): 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 | a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | a0001c0001t0030g0228 | 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 | a0001c0001t0001g0211 a0001c0001t0001g0221 |
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 | a0001c0001t0001g0190 | 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 | 150 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(147): 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0011g0062 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0009g0112 a0001c0001t0009g0114 |
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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0001t0018g0079 a0001c0001t0018g0096 |
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 | a0001c0001t0035g0136 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0044 | 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 | a0001c0001t0007g0066 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | 151 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(148): 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 | |||||||
| chr1:178821972 | G | A | 8 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0012g0038 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0035g0136 | 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0001g0259 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0039g0147 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.480+1420A>G | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 7/19 | chr1 | 178823124 | |||||||
| chr1:178823420 | A | G | 2 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0244 a0001c0001t0001g0247 a0001c0001t0001g0272 |
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 | a0001c0001t0001g0198 | 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0165 a0001c0001t0001g0192 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | 45 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(42): 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 | a0001c0001t0018g0079 a0001c0001t0018g0096 |
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 | a0001c0004t0004g0002 | 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 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0114 others(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 | a0001c0001t0035g0136 | 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 | a0001c0001t0019g0145 a0001c0001t0019g0146 a0001c0001t0035g0136 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0001g0244 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0009g0112 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0002c0005t0038g0041 | 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 | a0001c0001t0001g0154 a0001c0001t0001g0169 a0001c0001t0001g0173 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0271 | 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 | a0001c0001t0002g0099 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0006g0045 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0001t0001g0281 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | 86 | a0001c0001t0001g0154 a0001c0001t0001g0176 a0001c0001t0001g0192 others(83): 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 | a0001c0001t0008g0142 a0001c0001t0012g0038 a0001c0001t0012g0039 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0189 a0001c0001t0006g0042 a0001c0001t0006g0043 others(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 | a0001c0001t0001g0157 a0002c0005t0038g0041 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0046 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0019g0145 a0001c0001t0019g0146 a0001c0001t0035g0136 |
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 | a0001c0001t0031g0179 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0006g0045 a0001c0001t0006g0047 a0001c0001t0006g0048 others(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 | a0001c0001t0006g0047 a0001c0001t0006g0048 a0001c0001t0006g0049 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | 151 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(148): 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0001t0002g0080 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | 22 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(19): 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0006g0045 | 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 | a0002c0005t0038g0041 | 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 | 22 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(19): 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 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(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 | a0001c0001t0006g0044 | 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 | a0001c0002t0005g0035 a0001c0002t0005g0036 |
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 | a0001c0001t0010g0058 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0167 others(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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0002t0005g0129 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0008g0138 | 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0001g0224 | 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 | a0001c0002t0005g0009 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0297 |
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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0008g0139 | 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 | a0001c0001t0001g0051 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | 193 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(190): 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0256 | 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 | a0001c0001t0006g0044 a0001c0001t0008g0137 a0001c0001t0008g0138 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0047 others(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 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0048 others(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 | a0001c0001t0001g0281 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0031g0179 | 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 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0216 others(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 | a0001c0001t0001g0167 | 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 | a0001c0001t0019g0145 a0001c0001t0019g0146 |
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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0035g0136 | 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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0225 a0001c0001t0001g0246 others(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 | a0001c0001t0010g0239 | 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 | a0001c0002t0004g0119 a0001c0002t0004g0120 a0001c0002t0004g0121 others(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 | a0001c0001t0001g0229 | 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 | a0001c0001t0001g0231 a0001c0001t0001g0252 a0001c0001t0001g0303 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0001g0182 | 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 | a0001c0001t0006g0044 | 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 | a0001c0001t0008g0139 | 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 | a0001c0001t0001g0199 | 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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | 152 | a0001c0001t0001g0131 a0001c0001t0001g0176 a0001c0001t0002g0003 others(149): 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 | a0001c0001t0001g0285 | 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 | a0001c0001t0001g0131 a0001c0001t0002g0078 a0001c0001t0002g0080 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | 22 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(19): 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 | a0001c0001t0010g0058 | 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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0009g0116 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | 151 | a0001c0001t0001g0176 a0001c0001t0002g0003 a0001c0001t0002g0004 others(148): 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 | a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0114 others(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 | a0002c0005t0038g0041 | 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 | 49 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0057 others(46): 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0006g0045 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0219 a0001c0001t0001g0229 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0002g0089 a0001c0001t0002g0099 a0001c0001t0002g0135 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | 151 | a0001c0001t0001g0176 a0001c0001t0002g0003 a0001c0001t0002g0004 others(148): 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0019g0145 a0001c0001t0019g0146 |
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 | a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | a0001c0001t0001g0242 a0001c0001t0001g0258 a0001c0001t0001g0261 others(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 | a0001c0001t0002g0088 a0001c0001t0002g0102 a0001c0001t0002g0133 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0047 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | 298 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): 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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0001g0303 | 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 | a0001c0002t0003g0014 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0002t0005g0129 | 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0001g0245 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0216 a0001c0001t0027g0185 |
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 | a0001c0001t0014g0265 a0001c0001t0014g0266 a0001c0001t0014g0274 |
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 | 22 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(19): 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | 152 | a0001c0001t0001g0131 a0001c0001t0001g0176 a0001c0001t0002g0003 others(149): 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 | a0001c0001t0001g0242 a0001c0001t0001g0268 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0028g0155 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0028g0155 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0028g0155 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0028g0155 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0014g0265 a0001c0001t0014g0266 a0001c0001t0014g0274 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0019g0145 a0001c0001t0019g0146 |
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 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0114 others(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 | a0001c0001t0001g0202 | 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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0011g0073 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0252 | 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0002g0083 a0001c0001t0002g0088 a0001c0001t0002g0102 others(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 | a0001c0001t0001g0191 a0001c0001t0001g0208 a0001c0001t0001g0209 others(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 | a0001c0001t0001g0191 a0001c0001t0001g0208 a0001c0001t0001g0209 others(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 | a0001c0001t0001g0191 a0001c0001t0001g0208 a0001c0001t0001g0209 others(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 | a0001c0001t0001g0191 a0001c0001t0001g0208 a0001c0001t0001g0209 others(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 | a0001c0001t0001g0191 a0001c0001t0001g0208 a0001c0001t0001g0209 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0002t0022g0006 | 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 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0114 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0001g0260 a0001c0001t0001g0304 |
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 | a0001c0001t0039g0147 | 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 | 96 | a0001c0001t0001g0176 a0001c0001t0001g0260 a0001c0001t0006g0042 others(93): 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0047 others(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 | 46 | a0001c0001t0001g0176 a0001c0002t0003g0001 a0001c0002t0003g0014 others(43): 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 | a0001c0001t0001g0166 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0002g0107 a0001c0001t0002g0290 a0001c0001t0002g0293 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0177 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0167 others(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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | 1 | a0001c0001t0035g0136 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.607+8677A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 8/19 | chr1 | 178842227 | |||||||
| chr1:178842343 | C | T | 1 | a0001c0001t0035g0136 | 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 | a0001c0001t0039g0147 a0001c0002t0004g0121 a0002c0005t0038g0041 |
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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0001g0218 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0028g0155 | 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 | a0001c0001t0036g0076 a0001c0002t0005g0035 a0001c0002t0005g0036 |
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 | a0001c0001t0036g0076 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0277 | 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 | a0001c0001t0016g0183 | 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 | a0001c0001t0020g0037 | 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 | a0001c0002t0005g0129 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0167 | 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 | a0001c0001t0010g0058 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0002c0005t0038g0041 | 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 | a0001c0001t0002g0107 a0001c0002t0024g0148 |
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 | a0001c0001t0028g0155 a0001c0002t0024g0148 |
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 | a0001c0001t0001g0250 a0001c0001t0002g0286 a0001c0001t0006g0042 others(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 | a0001c0001t0006g0042 | 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 | a0001c0001t0001g0211 a0001c0001t0001g0221 a0001c0001t0012g0038 others(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 | a0001c0001t0001g0188 | 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 | a0001c0001t0002g0085 a0001c0001t0012g0038 a0001c0001t0012g0039 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | 152 | a0001c0001t0001g0131 a0001c0001t0001g0176 a0001c0001t0002g0003 others(149): 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | 203 | a0001c0001t0001g0055 a0001c0001t0001g0131 a0001c0001t0001g0154 others(200): 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 | a0001c0001t0001g0216 a0001c0001t0007g0063 a0001c0001t0007g0064 others(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 | a0001c0001t0020g0005 | 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 | a0001c0001t0001g0055 a0001c0001t0001g0249 a0001c0001t0001g0253 others(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 | 150 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(147): 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 | 81 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(78): 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 | a0001c0001t0001g0164 | 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 | a0001c0002t0003g0031 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0019g0145 a0001c0001t0019g0146 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0178 a0001c0001t0001g0195 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | 150 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(147): 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 | a0001c0002t0005g0010 | 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 | a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | 36 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(33): 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | 148 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(145): 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0001g0216 | 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | a0001c0001t0001g0264 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0283 |
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 | a0001c0001t0034g0093 | 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 | a0001c0002t0004g0128 | 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 | a0001c0001t0001g0186 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0002t0003g0020 a0001c0002t0003g0022 a0001c0002t0003g0030 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0001g0211 a0001c0001t0001g0221 |
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 | a0001c0001t0006g0044 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | 82 | a0001c0001t0001g0176 a0001c0001t0006g0042 a0001c0001t0006g0043 others(79): 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 | 46 | a0001c0001t0001g0176 a0001c0002t0003g0001 a0001c0002t0003g0014 others(43): 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 | a0001c0001t0002g0077 a0001c0001t0036g0076 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0002t0003g0015 a0001c0002t0003g0019 a0001c0002t0003g0020 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0035g0136 | 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0001g0050 a0001c0001t0001g0051 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | 46 | a0001c0001t0001g0176 a0001c0002t0003g0001 a0001c0002t0003g0014 others(43): 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0002t0005g0035 a0001c0002t0005g0036 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0010g0058 | 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 | 200 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(197): 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 | a0001c0001t0001g0262 | 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 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0153 others(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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0131 a0001c0001t0001g0187 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0039g0147 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 |
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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0001g0176 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0002g0077 a0001c0001t0036g0076 a0001c0003t0017g0149 |
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 | a0001c0001t0002g0081 | 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 | a0001c0002t0004g0122 | 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 | a0001c0001t0001g0170 | 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0002g0083 a0001c0001t0002g0134 |
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 | a0001c0001t0019g0145 a0001c0001t0019g0146 |
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 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0047 others(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 | a0001c0001t0001g0282 | 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(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 | 64 | a0001c0001t0002g0082 a0001c0001t0002g0130 a0001c0001t0007g0063 others(61): 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0165 | 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 | a0001c0001t0034g0093 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0039g0147 | 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 | a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0160 a0001c0001t0001g0165 a0001c0001t0001g0191 others(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 | 16 | a0001c0001t0001g0166 a0001c0002t0003g0001 a0001c0002t0003g0014 others(13): 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 | a0001c0002t0004g0121 a0001c0002t0004g0122 a0001c0002t0004g0124 |
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 | a0001c0004t0004g0002 | 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 | a0001c0001t0012g0040 | 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 | a0001c0001t0012g0038 | 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 | a0001c0001t0012g0039 | 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 | a0001c0002t0004g0119 a0001c0002t0004g0120 a0001c0002t0004g0126 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0002t0004g0013 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0008g0137 a0001c0001t0008g0141 a0001c0001t0008g0142 |
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 | a0001c0001t0006g0045 | 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 | a0001c0001t0006g0046 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0008g0137 others(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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0002t0005g0129 | 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 | a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0002t0024g0148 | 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 | a0001c0001t0035g0136 | 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 | a0001c0001t0006g0049 | 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 | a0001c0001t0006g0048 | 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 | a0001c0001t0008g0143 | 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 | a0001c0001t0006g0047 | 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 | a0001c0001t0001g0050 a0001c0001t0001g0191 a0001c0001t0001g0208 others(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 | a0001c0001t0001g0053 a0001c0001t0001g0211 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0299 a0001c0001t0010g0058 a0001c0001t0013g0220 |
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 | a0001c0001t0009g0116 | 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 | a0001c0001t0009g0112 a0001c0001t0009g0118 |
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 | a0001c0001t0009g0117 | 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 | a0001c0001t0009g0111 a0001c0001t0009g0114 |
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 | a0001c0001t0001g0160 a0001c0001t0001g0214 a0001c0001t0001g0284 others(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 | 78 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0054 others(75): Show |
78 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(75): 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 | a0001c0001t0001g0055 a0001c0001t0001g0157 a0001c0001t0001g0159 others(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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0260 a0001c0001t0001g0277 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0059 a0001c0001t0001g0144 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0002t0005g0008 others(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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | a0001c0001t0012g0151 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0002g0080 | 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 | 23 | a0001c0001t0001g0059 a0001c0001t0001g0144 a0001c0001t0001g0191 others(20): Show |
23 | HG00558.hp1 HG00733.hp2 HG01255.hp1 others(20): 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 | a0001c0001t0001g0056 a0001c0001t0001g0221 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0057 a0001c0001t0001g0211 a0001c0001t0001g0232 others(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 | a0001c0001t0001g0262 a0001c0001t0001g0279 a0001c0002t0004g0122 others(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 | a0001c0001t0002g0133 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0002g0080 a0001c0001t0002g0083 a0001c0001t0002g0084 others(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 | a0001c0001t0002g0086 a0001c0001t0002g0088 a0001c0001t0002g0090 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0082 others(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 | a0001c0001t0007g0063 a0001c0001t0019g0145 a0001c0002t0004g0013 |
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 | a0001c0001t0007g0064 a0001c0001t0007g0065 a0001c0001t0019g0146 others(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 | a0001c0001t0002g0077 a0001c0002t0004g0128 |
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 | a0001c0001t0012g0040 | 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 | a0001c0001t0002g0288 a0001c0001t0011g0073 |
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 | a0001c0001t0002g0078 a0001c0001t0011g0067 a0001c0004t0004g0002 |
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 | a0001c0002t0024g0148 | 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 | a0001c0001t0011g0061 a0001c0001t0011g0068 |
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 | a0001c0001t0007g0066 | 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 | a0001c0001t0007g0070 a0001c0001t0011g0069 |
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 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0159 others(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 | a0001c0001t0001g0176 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0008g0140 a0001c0001t0008g0143 a0001c0001t0009g0111 others(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 | 23 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(20): 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0002t0005g0129 | 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 | a0001c0001t0002g0095 a0001c0001t0002g0097 a0001c0001t0002g0098 others(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 | a0001c0001t0002g0286 | 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 | a0001c0001t0002g0081 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0214 | 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 | a0001c0002t0004g0013 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0001g0253 a0001c0001t0001g0300 |
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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 others(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 | a0001c0001t0002g0099 | 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 | 150 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(147): 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | 201 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(198): 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 | a0001c0001t0002g0097 a0001c0001t0002g0098 |
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 | a0001c0001t0001g0177 | 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0002c0005t0038g0041 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0044 | 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 | a0001c0001t0027g0185 | 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 | a0001c0001t0001g0153 | 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 | 150 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(147): 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0002g0084 a0001c0001t0002g0087 a0001c0001t0002g0103 |
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 | a0001c0001t0032g0201 | 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 | 151 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(148): 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 | a0001c0001t0019g0145 | 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 | a0001c0001t0001g0249 | 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 | a0001c0001t0001g0131 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | 29 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0016 others(26): 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 others(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 | 70 | a0001c0001t0001g0056 a0001c0001t0001g0159 a0001c0001t0001g0161 others(67): 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0002g0099 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0039g0147 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0174 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0055 others(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 | 69 | a0001c0001t0001g0050 a0001c0001t0001g0178 a0001c0001t0001g0199 others(66): 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 | a0001c0001t0001g0131 a0001c0001t0001g0169 a0001c0001t0002g0083 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0001g0176 others(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 | 14 | a0001c0001t0001g0052 a0001c0001t0001g0059 a0001c0001t0001g0144 others(11): Show |
14 | HG00558.hp1 HG01243.hp2 HG01257.hp2 others(11): 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 | a0001c0001t0028g0155 a0001c0002t0003g0024 a0001c0002t0016g0029 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0015g0108 a0001c0001t0015g0109 |
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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0131 a0001c0001t0002g0078 a0001c0001t0002g0080 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | 148 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(145): 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | 36 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(33): 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0114 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0039g0147 | 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 | a0001c0001t0001g0301 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0192 a0001c0001t0001g0248 a0001c0001t0001g0277 others(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 | a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | a0001c0001t0028g0155 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0047 a0001c0001t0006g0048 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0010g0254 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
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 | a0001c0002t0004g0013 a0001c0002t0004g0119 a0001c0002t0004g0120 others(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 | a0001c0001t0001g0300 a0001c0001t0002g0081 a0001c0002t0005g0012 others(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 | a0001c0001t0001g0260 a0001c0001t0001g0277 a0001c0001t0001g0282 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0011g0067 a0001c0001t0011g0068 a0001c0001t0011g0069 others(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 | a0001c0001t0001g0260 a0001c0001t0001g0277 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0156 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0162 a0001c0001t0001g0163 others(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 | a0001c0001t0001g0213 | 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 | 101 | a0001c0001t0001g0284 a0001c0001t0002g0003 a0001c0001t0002g0004 others(98): 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 | a0001c0001t0001g0055 a0001c0001t0001g0249 a0001c0001t0001g0253 others(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 | a0001c0001t0001g0215 a0001c0001t0007g0063 a0001c0001t0007g0064 others(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 | a0001c0001t0001g0050 | 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 | a0001c0001t0006g0043 a0001c0001t0006g0044 a0001c0001t0006g0047 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0045 a0001c0001t0006g0046 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0045 a0001c0001t0006g0046 |
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 | a0001c0001t0007g0071 | 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 | a0001c0001t0002g0083 a0001c0001t0002g0088 a0001c0001t0002g0102 others(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 | a0001c0001t0002g0083 a0001c0001t0002g0134 |
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 | a0001c0001t0001g0204 | 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 | 147 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(144): 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0035g0136 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | 150 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(147): 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 | a0001c0001t0001g0182 | 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 | a0001c0001t0002g0088 a0001c0001t0002g0133 |
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 | a0001c0001t0002g0100 | 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 | a0001c0002t0003g0016 a0001c0002t0003g0017 |
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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0002t0005g0129 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0004t0004g0002 | 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 | a0001c0001t0006g0042 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0241 a0001c0001t0001g0259 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0193 | 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 | a0001c0001t0016g0183 | 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 | a0001c0001t0001g0253 a0001c0001t0001g0300 |
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 | a0001c0001t0007g0066 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0001g0131 a0001c0001t0002g0003 a0001c0001t0002g0004 others(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 | a0001c0001t0002g0078 | 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 | a0001c0001t0035g0136 | 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 | 150 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(147): 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 | a0001c0001t0014g0265 | 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 | a0001c0001t0031g0179 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0013g0220 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0175 a0001c0001t0001g0194 a0001c0001t0001g0196 others(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 | a0001c0001t0001g0249 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0164 a0001c0001t0001g0189 |
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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0002g0083 a0001c0001t0002g0134 |
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 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0156 | 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 | a0001c0002t0003g0027 | 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 | a0001c0002t0005g0129 | 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 | a0001c0001t0001g0181 | 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 | a0001c0002t0004g0128 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | 210 | a0001c0001t0001g0055 a0001c0001t0001g0131 a0001c0001t0001g0154 others(207): 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0001g0255 | 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 | a0001c0001t0006g0044 | 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 | a0001c0001t0001g0253 a0001c0001t0001g0300 |
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 | a0001c0001t0001g0221 | 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 | a0001c0002t0005g0008 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0002g0099 | 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 | a0001c0001t0036g0076 | 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 | a0001c0001t0002g0077 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | 45 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(42): 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0002g0132 | 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0027g0185 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0019g0145 a0001c0001t0019g0146 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0218 | 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 | a0001c0001t0010g0058 | 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 | a0001c0001t0010g0058 | 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 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0002t0005g0008 others(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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | 149 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(146): 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 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0002t0003g0014 a0001c0002t0003g0028 a0001c0002t0003g0031 |
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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0036g0076 | 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 | a0001c0002t0005g0008 | 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 | a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0008g0143 | 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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0001g0211 a0001c0001t0001g0221 |
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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0169 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0002g0088 a0001c0001t0002g0102 a0001c0001t0002g0133 others(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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0035g0136 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0028g0155 | 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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0001g0227 a0001c0001t0001g0251 |
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 | a0001c0001t0013g0210 | 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | 45 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(42): 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | 34 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(31): 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 | 36 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(33): 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 | a0001c0001t0019g0145 a0001c0001t0019g0146 |
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 | a0001c0001t0001g0154 a0001c0001t0001g0169 a0001c0001t0001g0173 others(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 | 135 | a0001c0001t0001g0050 a0001c0001t0001g0231 a0001c0001t0001g0285 others(132): 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | 34 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(31): 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 | a0001c0001t0001g0271 | 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 | 81 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(78): 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 | a0001c0001t0002g0077 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0006g0042 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | 1 | a0001c0002t0003g0001 | 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 | a0001c0001t0002g0081 | 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 | a0002c0005t0038g0041 | 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 | a0001c0001t0014g0265 a0001c0001t0014g0266 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0218 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | 80 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(77): 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0006g0046 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | 44 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(41): 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 | a0001c0001t0001g0227 a0001c0001t0001g0251 |
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 | a0001c0001t0002g0288 | 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 | a0001c0001t0002g0095 a0001c0001t0002g0097 a0001c0001t0002g0098 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0245 | 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 | a0001c0002t0004g0013 a0001c0002t0004g0128 |
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 | a0001c0001t0006g0042 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0281 | 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0028g0155 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | 254 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(252): 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | 200 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(197): 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 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0196 a0001c0001t0026g0171 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0001g0302 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 others(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 | a0001c0001t0008g0143 | 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 | a0001c0001t0016g0183 | 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 | 1 | a0001c0002t0003g0001 | 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 | a0001c0001t0002g0078 | 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 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0002g0287 | 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 | a0001c0002t0004g0128 | 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 | a0001c0001t0019g0145 a0001c0001t0019g0146 a0001c0001t0035g0136 |
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 | |||||||
| chr1:178888013 | T | G | 1 | a0001c0001t0002g0078 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0273 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0002g0089 a0001c0001t0002g0099 a0001c0001t0002g0135 |
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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0011g0061 a0001c0001t0011g0062 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | 154 | a0001c0001t0001g0055 a0001c0001t0001g0249 a0001c0001t0001g0253 others(151): 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 | 154 | a0001c0001t0001g0055 a0001c0001t0001g0249 a0001c0001t0001g0253 others(151): 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 | a0001c0001t0006g0044 | 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 | a0001c0001t0002g0288 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0002t0004g0119 a0001c0002t0004g0120 a0001c0002t0004g0121 others(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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0006g0047 a0001c0001t0006g0048 a0001c0001t0006g0049 others(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 | |||||||
| chr1:178890476 | C | T | 1 | a0001c0001t0001g0230 | 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 | a0001c0001t0002g0083 a0001c0001t0002g0134 |
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 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0114 others(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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0114 others(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 | a0001c0001t0001g0222 a0001c0001t0001g0237 a0001c0001t0001g0238 |
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 | a0001c0001t0035g0136 | 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 | 155 | a0001c0001t0001g0055 a0001c0001t0001g0249 a0001c0001t0001g0253 others(152): 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0002g0289 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
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 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | 48 | a0001c0001t0001g0055 a0001c0001t0001g0249 a0001c0001t0001g0253 others(45): 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0002g0152 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | 84 | a0001c0001t0001g0055 a0001c0001t0001g0144 a0001c0001t0001g0249 others(81): 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 others(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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0001t0002g0080 | 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 | a0001c0001t0001g0250 | 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 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0216 |
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 | 13 | a0001c0001t0001g0197 a0001c0001t0001g0255 a0001c0001t0001g0277 others(10): Show |
13 | HG00738.hp2 HG01070.hp2 HG01071.hp2 others(10): 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 | a0001c0001t0001g0297 a0001c0001t0001g0300 a0001c0001t0002g0105 others(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 | a0001c0001t0002g0130 | 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0002g0110 a0001c0001t0002g0287 a0001c0001t0002g0295 others(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 | 43 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(40): 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 | a0001c0001t0001g0059 a0001c0001t0001g0205 a0001c0001t0001g0208 others(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 | 48 | a0001c0001t0001g0055 a0001c0001t0001g0249 a0001c0001t0001g0253 others(45): 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 | a0001c0001t0001g0249 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0002g0077 a0001c0001t0036g0076 |
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 | a0001c0001t0001g0273 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0002g0113 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0007g0066 a0001c0001t0007g0070 a0001c0001t0007g0072 |
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 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0114 others(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 | a0001c0001t0001g0261 | 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 | a0001c0001t0002g0115 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0267 a0001c0002t0005g0129 |
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 | a0001c0001t0035g0136 | 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 | a0001c0002t0024g0148 | 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 | 150 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(147): 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0001g0059 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 |
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 | a0001c0001t0001g0231 | 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0019g0145 a0001c0001t0019g0146 a0001c0001t0035g0136 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0014g0274 a0001c0001t0028g0155 |
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 | a0001c0001t0001g0282 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0002t0004g0013 | 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 | a0001c0001t0002g0082 | 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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0001t0037g0291 | 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 | a0001c0001t0002g0132 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 others(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 | a0001c0001t0001g0131 a0001c0001t0001g0187 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0019g0145 a0001c0001t0019g0146 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0002t0016g0029 | 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0175 a0001c0001t0001g0194 a0001c0001t0001g0196 others(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 | a0001c0001t0006g0046 | 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 | a0001c0001t0035g0136 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0002g0152 | 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 | a0001c0001t0001g0054 a0001c0001t0001g0195 a0001c0001t0001g0224 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0002t0003g0014 a0001c0002t0003g0030 a0001c0002t0004g0013 others(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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0040 a0001c0001t0021g0074 |
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 | 67 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(64): 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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | 57 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(54): 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0001g0196 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0001t0001g0170 | 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 | a0001c0001t0001g0281 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0002g0288 | 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | 42 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(39): 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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 others(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 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0047 others(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 | 80 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(77): 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 | a0001c0001t0001g0209 | 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | 42 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(39): 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0193 a0001c0001t0001g0219 a0001c0001t0001g0229 |
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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | 200 | a0001c0001t0001g0055 a0001c0001t0001g0154 a0001c0001t0001g0157 others(197): 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 | 35 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(32): 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 | a0001c0001t0010g0239 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0002g0289 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0114 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0153 others(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 | a0001c0002t0022g0006 a0001c0002t0022g0007 |
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 | a0001c0001t0006g0045 a0001c0001t0006g0046 a0001c0001t0006g0047 others(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 | 149 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(146): 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 | a0001c0001t0001g0255 | 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 | a0001c0001t0039g0147 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0028g0155 | 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 | 80 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(77): 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0001g0250 | 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 | a0001c0001t0014g0265 a0001c0001t0014g0266 a0001c0001t0014g0274 |
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 | a0001c0001t0010g0058 | 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 | a0001c0001t0002g0130 a0001c0001t0008g0137 a0001c0001t0008g0138 others(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 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0114 others(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 | a0001c0002t0016g0029 | 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 | a0001c0002t0016g0029 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0010g0257 | 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0006g0047 | 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 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0002g0092 others(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 | a0001c0001t0011g0067 | 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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | 21 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(18): 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0004t0004g0002 | 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 | a0001c0001t0001g0181 | 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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0001g0199 | 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 | a0001c0001t0002g0115 | 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 | a0001c0001t0035g0136 | 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 | a0001c0001t0002g0133 | 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 | a0001c0001t0002g0133 | 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0019g0145 a0001c0001t0019g0146 |
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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0002t0004g0128 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0010g0239 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0056 a0001c0001t0001g0057 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0158 a0001c0001t0001g0223 others(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 | 42 | a0001c0001t0002g0134 a0001c0001t0008g0137 a0001c0001t0008g0138 others(39): 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0002t0005g0008 a0001c0002t0005g0009 a0001c0002t0005g0010 others(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 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | 44 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(41): 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 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0077 others(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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0032g0201 | 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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | 35 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(32): 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0027g0185 | 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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0001g0261 | 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 | a0001c0001t0002g0077 a0001c0001t0036g0076 |
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 | a0001c0001t0008g0137 a0001c0001t0008g0138 a0001c0001t0008g0139 others(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 | a0001c0001t0001g0261 | 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 | a0001c0001t0006g0044 | 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 | a0001c0001t0006g0045 | 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 | a0001c0002t0005g0035 a0001c0002t0005g0036 |
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 | 42 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(39): 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 | a0001c0003t0017g0149 a0001c0003t0017g0150 |
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 | a0001c0001t0001g0263 a0001c0001t0001g0279 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 a0001c0003t0017g0149 others(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 | a0001c0001t0001g0188 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0001g0216 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | 1 | a0001c0002t0003g0001 | 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 | a0001c0001t0001g0227 a0001c0001t0001g0251 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | 1 | a0001c0002t0003g0001 | 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 | a0001c0001t0001g0214 a0001c0001t0001g0284 |
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 | a0001c0001t0012g0151 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0002g0115 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0001g0178 a0001c0001t0001g0227 a0001c0001t0001g0251 others(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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0001g0158 | 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 | a0001c0001t0002g0078 | 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 | a0001c0002t0003g0016 a0001c0002t0003g0017 a0001c0002t0003g0026 others(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 | a0001c0001t0012g0038 a0001c0001t0012g0039 a0001c0001t0012g0040 others(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 | a0001c0001t0001g0267 | 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 | a0001c0001t0039g0147 a0002c0005t0038g0041 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0011g0073 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
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 | a0001c0001t0006g0042 a0001c0001t0006g0043 a0001c0001t0006g0044 others(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 | a0001c0001t0002g0088 a0001c0001t0002g0102 a0001c0001t0002g0133 others(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 | a0001c0001t0001g0170 | 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 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0065 others(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 | a0001c0001t0012g0151 a0001c0001t0021g0074 a0001c0001t0021g0075 |
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 | a0001c0001t0001g0193 a0001c0001t0001g0219 a0001c0001t0001g0229 |
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 | 42 | a0001c0002t0003g0001 a0001c0002t0003g0014 a0001c0002t0003g0015 others(39): 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 | 298 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(295): Show |
299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): 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 | a0001c0001t0001g0195 | 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 | a0001c0004t0004g0002 | 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 | a0001c0001t0020g0005 a0001c0001t0020g0037 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1723-512A>C | RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 19/19 | chr1 | 178915818 |